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Table of Content

    2013, Volume 44 Issue 2
    06 April 2013
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    β-amyloid protein induces the changes of astrocytic N-methyl-D-aspartate receptor subunits expression in rat hippocampus
    GAO Xiang-hong SONG Yi-zhi CHANG Li-rong ZHANG Ya-li WU Yan* 
    2013, 44 (2 ):  146-151.  doi: 10.3969/j.issn.0529-1356.2013.02.001
    Abstract ( )  

    Objective To investigate the effects of β-amyloid protein (Aβ25-35) on astrocytic N-methyl-D-aspartate receptor (NMDAR) subunits in the rat hippocampus. Methods Aβ25-35 (10μmol/L) was added into the primary cultured hippocampal cells for 1 hour and 24 hours. Immunofluorescence technique was applied to investigate the changes of the expression of NR1, NR2A and NR2B between the control group and Aβ groups ( n =10). Results NR1, NR2A and NR2B were expressed in the hippocampal astrocytes.The positive puncta were mainly distributed in the soma and process. The expression was intensive in the soma and scattered in the process. Their expression was increased following Aβ25-35treatment ( P <0.05 vs control group). The expression of NR2A and NR2B were significantly increased ( P <0.05) between Aβ 1hour group and Aβ 24hours group, while there was no significant changes in NR1 group. Conclusion The rat hippocampal astrocytes express NMDAR subunits (NR1, NR2A and NR2B), and their expressions are significantly increased after Aβ25-35treatment, while the variation tendency of NR1 is different from the changes of NR2A and NR2B.

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    Ischemic postconditioning prevents cytochrome C release through up-regulation of p-Akt and protects neurons against ischemia insult 
    ZHANG Li-zhu ZHOU Cai-feng TU Jing-yi ZHANG Xi ZHU Ying WANG Rui-min* 
    2013, 44 (2 ):  152-156.  doi: 10.3969/j.issn.0529-1356.2013.02.002
    Abstract ( )  

    Objective The goal of this study is to elucidate the neuro-protective effect and the possible mechanism of delayed ischemic postconditioning through observing the level of p-Akt and cytochrome C (Cyt C) in cytoplasm or mitochondria following global cerebral ischemia. Methods 40 Adult male Sprague-Dawley rats were subjected to global cerebral ischemia by four-vessel occlusion and were randomly divided into five groups: sham group, ischemia-reperfusion group (I/R), delayed ischemic postconditioning group (Post C), Vehicle group (Post C+Vehicle) and LY294002 group (Post C+LY294002). Cresyl violet staining was used to observe the surviving neurons of hippocampal CA1 region following global cerebral ischemia and western blot analysis was used to detect the level of p-Akt and Cyt C in both cytosolic and mitochondrial fraction. Results Delayed ischemic postconditioning protected the hippocampal CA1 region neurons against ischemia/referfusion injury and significantly increased the level of p-Akt in cytoplasm compared with I/R groups. Delayed ischemic postconditioning markedly prevented the release of Cyt C from mitochondria to cytoplasm and LY294002, an inhibitor of Akt up-stream kinase, abolished the positive role of delayed ischemic postconditioning. Conclusion Delayed ischemic postconditioning induces the Akt activation and prevents the release of Cyt C from mitochondria to cytoplasm, thereby blocks the hippocampal CA1 region neurons injury following global cerebral ischemia.

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    Prenatal nicotine exposure induces adult offspring high response to central angiotensin II
    YU Feng ZHANG Jian-guo GAO Xi-ren DONG Wei-jia ZHANG Zhi-zhi ZHANG Bo XIA Zhi-heng ZHANG Yu-juan * 
    2013, 44 (2 ):  157-162.  doi: 10.3969/j.issn.0529-1356.2013.02.003
    Abstract ( )  

    Objective To investigate the effect of prenatal nicotine exposure to the adult offspring response to central angiotensin. Methods The mean arterial pressure(MAP) and blood gas analysis after intracerebroventricular (ICV)injection of angiotensin II(AngII), losartan(Los), PD123319(PD)to nicotine offspring (nicotine, n =7)and control offspring(control, n =7) were tested. The angiotensin Ⅱ receptor 1 (AT1aR), AT1bR and AT2R mRNA, c-Fos protein, and AT1R, AT2R protein expression of anterior hypothalamic area(AHA) were detected. Results There was no difference between the control and nicotine groups, but after ICV AngII, the MAP was significantly higher in nicotine group than in the control group [(120.36±6.23)mmHg vs (109.87±6.86)mmHg,P <0.05]. ICV Los in advance blocked the effect whereas ICV PD did not. The c-Fos expression was stronger in the nicotine group than that in the control group(25.8±2.91 vs 6.42±1.52, P< 0.05). The AT1aR mRNA(1.23±0.05 vs 1.00,P < 0.05)and AT1R protein(0.581±0.06 vs 0.353±0.05,P <0.05)expression were higher in the nicotine group than that in the control group. Conclusion Prenatal nicotine exposure induces higher expression of AT1aR mRNA and AT1R protein, which may result in high response to central angiotensin II of adult offspring.

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    Granulocyte-colony stimulating factor ameliorates periventricular white matter damage subject to hypoxia via influencing on activation of microglia
    DU Yang YAO Lin-li YANG Yang GAO Ming HAO Ai-jun* 
    2013, 44 (2 ):  163-169.  doi: 10.3969/j.issn.0529-1356.2013.02.004
    Abstract ( )  

    Objective To explore the protective effect of granulocyte colony stimulating factor (G-CSF) on the activation of microglial in periventricular white matter damage (PWMD) model mice. Methods One-day old newborn mice(n =108)were randomly divided into control group, injury group and treated group. PWMD model was produced by the hypoxia box in the injury group and treated group. Two hours later, the survived mice in the treated group accepted an intraperitoneal injection of rhG-CSF, continued for 7 days. Some mice in 3 groups were sacrificed on day 1, day 3 and day 7 after treatment. The whole brain of the rat was taken for histological analysis and immunofluorescence to observe the accumulation of microglia in vivo and the secretion of cytokines. The periventricular white matter was collected using enzyme-linked immunosorbent assay (ELISA) to detect the level of inflammatory cytokine secretion. The secretion of proinflammatory cytokines and suppression of inflammatory cytokines as well as two types of activated microglia in the number and proportion changes were detected by RT-PCR. The injections of rhG-CSF was finished on day 7 and the neurobehavioral experiments began on day 5, 8, 10, 12 and 30, respectively. The changes of their muscle tone, voluntary movement, and emotional behavior were observed. Results G-CSF facilitated the recruitment of microglia, changed the number and proportion of the M1 and M2 cells in activated microglia, and decreased proinflammatory cytokine secretion as well as increasing the neurotrophic factor secretion. In addition, the recovery of muscle tone, voluntary movement, and sense and motor fuctions were promoted by G-CSF. Conclusion In this study, the administration of G-CSF in the periventricular white matter injury accelerated mouse motor function recovery, improved cerebral palsy symptoms, led the microglia altering to neural protection, and regulated the secretion of inflammatory factors and neurotrophic factors.

