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蹒跚小鼠(tg/tg)中枢神经系统中毒蕈碱型乙酰胆碱受体数量减少。

Decreased muscarinic acetylcholine receptor number in the central nervous system of the tottering (tg/tg) mouse.

作者信息

Liles W C, Taylor S, Finnell R, Lai H, Nathanson N M

出版信息

J Neurochem. 1986 Mar;46(3):977-82. doi: 10.1111/j.1471-4159.1986.tb13065.x.

Abstract

The tottering mouse (tg/tg) is a single-locus mutant, phenotypically characterized by the development of epilepsy associated with distinct electroencephalographic abnormalities. Because of reported alterations in muscarinic receptor (mAChR) number in various seizure states, mAChR density was examined in discrete brain regions of tottering (tg/tg) and coisogenic wild-type (+/+) mice. Saturation binding experiments revealed a widespread decrease in membrane mAChR density in the CNS of adult tottering (tg/tg) mice as compared with age-matched control wild-type (+/+) mice. The decrease was most pronounced in the hippocampus, where tg/tg mice exhibited a 40-60% reduction in mAChR density with no change in the affinity of the receptor for antagonists or agonists. At postnatal day 10, before the reported onset of electroencephalographic abnormalities, 114 and 65% increases in mAChR density were observed in the tg/tg hippocampus and cortex, respectively. Following the development of seizure activity at postnatal day 22, mAChR density in the tg/tg hippocampus was reduced by 29%. No change in brain mAChR density was seen in adult heterozygotes (+/tg), which do not develop electroencephalographic or seizure abnormalities. These results indicate that the development of reduced mAChR number in the CNS of the tg/tg mouse is secondary to abnormal neuronal activity, providing further support for the hypothesis that membrane depolarization can cause a decrease in neuronal mAChR density.

摘要

蹒跚小鼠(tg/tg)是一种单基因座突变体,其表型特征是发展出与明显脑电图异常相关的癫痫。由于报道了各种癫痫状态下毒蕈碱受体(mAChR)数量的改变,因此研究了蹒跚(tg/tg)小鼠和同基因野生型(+/+)小鼠不同脑区的mAChR密度。饱和结合实验显示,与年龄匹配的对照野生型(+/+)小鼠相比,成年蹒跚(tg/tg)小鼠中枢神经系统中膜mAChR密度普遍降低。这种降低在海马体中最为明显,tg/tg小鼠的mAChR密度降低了40%-60%,而受体对拮抗剂或激动剂的亲和力没有变化。在出生后第10天,即在报道的脑电图异常出现之前,tg/tg小鼠的海马体和皮质中mAChR密度分别增加了114%和65%。在出生后第22天癫痫活动发展后,tg/tg小鼠海马体中的mAChR密度降低了29%。成年杂合子(+/tg)没有出现脑电图或癫痫异常,其脑内mAChR密度未见变化。这些结果表明,tg/tg小鼠中枢神经系统中mAChR数量减少是神经元活动异常的继发结果,为膜去极化可导致神经元mAChR密度降低这一假说提供了进一步支持。

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