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纳洛酮对血管性痴呆大鼠海马神经细胞形态和超微结构的影响 被引量:2

Effects of Naloxone on the Morphology and Structure of Hippocampal CAl Pyramidal Neurons of Rats with Vascular Dementia
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摘要 目的研究纳洛酮对血管性痴呆(vascu lar dem entia,VD)大鼠海马神经细胞形态和超微结构的影响。方法采用双侧颈总动脉永久结扎方法制备VD大鼠。随机分为3组:假手术组,VD组,VD纳洛酮治疗组(每天0.8 mg/kg纳洛酮腹腔注射,连续7 d)。采用N issl染色观察海马神经细胞形态和数量,电子显微镜观察海马神经细胞超微结构。结果VD大鼠CA1区锥体细胞数(66.21±19.34)和纳洛酮组的(101.68±20.06)与假手术组的(157.11±12.27)相比,分别显著减少,差异有统计学意义(P<0.01),其中纳洛酮组大鼠的细胞数比VD组明显增多(P<0.01)。纳洛酮组大鼠海马CA1区锥体细胞超微结构较VD组明显改善。结论纳洛酮可以减少VD大鼠海马神经细胞的丢失并改善神经细胞的超微结构。 [ Objective] To investigate the effect of naloxone ( NAL) on the morphology and structural changes of pyramidal neurons in hippocampal CA1 of rats with vascular dementia ( VD ). [ Methods ] Vascular dementia was established by permanent occlusion of the common carotid arteries. Rates were divided into three groups: sham - operation group, VD group and VD - naloxone group ( naloxone 0.8 mg/kg, ip daily for 7 days ). Nissl staining and electron microscope were used to observe the morphology and structure of pyramidal neurons in hipocampal CA1 of rats with vascular dementia. [ Results ] CA1 pyramidal neuron counting in the VD group ( 66.21 ± 19.34 ) was significantly lower than that in the naloxone group ( 101,68 ± 20.06 ) and the sham - operation group ( 157.11 ± 12.2 ) , the difference was significant ( P 〈 0.01) ; the neuron counting in the naloxone group was obviously higher than that in the VD group ( P 〈 0.01). CAI pyramidal neurons ultramicro structure in the naloxone group was obviously improved com- pared with the VD group. [ Conclusion] Naloxone could inhibit the loss of hippoeampal CA1 pyramidal neurons in rats with VD and improve the ultramicro structure of neurons.
出处 《职业与健康》 CAS 2006年第21期1780-1783,共4页 Occupation and Health
基金 广东省自然科学基金项目(000825)
关键词 血管性痴呆 纳洛酮 神经细胞 海马 Vascular dementia Naloxone Neurons Hippocampal
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  • 1Sun Shi - lei, Xu Xiao - hu, Ma Guang - yu, et al. Effect of NAL on cognitive function in vascular dementia in rats. Indian J Med Rest,2002, 115:265 -269.
  • 2Ni J, Ohta H, Matsumoto K, et al. Progressive cognitive impairment following chronic cerebral hypoperfusion induced by permanent occlusion of bilateral carotid arteries in rats. Brain Res, 1994, 653:231 -236.
  • 3Cleary J, Semotuk M, Levine AS. Effects of neuropeptide Y on short -term memory. Brain Res, 1994,653:210 -214.
  • 4Sollertinskaya TN. Comparative study of the roles of ACTH and beha - endophin in regulation conditioned reflex activity in the hedgehog. Neurosci Behav Physiol, 1997,27:663 - 671.
  • 5Squire LR. Memory and hippocampus: a synthesis from findings with rats, monkeys, and humans. Psychol Rev, 1992,99 : 195 - 231.
  • 6Olsen GM, Shecl Kuger J, Moiler A, et al. Relation of spatial learning of rats in the Morris water maze task to the number of visible CA1 neurons following four - vessel occlusion. Behav Neurosci, 1994,108 : 681- 690.
  • 7Akhondzadeh S. Hippocampal synaptic plasticity and cognition. J Clin Pharmacol Ther, 1999,24:241 - 248.
  • 8Zarow C, Vinters HV, Ellis WG, et al. Correlates of hippocampal neuron number in Alzheimerg disease and ischemic vascular dementia. Ann Neurol, 2005,57:896-903.
  • 9Zola Morgan S, Squire LR, Amaral DG. Human amnesia and medial temporal regulation: Enduring memory impairment following bilateral lesion limited to field CA1 of the hippocampus. Neurosci, 1986,6:2950 -2967.
  • 10Vertes Z, Melegh G, Vertes M, et al. Effect of naloxone and D - Met - Pro - enkephalinamide treatment on the synthesis in the developing rat brain. Life Sci, 1982,31:119 -126.

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