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    Influence of intrathecal siRNA of postsynaptic density protein 95 on CaMKⅡα activation in spinal cord of rats with neuropathic pain
    XU Li YU Jie SHEN Le LI Xu HUANG Yu-guang* 
    2013, 44 (2 ):  170-175.  doi: 10.3969/j.issn.0529-1356.2013.02.005
    Abstract ( )  

    Objective To explore the influence of intrathecal postsynaptic density protein 95(PSD-95) gene specific siRNAs on CaMKⅡα phosphorylation in spinal cord of rats with neropathic pain. Methods The NG108-15 neuroal cells were transfected with chemically synthesized siRNA targeting PSD-95 for comprehensive evaluation of its silence efficacy. Ninety-one adult male Sprague-Dawley rats were randomly divided into three groups: naive, sham and sciatic nerve chronic constriction injury (CCI) group. All the rats in CCI group were subdivided into four groups, which were treated with normal saline(control group), transfection vehicle(vehicle group), mismatch siRNAs(mmRNA group)and PSD-95 gene specific siRNAs(siRNA group)respectively. All the subgroup received corresponding agents intrathecally for 3 days, as was started 5 days after the chronic constriction injury of sciatic nerve. Mechanical withdrawal threshold (MWT) was measured on post intrathecal infusion day 1, 3 and 7 by a series of von Frey hairs. The rats were sacrificed at different times after intrathecal infusion to examine PSD-95 and phosphorylation of CaMKⅡα in the lumber 4-6 spinal cord by Western blotting. Results The siRNAs, which was exclusively identical to PSD-95, decreased PSD-95 level significantly in NG108-15 cells. The MWT of neuropathic pain rats increased significantly after intrethecal administration of PSD-95 specific siRNA ( P <0.05), compared with intrethecal injection of saline. Total CaMKⅡα level did not change after PSD-95 siRNA infusion( P >0.05), however, the pThr286 CaMKⅡα level on the spinal cord of the CCI rats decreased significantly ( P <0.05). Conclusion Administration of PSD-95 gene specific siRNAs attenuates the phosphorylation of CaMKⅡα Thr286 and central sensitization signaling cascades and results in the relief of neuropathic pain.

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    Effect of allopregnanolone on the dopaminergic neurons in the substantia nigra of Alzheimer’s disease mice 
    WANG Qiong-sa, QI Shuang-shuang, ZHOU Peng, ZHANG Chi-hao, CUI Huai-rui, CHEN Shi-xin, SUN Chen-you*
    2013, 44 (2 ):  176-181.  doi: 10.3969/j.issn.0529-1356.2013.02.006
    Abstract ( )  

    Objective The present study was undertaken to evaluate the effects of allopregnanolone (APα) on neurogenesis of dopaminergic neurons by analyzing the numbers of dopaminergic neurons and newly formed dopaminergic neurons in the substantia nigra pars compacta (SNpc) of Alzheimer’s disease (AD) mice. Methods Experiments were performed using 3-month-old male double transgenic amyloid precursor protein with presenilin (APP/PS1) mouse model of AD (2xTg-AD) and non-transgenic (non-Tg) background mice. These mice were administered with APα or phosphate buffer saline (PBS), respectively. Following 24 days, six mice in each group were performed behavior testing by open-field test. The brain tissue from another 6 mice in each group was taken out and post-fixed and the numbers of tyrosine hydroxylase (TH) expressing dopaminergic neurons and TH expression were observed and analyzed in the SNpc region by the immunohistochemistry, unbiased stereology and optical intensity. In addition, the numbers of TH/bromodeoxyuridine (BrdU) double labeled dopaminergic neurons were counted by the immunofluorescent method. Results As compared with the Non-Tg+PBS mice, the data for 2xTg-AD+PBS mice were obviously decreased in the ambulation of open-field test (P <0.01), the intensities of TH immunohistochemical activity (P <0.05), the numbers of dopaminergic neurons and BrdU/TH double labeled neurons in the SNpc regions (P <0.05). As compared with the 2xTg-AD+PBS mice, the data for 2xTg-AD+APα mice was obviously increased in the ambulation of openfield test (P <0.05), the numbers of dopaminergic neurons ( P <0.05) and BrdU/TH double labeled neurons in the SNpc regions ( P <0.01). However, the intensities of TH immunohistochemical activity didn’t alter significantly between the 2xTg-AD+PBS and 2xTg-AD+APα mice (P>0.05). Conclusion These results indicate that APα may ameliorate the loss of numbers of dopaminergic neurons by increasing the numbers of newly formed dopaminergic neurons in the SNpc of 2xTg-AD mice. These results suggest the APα may have a potential therapeutic efficacy in neurogenesis.

