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大鼠骨骼肌挫伤后p-CB1R的表达及与损伤时间的相关性 被引量:2

The time-dependent expression of p-CB1R during repair of skeletal muscle contusion in rats
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摘要 目的观察探讨大鼠骨骼肌挫伤愈合过程中p-CB1R的表达规律与损伤时间的相关性。方法健康成年雄性SD大鼠50只,体重220~250g,随机分为10组,每组5只,其中9组为实验组,1组为正常对照组。应用免疫组织化学染色和Western blot技术,检测50例大鼠骨骼肌挫伤后各时间段p-CB1R的表达情况。结果正常对照组大鼠骨骼肌未见p-CB1R表达;挫伤后p-CB1R阳性表达主要在单核细胞和成纤维细胞中,各时间段大鼠骨骼肌均未见阳性反应。伤后3~24h,阳性细胞以单核细胞为主;3~5d,阳性细胞以单核细胞和成纤维细胞为主;7~10d,阳性反应主要见于成纤维细胞,并于7d达到高峰;14d,p-CB1R阳性表达量有所下降。结论骨骼肌挫伤愈合过程中p-CB1R在单核细胞和成纤维细胞中的变化具有时序性,可望作为法医学推断骨骼肌挫伤时间的参考指标之一。 Objective To investigate the expression of p-CB1R during wound healing of skeletal muscle contusion in rats and to explore the applicability of p-CB1R to wound age estimation.Methods A total of 50 male,healthy rats,weighting 220~250g were divided into 10 groups randomly.The changes of p-CB1R expression were assessed by immunostaining and Western blotting.Results The expression of p-CB1R was neither detected in skeletal muscle fibers in control rats nor wounded skeletal muscle.No-immunoreactivity of p-CB1R was detected in polymorphonuclear cells(PMNs) in the wound specimens.p-CB1R-positive immunostaining was detected in mononuclear cells(MNCs) in the wounded specimens aged from 3h to 1d.From 3d to 5d postwounding,p-CB1R-immunoreactivity was mainly found in MNCs and fibroblastic cells(FBCs),and mainly in FBCs from 7d to 10d postwounding with a peak at the 7d and then decreased at 14d.A similar tendency for p-CB1R protein changes was noted as determined by Western blotting.Conclusion p-CB1R is time-dependently expressed in MNCs and FBCs during wound healing of skeletal muscle contusion in rats,suggesting that it may be used as a marker for wound age determination.
出处 《中国法医学杂志》 CSCD 北大核心 2010年第5期308-311,共4页 Chinese Journal of Forensic Medicine
基金 教育部高等学校博士学科点专项科研基金(200801590020)
关键词 法医病理学 骨骼肌挫伤 p-CB1R 损伤时间推断 forensic pathology skeletal muscle contusion p-CB1R wound age determination
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参考文献7

  • 1Matsuda L A,Lolait S J,Brownstein M J,et al.Structure of a cannabinoid receptor and functional expression of the cloned cDNA[J].Nature,1990,346(6284): 561-564.
  • 2Teixeira-Clerc F,Julien B,Grenard P,et al.CB1 cannabinoid receptor antagonism: a new strategy for the treatment of liver fibrosis[J].Nature Medicine,2006,12(6): 671-676.
  • 3于天水,官大威,程子惠,赵锐,胡更奕,朱瑞霞,王玲,郭晓冲,王昌亮.大鼠骨骼肌钝挫伤分级模型的建立[J].法医学杂志,2008,24(3):168-171. 被引量:10
  • 4Hayashi S,Aso H,Watanabe K,et al.Sequence of IGF-I,IGF-II,and HGF expression in regenerating skeletal muscle[J].Histochem Cell Biol,2004,122(5): 427-434.
  • 5Ros J,Claria J,To-Figueras J,et al.Endogenous cannabinoids a new system involved in the homeostasis of arterial pressure in experimental cirrhosis in the rat[J].Gastroenterology,2002,122(1):85-93.
  • 6Eckardt K,Sell H,Taube A,et al.Cannabinoid type 1 receptors in human skeletal muscle cells participate in the negative crosstalk between fat and muscle[J].Diabetologia,2009,52: 664-674.
  • 7Vaidya V S,Shankar K,Locke E,et al.Molecular mechanisms of renal tissue repair in survival from acute renal tubule necrosis:role of ERK1/2 pathway[J].Toxicol PathoL,2003,31(6): 604-618.

二级参考文献7

  • 1吴旭,王保捷,张国华,官大威,汪德文,杨丽,刘长胜.大鼠脑损伤分级自由落体打击模型的建立[J].中国法医学杂志,2005,20(1):1-3. 被引量:35
  • 2官大威,徐建青,李德祥,李庆生,金鑫,王怀良,贾静涛.实验性心脏挫伤动物模型的建立[J].中国法医学杂志,1995,10(2):65-67. 被引量:5
  • 3Hurme T, Kalimo H. Activation of myogenic precursor cells after muscle injury [J]. Med Sci Sports Exerc, 1992, 24(2): 197-205.
  • 4Allbrook D, Baker WC, Kinkaldy-Willis WH. Muscle regeneration in experimental animnals and in man. The cycle of tissue change that follows trauma in the injured limb syndrome[J]. J Bone Joint Surg Br, 1966,8(1): 153- 169.
  • 5Gutmann E, Carlson BM. The regeneration of a hormonesensitive muscle (levator ani)in the rat [J]. Exp Neurol, 1978, 58(3): 535-548.
  • 6Kami K, Masuhara M, Kashiba H, et al. Changes of vinculin and extracellular matrix components following blunt trauma to rat skeletal muscle[J]. Med Sci Sports Exerc, 1993, 25(7): 832-840
  • 7Lighthall JW. Controlled cortical impact: a new experimental brain injury Model[J] . J Neurotrauma, 1988, 5(1): 1-15.

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