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    Curcumin ameliorates the learning and memory of senescence-accelerated mouse and its possible mechanism
    ZHANG Chi-hao QI Shuang-shuang ZHOU Peng WAN Qiong-sa CUI Huai-rui CHEN Shi-xin SUN Chen-you* 
    2013, 44 (2 ):  182-188.  doi: 10.3969/j.issn.0529-1356.2013.02.007
    Abstract ( )  

    Objective The present study is to evaluate the effects of curcumin on the learning and memory of senescence-accelerated mouse prone 8 (SAMP8) and possible mechanisms by analyzing the p-calcium/calmodulin-dependent kinase II (p-CaMKII) expression in the hippocampus. Methods Experiments were performed using 6-month-old male SAMP8 and senescence-accelerated-resistant strain mice (SAMR1). SAMP8 mice were intragastrically administered curcumin at a dose of 20 or 50 mg/kg body weight or fed the same amount of corn oil (SAMP8 treated with vehicle), once a day for 25 consecutive days. Six mice in each group were performed behavior testing by Morris water maze at day 26 (D26) after treatment. The left side of hippocampus from other 6 mice in each group was homogenized and p-CaMKII expressions in hippocampal membrane fraction were measured by Western blotting. The right side of hippocampus was post-fixed and the distribution and expression of p-CaMKII were observed and analyzed in the hippocampal CA3 region by the immunohistochemistry and optical intensity. Results Treatment of curcumin [20 and 50 mg/(kg •d) i. g.] significantly reduced the escape latencies of SAMP8 treated with vehicle (P <0.05, P<0.01) in Morris water maze task. SAMP8 treated with 50 mg/kg of curcumin had a much more time swimming in the target quadrant ( P <0.05). In addition, 50 mg/kg of curcumin obviously increased the intensity of p-CaMKII in the stratum lucidum of hippocampal CA3, and relative protein level for p-CaMKII/ GADPH in the hippocampal membrane fraction as well. Conclusion The curcumin treatment may attenuate cognitive deficits of SAMP8 mice in a dose-dependent effect by improving the expression of p-CaMKII in the hippocampus. Thus treatment with curcumin may have a potential therapeutic effect for aging-related cognitive dysfunctions.

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    Oxidation low density lipoprotein promotes aging of mouse hematopoietic stem cells through regulating cell cycles
    ZHANG Xian-ping ZHANG Gui-hai WEN Kun-ming LIU Jun XU Chu-yan WANG Lu JIANG Rong WANG Ya-ping*
    2013, 44 (2 ):  189-193.  doi: 10.3969/j.issn.0529-1356.2013.02.008
    Abstract ( )  

    Objective To observe the effect of oxidation low density lipoprotein on aging of hematopoietic stem cells (HSCs) and to reveal the underlying mechanisms that ox-LDL induce the aging of HSCs. Method Mouse HSCs were isolated by magnetic cell sorting with Sca-1 staining. Sca-1+ HSCs were cultured with ox-LDL. Senescence-associated β-galactos idase (Saβ-Gal) staining was used to identify aging HSCs. The capacity of self-renewal of HSCs was evaluated by MTS assay. CFU-Mix cultivation was used to evaluate the potency of differentiation in HSCs. Cell cycles were detected by flow cytometry. The expressions of p16, p21, CDK4 and cyclinD were determined by realtime quantitative PCR (qRT-PCR) and Western blotting analysis. Results Exogenous ox-LDL significantly increased the number of Saβ-Gal staining postive in HSCs, promoted HSCs to arrest at S stage, elevated the ratio of G0/G1 stage , decreased the ratio of S stage and the number of CFU-Mix, and inhibited the proliferation of HSCs compared to HSCs without ox-LDL treatment group. Ox-LDLremarkedly upregulated the expression of p16 and p21 in mRNA and protein levels, decreased the protein expression of CDK4 and cyclinD. There was no significant difference in the protein expression of CDK2 in HSCs. Conclusion ox-LDL may induce mice HSCs aging through upregulating the expressions of p16 and p21, and downregulating CDK4 and cyclinD expressions.

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    Autophagic changes of the endothelial progenitor cells carried with fibrin glue after transplantation into the infracted myocardium
    ZHANG Dan WANG Hai-jie* TAN Yu-zhen WANG Qiang-li WU Jin-hong LI Zhi-hua Quan Zhe 
    2013, 44 (2 ):  194-198.  doi: 10.3969/j.issn.0529-1356.2013.02.009
    Abstract ( )  

    Objective To investigate autophagic changes endothelial progenitor cells (EPCs) carried with fibrin glue after transplantation into the infracted myocardial and to explore effects of autophagy on maintaining the implanted cells to survive and fibrin on protecting the cells. Methods The model of myocardial infarction was established with ligating the anterior descending branch of the left coronary artery of rats. The EPCs sorted from human umbilical cord blood were injected into the myocardium at the normal region, periphery of the infarcted region and infarcted region. After transplantation for two hours, the tissues at injection sites were removed, the semithin sections were prepared. Distribution of the EPCs carried with fibrin glue were examined. After positioning the implanted cells, the ultrathin sections were prepared. The changes of the autophagic structures in EPCs and compatibility of fibrin with EPCs and myocardium were evaluated. Results Compared with the normal region, the autophagic EPCs in the periphery of the infarcted region increased, and the autophagic structures in the cells increased. In the infarcted region, EPC autophagy enhanced significantly, and necrosis or apoptosis occurred in some cells. Compatibility of fibrin with EPCs and myocardium was good. The implanted cells in fibrin glue extended well, some EPCs adhered to cardiaomyocytes. Conclusion When EPCs are transplanted into the periphery of the infarcted region, mild ischemia induces autophagy of the cells, which is beneficial for maintaining survival of the transplanted cells. Carrying EPCs with fibrin glue may avoid of cell lose and promote cell survival.

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    Establishment of a simian virus 40 T antigen transfected human umbilical vein endothelial cell line PUMC-HUVEC-T1
    FENG Hai-liang WANG Chun-jing GU Bei YANG Zhen-li LIU Yu-qin*
    2013, 44 (2 ):  199-203.  doi: 10.3969/j.issn.0529-1356.2013.02.010
    Abstract ( )  

    Objective To establish a simian virus 40(SV40)T antigen transfected human umbilical vein endothelial cells (HVUEC) model for endothelial research.Methods Primary human umbilical vein endothelial cells were separated and infected with SV40 large T and small T antigen, and then continuously sub-cultured in vitro. The infected HUVEC of large T expression was detected by RT-PCR. vWF, CD31, CD34 expression and lectin binding were determined by immuno-cytochemistry. Ultra-structure was observed by transmission electron microscopy and the formation of endothelial tubes was accessed by Matrigel.The karyotype was analyzed and tumorigenicity was detected by subcutaneous inoculation in BABL/c nude mice. Mycoplasma and species were checked by PCR. Short tandem repeat(STR) profiling was employed for cell identity.Results The SV40 T antigen transfected cell line was designated as PUMC-HUVEC-T1 and had SV40 LT mRNA expression. The cells were passaged (1∶3-4) for more than 40 times in vitro. Morphologically PUMC-HUVEC-T1 arrayed like pitching stone when reaching confluency. PUMC-HUVEC-T1 showed positive expression of vWF, CD31, CD34, and could bind lectin in vitro. WP corpuscles were identified by electron microscopy. The cells formed vascular network-like structures when planted and cultured on Matrigel. The karyotype was nomal and stable between different passages. No tumor formed in BABL/c-nude mice. PUMC-HUVEC-T1 was conformed of its human origin and its STR was consistent with that of the original HUVEC. No mycoplasma was detected. Conclusion A SV40 T antigen transformed HUVEC cell line PUMC-HUVEC-T1 was successfully established which is accessible with clear background and reliable quality. It would provide a solid base for the endothelial research. It is deposited by cell resource center and is available for distribution.

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    Lactic acid inhibits lipopolysaccharide-induced translocation of NF-κB p65 from cytoplasm to nucleus and transcription of nuclear factor-κB p65 and cyclooxygenase 2
    JIANG Jin-qi XU Guang-yong SHI Ya-ran QIAO Yu HU Ge1 REN Xiao-min*
    2013, 44 (2 ):  204-209.  doi: 10.3969/j.issn.0529-1356.2013.02.011
    Abstract ( )  

    Objective To investigate whether lactic acid(LA),which was extracted from the culture supernatant of Lactobacillus,could inhibit lipopolysaccharide(LPS)-induced translocation of NF-κB p65 from cytoplasm to nucleus and transcription of NF-κB p65 and cyclooxygenase 2(COX-2). Methods Rat intestinal mucosa microvascular endothelial cells(RIMMVEs) were cultured in vitro and were divided into 4 groups:control group,LPS group,LA pretreated group and NF-κB inhibitor (pyrrolidinecarbodithioate,PDTC) pretreated group.The protein of NF-κB p65 in cytoplasm and in nucleus was detected by Western blotting analysis after RIMMVEs were treated with LPS for 30 minutes.The mRNA of NF-κB p65 and COX-2 was detected by real time quantity-PCR after RIMMVEs were treated with LPS for 9 hours. Results In a short time(treated with LPS for 30 minutes),the protein expression of NF-κB p65 had no notable difference but the ratios of p65 in nuclei of LA and PDTC pretreated group were notably lower than that of LPS group.After a longer time(treated with LPS for 9 hours),the mRNA expression of NF-κB p65 and COX-2 were notably lower than LPS group. Conclusion LA has the effects like NF-κB inhibitor,notably inhibiting LPS-induced translocation of NF-κB p65 from cytoplasm to nucleus and transcription of NF-κB p65 and COX-2.By this way,LA inhibits inflammatory response.

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    Effects of curcumin on the expression of Bcl-2 and Bax in rat thoracic aortic aneurysm
    FAN Jun BAI Shu-ling* TIAN Xiao-hong HOU Wei-jian YAN Ya-wei TONG Hao 
    2013, 44 (2 ):  210-213.  doi: 10.3969/j.issn.0529-1356.2013.02.012
    Abstract ( )  

    Objective Curcumin can suppress the development of abdominal aortic aneurysms by inhibiting inammation. The objective of this study is to investigate the effect of curcumin on the expression of Bcl-2 and Bax during rat thoracic aortic aneurysm formation. Methods Thirty adult male Wistar rats were randomly divided into three groups: control group, aneurysmal group and curcumin group. The thoracic aortic aneurysm model induced by CaCl2 was made, followed by daily oral gavage with 100 mg/kg curcumin or vehicle alone. The thoracic aortic segments were collected at 4 weeks after surgery. HE staining and orcein staining were used to observe the histological changes in the thoracic aorta. Immunohistochemistry and Western blotting were performed to detect the expressions of Bcl-2 and Bax in the wall of aneurysm. Results Curcumin significantly inhibited CaCl2 -induced expansion of thoracic aorta, along with structural preservation of medial elastin fibers. Compared with the control group, the expression of Bax was higher, and the expression level of Bcl-2 was lower in the aneurysm group. Curcumin effectively reduced the expression of Bax, and increased Bcl-2 expression level in the aneurysm. Conclusion Our study shows that curcumin can promote the expression of Bcl-2 protein, inhibit the expression of Bax protein, and decrease the ratio of Bax/Bcl-2 in thoracic aortic aneurysms.

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    Overexpression of mitochondrial ferritin inhibited the tumour cell proliferation by regulation of cellular iron mechanism and the expression of cyclins
    SHI Fang-fang ZHANG Na GUAN Peng GAO Zhi-guo FAN Jing-qi CHANG Yan-zhong SHI Zhen-hua* DUAN Xiang-lin 
    2013, 44 (2 ):  214-218.  doi: 10.3969/j.issn.0529-1356.2013.02.013
    Abstract ( )  

    Objective  To study the mechanism of overexpression of mitochondrial ferritin(MtFt) for inhibiting neuroblastoma cell proliferation. Method MtFt-SY5Y cells were selected as the experimental model and SH-SY5Y and pcDNA3.1-SY5Y cells were used as control group. The effects of overexpression of MtFt on SH-SY5Y cells proliferation, iron metabolism related protein transferrin receptor1(TfR1) and ferritin, cyclins(cyclinD1, cyclinE ) and cyclin dependant kinases (CDK2, CDK4) were tested by flow cytometry and Western bloting. Result Overexpression of MtFt inhibited markedly tumour cell proliferation by regulation of iron metabolism and the expression of cyclins and cyclin dependant kinase. The proliferation speed of MtFt-SY5Y cells was 4 times slower than that of the control group. MtFt caused the cytoplasm iron deficiency and transferrin receptor1(TfR1) upregulation, and H-ferritin downregulation markedly respectively. Meanwhile, cyclinD1 and CDK2 downregulated significantly and cyclinE upregulated significantly. The expression of CDK4 decreased but no significant difference compared with control group. Conclusion Overexpression of MtFt inhibits the tumour cell proliferation markedly. The mechanism may be caused by regulation of cellular iron metabosism and the expression of cyclins and cyclin dependent kinase (CDK) which further arrest cell cycle.

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    Effects of gastrin on Reg I gene transcription factors in SGC7901 cell
    WU Yan-fang GUO Lin-xia LE Xiao-ping DING Yi*
    2013, 44 (2 ):  219-223.  doi: 10.3969/j.issn.0529-1356.2013.02.014
    Abstract ( )  

    Objective  To study the effects of gastrin on regenerating gene I(Reg I) gene transcription factors (TFs) in gastric cancer cell SGC7901. Methods  Reg I gene promoter 1414bp fragment was amplified from gastric cancer cell SGC7901 genomic DNA by nest-PCR. The fragment was inserted into PMD19-T vector and identified by sequencing. The 1414bp fragment and its HindⅢ digestion 800bp and 614bp fragments were digoxin-labeled by random primer assay. After sensitivity detection, the three fragments were used as probes. Transcription factor binding sites (TFBS) in Reg I gene promoter 1414bp fragment were analyzed by online software Genomatix MatInspector. Gastric cancer cell SGC7901 was incubated with gastrin-G17 for 48 hours at final concentrations of 10 -7 mol/L and 10 -8 mol/L, and the nuclear proteins were extracted, respectively. Effects of gastrin on Reg I gene TFs were detected by Southwestern blotting using digoxinlabeled 1414bp, 800bp and 614bp as probes, respectively. Results Twenty major bands of proteins with different molecular weight were detected with 1414bp probe. After treatment with gastrin, the pattern of bands showed no change. However, the densities of some bands were changed, the densities of band 9, 12, 13, 14, 15 and 16 decreased significantly ( P<0.05). The densities of 6 bands above mentioned between those in the two groups treated with gastrin at different final concentration had no significant difference ( P >0.05). Of the 6 changed bands detected with 1414bp probe, three bands including band 9, 12 and 13 were detected with proximal 614bp probe. The densities of the three bands also decreased after gastrin incubation ( P<0.05). Three bands including band 9, 12 and 14 detected with distal 800bp probe. However, only the densities of band 14 decreased after gastrin incubation ( P<0.05). Band 15 and band 16 were not detected with proximal 614bp or distal 800bp probe. Conclusion The results suggest that Reg I gene may be transcriptionally regulated by cooperation of many TFs in gastric cancer cell SGC7901. Decreasing binding activities of some TFs may be one of pathways of gastrin up-regulating Reg I gene expression in gastric cancer cell SGC7901.

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    Discordance of aldehyde dehydrogenase 1 and estrogen Receptor expression between primary and metastatic focuses of breast cancer
    SHAO Jun PAN Cui-ping WANG Ming-wei WU Xin-hong MA Biao* 
    2013, 44 (2 ):  224-228.  doi: 10.3969/j.issn.0529-1356.2013.02.015
    Abstract ( )  

    Objective To analyze the difference of aldehyde dehydrogenase 1(ALDH1) and estrogen receptor (ER) expression between primary and corresponding metastatic focuses of breast cancer. Methods A total of 87 female patients diagnosed with metastatic breast cancer were included in this study. Immunohistochemistry (IHC) was used to detect the expression of ALDH1 and ER between primary and metastatic sites. Integrated absorbance (IA) of stained sections was measured by Image-Pro Plus 6.0 (IPP 6.0),and then the statistical analysis was done. Results The incidences of ALDH1 and ER expression among the primary tumor were 28.7%(25 cases) and 56.3% (49 cases), while ascending to 43.7% and declined to 32.2% in corresponding metastatic breast cancer, which were statistically significant respectively (P <0.05 and P <0.01). Statistical analysis results of IA showed that ALDH1 expression in metastatic focuses was obviously higher than that in the corresponding primary tumor, while ER expression was significantly lower. Conclusion The frequencies of ALDH1 positive expression and ER negative expression were more frequently observed in metastatic focuses than in primary breast cancer.

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    Analysis of predictors for No.10 lymph nodes metastasis in advanced gastric cancer
    BU Zhao-de WANG Jian-wei ZHENG Zhi-xue SUN Yu LI Zi-yu ZHANG Wei-guang* JI Jia-fu*
    2013, 44 (2 ):  229-234.  doi: 10.3969/j.issn.0529-1356.2013.02.016
    Abstract ( )  

    Objective To investigate the predictors of No.10 lymph nodes metastasis in patients with the advanced gastric cancer. Methods A retrospective study was performed to analyze 142 patients who underwent D2 curative proximal or total gastrectomy for gastric carcinoma from January 2006 to December 2009. Clinicopathological factors and molecular markers such as sex, age, location of the primary tumor, tumor sizes, gross type, depth of invasion, the metastasis of adjacent lymph node, Ki-67, matrix metalloproteinase(MMP)7, and p53 status were analyzed with univariate and multivariate analysis. Results The overall ratio of metastatic lymph node was 66.2% (94/142). The positive rates of No 10 lymph nodes were 16.2%(23/142). The No 10 lymph node metastasis was correlated with tumor site, size, Borrmann type, depth of invasion, and No4s lymph node metastasis but biomarkers Ki-67, MMP7 and p53. Multivariable logistic regression analysis showed that positive metastasis of No.4s lymph node was an independent risk factor for lymph node metastasis in No.10 lymph nodes. The positive rates of No.10 lymph nodes were 7.8% and 26.6% for the No4s lymph nodes negative patients and positive patients, respectively. Conclusion The status of No4s lymph nodes is an independent risk factor of No.10 lymph nodes metastasis in patients with advanced gastric cancer, but the negative predict value is not low enough to 5 percent. We can’t predict negative No.10 lymph nodes accurately in patients with advanced gastric cancer.

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    Expression survivin and correlation with Caspase-9 and Caspase-3 genes in esophageal cancer of Kazakin in Xinjiang
    LI Xiu-mei CHEN Yan LI Hui PANG Zuo-liang WANG Hong-jiang JIANG Xiao-fang GUO Qiong LI Hui-wu*
    2013, 44 (2 ):  235-237.  doi: 10.3969/j.issn.0529-1356.2013.02.017
    Abstract ( )  

    Objective To investigate the high expressed Survivin and its relationship with the apoptosis proteins in esophageal cancer of Kazakh in Xinjiang. Methods Thirty-four Survivin mRNA differential expression specimens from 52 cases of Kazakh’s esophageal cancer specimen (cancerous tissue expression in quantity than distal normal tissue) were screened. Caspase-9 and Caspase-3 gene and protein expression were detected by RT-PCR and Westernblotting respectively. Results 1. Survivin overexpressed in Kazakh’s esophageal cancer tissue, compared with distal normal tissue, differences were statistically significant (P <0.05); 2. 61.8% of the specimens had Caspase-9 low expression in 34 case specimens with Survivin mRNA differential expression, and the expression of Survivin was negatively correlated to the Caspase-9 expression(r = -0.244,P <0.05); 3. Caspase-9 protein activation significantly decreased(P <0.05). Conclusion The overexpression of Survivin may play an important role in the origin and development of Xinjiang Kazakh’sesophageal cancer. The function of Survivin in regulation of apoptosis may be related to direct inhibition of Caspase-9 and activation of transcription.

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    Changing laws for choke veins of cross-area falp at the dorsum of the rat
    DAI Kai-yu HU Si-wang ZHUANG Yue-hong LIU Yang-wu YANG Jin ZHANG Gen-fu YANG Xiao-dong
    2013, 44 (2 ):  238-244.  doi: 10.3969/j.issn.0529-1356.2013.02.018
    Abstract ( )  

    Objective To investigate the changs of Choke veins for cross-area flap at the dorsum of the rat. Methods Firstly, the vessels distribution of 30 SD rats was studied by lead oxide-gelatin one-time whole vascular perfusion technique. Secondly, a cross-area flap at the size of 10.0cm×3.5cm was cut out at either side of dorsum in 10 SD rats and placed in the skin window. The changes of Choke vessels were observed and photographed for 8 days under the stereomicroscope. The skin windows were placed in another 2 SD rats before 2% Evans blue was injected about 1 ml in each rat by tail vein and the microcirculation of choke vessels was recorded by video. Results After the cross-area flap was cut out, the vascular diameter dilated in both choke artery and veins. However, the most obvious dilation was found in the connection venules. The dilation of connection venules began at the (60±12)th hour after operation and continued till (4.5±0.5) days. The whole circulation process was observed in the Choke vessels by Evans blue injection in tail vein and the blood velocity at the choke artery was approximately 2.53mm/s. Conclusion In the earlier stage following the flap cutting out, the backflow of venous blood gives priority to the labyrinth type, while the backflow of venous blood is valve failure in preference to the labyrinth type at the later stage. Evans blue as a blood tracer is suitable for the blood blow dynamics research in the microcirculation of skin flap when combining with the direct observation of skin window.

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    Anatomy of distal insertion of deep posterior tibiotalar ligament of human ankle
    ZHANG Cheng ZHANG Li-cheng JIANG Wen-hui YANG Guo-jing WANG Wei-liang LIN Guang-mao* LIU Min YANG Xin-dong
    2013, 44 (2 ):  245-248.  doi: 10.3969/j.issn.0529-1356.2013.02.019
    Abstract ( )  

    Objective To provide an anatomic evidence for the suture anchors treatment and reconstruction of deep posterior tibiotalar ligament ,the distal insertions of deep posterior tibiotalar ligament were measured. Methods We studied 30 cadaveric ankles. The insertions of deep posterior tibiotalar ligament were exposed, and their sizes and locations were measured and localized. Results Deep posterior tibiotalar ligament was a constant,and the widest and thickest deltoid ligament. It originated from posterior colliculus and,intercollicular groove of medial ankle, and inserted onto the postermedial talus.The distal insertions were not quadrangular. The areas of distal insertions were(111.74±19.97)mm2. ConclusionThe anatomic characteristic of the distal insertion of the deep posterior tibiotalar ligament was revealed, which provides anatomical basis for surgery.

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    Anatomy and clinical significance of the lower end connection of adult tibia and fibula
    JIANG Wen-hui DONG Yi-long ZHANG Cheng ZHANG Li-cheng* YANG Guo-jing 
    2013, 44 (2 ):  249-252.  doi: 10.3969/j.issn.0529-1356.2013.02.020
    Abstract ( )  

    Objective To investigate the anatomy of the tibiofibular syndesmosis ligaments and to compared the characteristics of the ligament. Methods Thirty adult cadaveric legs were examined in this study. The average age of the cadavers was 61, ranged from 46 to 75 years. Using a layered dissection method, the following data were collected: the average length, width, thickness of anterior tibiofibular ligament, posterior tibiofibular ligament, transverse tibiofibular ligament and intersseous ligament,the angle between anterior tibiofibular ligament, posterior tibiofibular ligament and the horizontal plane,the angle between anterior tibiofibular ligament, posterior tibiofibular ligament and the midpoint of internal and external malleolus. Results The average length of the anterior tibiofibular ligament was (18.18±2.64) mm, width of (13.28±1.82) mm,thickness of (1.98±0.24) mm, and horizontal angle of (38±4) °, the angle with the midpoint of internal and external malleolus was (33±3)°. The average length of the posterior tibiofibular ligament was (16.12±2.40) mm,width of (11.58±1.98) mm,thickness of (2.52±0.32) mm,and horizontal angle of (31±5)°,the angle with the midpoint of internal and external malleolus was 29°±4°. The average length of the transverse tibiofibular ligament was (24.42±4.54) mm,width of (4.96±0.92) mm,thickness of (3.12±0.42) mm;the average length of intersseous ligament was (22.24±3.92) mm,width of (16.42±2.32) mm,thickness of (1.42±0.44) mm. Conclusion This study reveals the anatomical features of the tibiofibular syndesmosis and provides the anatomical basis for clinical application.

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    Association of transcriptional factor GATA4 expression patterns with arterial pole development of embryonic mouse heart
    CAI Yu-jin JING Ya* QIAO Ai-xiu YANG Yan-ping LI Hai-rong CUI Hui-lin ZHANG Tao
    2013, 44 (2 ):  253-258.  doi: 10.3969/j.issn.0529-1356.2013.02.021
    Abstract ( )  

    Objective To explore the relationship of the expression of transcriptional factor GATA4 in the heart-forming field and the foregut endoderm with the morphological development of the arterial pole of embryonic mouse heart.Methods Serial sections of mouse embryos on embryonic day(ED)7.5 to ED13, three embryos from each embryonic day, were stained immunohistochemically or immunofluorescently with antibodies against GATA4, Nkx2.5, insulin gene enhancer binding potein (ISL-1), α-smooth muscle actin and myosin heavy chain. The expression of GATA4 and phosphorylated histone H3(pHH3) were measured with Western blotting in the embryonic mouse hearts from ED11 to ED14. Results At ED7.5, positive cells for both transcription factors GATA4 and Nkx2.5 were found in the cardiogenic plate simultaneously. From ED8.5 to ED10, further expression of GATA4 and Nkx2.5 were detected in the splanchnic mesoderm of the dorsal wall of the pericardial cavity that constituted the second heart field(SHF). From ED11 to ED13, GATA4 and Nkx2.5 expressions were found descending from the reflection of dorsal pericardial wall with the distal pole of outflow tract to the base of the ascending aorta and pulmonary trunk. GATA4 expression was also detected in the foregut endoderm of ED11 to ED13 embryos. GATA4 and pHH3 expression in the embryonic mouse hearts reached the highest level between ED11 and ED13. Conclusion Transcription factor GATA4 shows the same expression pattern as that of Nkx2.5 during the early development of the embryonic mouse heart. Higher expression of GATA4 during crucial stages of heart morphogenesis suggests that GATA4 may play an important role in the proliferation of myocardial cells. The GATA4 expression in the foregut endoderm may be involved in the development of the SHF.

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    Zdhhc17 regulating convergent and extension movements during zebrafish embryogenesis
    YANG Yang GAO Ming CHEN Xue-ran SHI Wei WANG Fen MA Bao-hua HAO Ai-jun*
    2013, 44 (2 ):  259-263.  doi: 10.3969/j.issn.0529-1356.2013.02.022
    Abstract ( )  

    Objective  To investigate the role of zdhhc17 on embryonic development in zebrafish by loss-of-function experiments. Methods Zdhhc17 antisense morpholino oligonucleotide was injected into embryos to block the translation. The whole mount in situ hybridyzation and RT-PCR were used to detect the abnormal development after knockdown of zdhhc17. Results Knockdown of zdhhc17 impacted convergence and extension movements during zebrafish gastrulation. The tail of zdhhc17 morphants was curved and shorter (82/118). The expression patterns of dlx3b, ntl, myod1 and tbx6 were affected. The mRNA level of cdh1 and padh18a was obviously lower in embryos injected with zdhhc17 morpholino. Conclusion zdhhc17 is critical for zebrafish convergence and extension movements via regulating the expression of cadherin superfamily genes cdh1 and pcdh18a and affecting cell adhesion.

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    Effect of  sox19b gene knockdown on the eyes development in zebrafish
    GAO Ming YANG Yang CHEN Xue-ran SHI Wei LIN Yu-shuang, HAO Ai-jun*
    2013, 44 (2 ):  264-268.  doi: 10.3969/j.issn.0529-1356.2013.02.023
    Abstract ( )  

    Objective  To explore the function of sox19b on the eye development in zebrafish by knockdown of sox19b. Methods To inhibit the expression of sox19b by microinjection of sox19b morpholinos(MO)and then observe the effect of the development of the eyes in zebrafish by RT-PCR and the whole-mount in situhybridization. Results The development of the eyes was abnormal after knockdown of sox19b, mainly showed small eyes or eye deficiency and the abnormal retina and lens(n =57/93). The expression of some important genes during the development of the eyes, such as rx3, pax2a and vsx2, was decreased apparently in the sox 19b morphant. Conclusion The transcription factor, sox19b is critical for the development of the eyes via the regulation of the important eye-field transcription factors,EFTEs in early zebrafish embryos.

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    Influence of heroin withdrawal and relapse on the expression of Β-endorphin and adrenocorticotropic hormone in adrenal chromaffin cells and the serum cortisal level in rats
    HUANG Zhi LIANG Wen-mei*
    2013, 44 (2 ):  269-273.  doi: 10.3969/j.issn.0529-1356.2013.02.024
    Abstract ( )  

    Objective  To explore the influence of heroin withdrawal, methadone detoxication and heroin relapse on expression of β-endorphin (β-EP), and adrenocorticotropic hormone( ACTH) in rat adrenal chromaffin cells, and the change of cortisal (COR) level in the serum. Methods Sixty-three adult male SD rats were randomly divided into normal control group(NCG),saline control group (SCG) and experiment groups(EG). The EG groups were further subdivided into heroin withdrawal group (HWG), methadone detoxication group(MDG) and heroin relapse group(HRG). Immunohistochemical SABC method, image analysis and radioimmunoassay technique were used.Results Compared with NCG and SCG,the mean grey value of β-EP-IR cells was increased in HWG. After the treatment of methadone, compared with NCG and SCG,the mean grey value of β-EP cells was lower in MDG.The mean gray value of β-EP cells in HRG was increased but there was no statistical significance when compared with NCG and SCG. Compared with NCG and SCG, the ACTH-IR cells expressed less in the EG groups. Immunohistochemical analysis showed higher grey value in EG rats than that in controls. Serum COR level in the EG groups were at a higher level than that in NCG and SCG (P <0.05). Conclusion Heroin withdrawal, methadone detoxication and heroin relapse have influenced the expression of β-EP and ACTH in adrenal chromaffin cells and the serum COR level in rats.

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    Effects of Ghrelin on the protective effect and influence of growth differentiation factor-15 in the rat with the heart failure induced by myocardial infarction
    TIAN Guo-zhong* WEI Gang LI Mei-xiu ZHONG Zhen-ya ZHU Jin-ling LI Yan-jun YANG Yu WEI Wei 
    2013, 44 (2 ):  274-278.  doi: 10.3969/j.issn.0529-1356.2013.02.025
    Abstract ( )  

    Objective The previous experiment showed that Ghrelin intervened in myocardial infarction leading to heart failure(HF) in rats at the early stage. The aim of this paper is to further investigate the correlation between growth differentiation facto-15 (GDF-15) and HF degree, which might lay a theoretical foundation of HF clinical treatments. Methods Eighty Wistar rats survived 6 hours in the modeling were randomly divided into sham operation(group A)( n =18), HF model (group B)( n =27), HF model of intervention(group C)( n =27). The blood GDF-15 expression level in 3 days,1 week,2 weeks,4 weeks and 8 weeks after surgery and the GDF-15 mRNA expression level in HF myocardial tissue in 2 weeks, 4 weeks and 8 weeks were tested by ELISA and real-time PCR. The rat myocardial ultrastructure was observed by electron microscope. Cardiac function was checked by B ultrasonic before executing the rats. Results Group B blood GDF-15 and myocardial tissue GDF-15 mRNA expression level were significantly higher than group C, but lower than group A. The difference was statistically significant( P <0.001).Ultrasonic testing results showed that group B heart increased significantly,left ventricular systolic and diastolic inner diameter increased obviously than group A and C in the 8 weeks. The difference was statistically significant ( P <0.001). Group B end-diastolic ventricular septal thickness, left ventricular thickness and left ventricular ejection fraction were significantly reduced than group A and C; In addition, myocardial ultrastructure shows group C change significantly than group B. Conclusion Ghrelin early intervention in HF in rats can improve heart function and reduce mortality; GDF-15 expression level can reflect HF lesions degree, and can be a new marker as auxiliary detection of HF.

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     Effects of ultrashort gamete co-incubation time on mouse in vitro fertilization
    JIANG Nan* WANG Yu-jie XU Ying LIU Xia CAI Wen-wei CHANG Yong-fu HUA Ke 
    2013, 44 (2 ):  279-283.  doi: 10.3969/j.issn.0529-1356.2013.02.026
    Abstract ( )  

    Objective To study the impact of gamete co-incubation time on fertilization rate, production of oxidative stress (OS) and embryo quality of mouse in vitro fertilization (IVF), and to investigate the shortest gamete co-incubation time of mouse IVF. Methods Oocytes of ICR mouse were co-incubated with sperm for 30 seconds, 2 minutes, 10 minutes , 0.5 hour, 2 hours, 4 hours and 18 hours, the fertilization rate and the blastocyst rate were analysed in each co-incubation group. In addition, the maleic dialdehyde(MDA) was assessed when gametes were co-incubated for 0 hour, 2 hours and 18 hours. Results Fifty-two, fifty-three, fifty- three, fourty-six, fourty-eight, fourty-eight and fourty-seven oocytes were inseminated with sperm in each group, and the fertilization rate were 67.3%, 81.1%, 83.0%, 87.0%, 85.4%, 81.3% and 48.9% respectively. The fertilization rate of 30 seconds group was significantly lower than 0.5 hour and 2 hours groups( P <0.05). Moreover, the fertilization rate of 18 hours group was significantly lower than 2 minutes, 10min, 0.5 hour, 2 hours and 4 hours groups(P <0.05). No significant differences in fertilization rate were observed in 2 minutes, 10 minutes, 0.5 hour, 2 hours and 4 hours groups(P >0.05). In addition, the blastocyst rate were 82.9%, 65.1%, 70.5%, 67.5%, 75.6%, 71.8% and 65.2%, and no significant differences were observed in each group(P >0.05). The concentrations of MDA were
    (1.06±0.21)×10-3 mol/L, (1.44±0.22)×10-3 mol/L and (2.00±0.21)×10-3 mol/L for 0 hour, 2 hours and 18 hours co-incubation, respectively. As the coincubation time was reduced, the MDA levels were also significantly reduced(P <0.05). Conclusion Reducing the gamete co-incubation time to 2 minutes will not affect the fertilization rate of mouse IVF. As the co-incubation time is reduced, the production of OS is also reduced.

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     Seven behavioral traits of lateral functional dominance of Han nationality in Zhejiang province
    ZHANG Yu-ke LI Yong-lan* LU Shun-hua ZHENG Lian-bin LI Chuan-gang QIAN Hui-ru 
    2013, 44 (2 ):  284-291.  doi: 10.3969/j.issn.0529-1356.2013.02.027
    Abstract ( )  

    Objective To study 7 behavioral traits of lateral functional dominance in zhejiang of Han. Methods Seven behavioral traits of lateral functional dominance ( hand clasping , handedness, arm folding, leg folding, foot preference, stride type and eye preference) on 439 students of Han (195 males and 244 females) in Zhuji city of Zhejiang province were studied. Results The percentages of the right type on 5 traits were much higher than that of left type, except clasping hand and stride type; There was no sexual difference in Zhejiang of Han on 6 traits preference, except folding leg. Comparing with other 8 areas of Han, significant difference were found in the frequencies on 7 behavioral traits of lateral functional dominance between Zhejiang and Guizhou. A small difference was found in Zhejiang and the other Han areas. Comparing with other 13 minority groups, more difference were found in Zhejiang and the other South types of Yi, Miao, Buyi, Dong, Li and a small difference was found in Zhejiang and the other 8 North types. The clasping hand was correlative with folding leg, preferential foot. Handedness was correlative with folding leg, preferential foot, stride type. Folding leg was correlative with preferential foot, stride type. Preferential foot was correlative with stride type, preferential eye. Conclusion The 7 behavioral traits of lateral functional dominance in Zhejiang of han are close to that of Hui and Korean. It is of characteristics of North Asian type.

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    Analysing the muscle development characteristics of Tibetan teenagers in Tibet by using bioelectrical impedance method
    ZHANG Hai-long XI Huan-jiu* FU Qiang LI Wen-hui LIU Su-wei ZHONG Hua BAIMADUOJI
    2013, 44 (2 ):  292-296.  doi: 10.3969/j.issn.0529-1356.2013.02.028
    Abstract ( )  

    Objective Tibetan teenagers in Tibet by counting their muscle mass with bioelectrical impedance method. Methods We selected randomly 1427 healthy teenagers whose parents were Tibetan in Tibet (710 males, 717 females).They had signed the informed consent.We detected all subjects with the body composition analyzer and concluded the total muscle, trunk(left upper limb,right upper limb,left lower limb,right lower limb)muscle mass.All the results were inputted SPSS(statistical software) and processed by independent sample t-test and variance analysis. Results The total muscle mass, trunk(left upper limb,right upper limb,left lower limb,right lower limb)muscle mass of males were all more than those of females in all age groups of Tibetan teenagers( P <0.05 or P <0.01).In general,the muscle mass of Tibetan teenagers in Tibet increased with age,males’ increasing trend was more pronounced. Conclusion The muscle development of Tibetan teenagers in Tibet is related with age and hormone secretion,it reflects the physiological characteristics in different developmental stages.

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