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有证据表明,基质识别有助于长时程增强(LTP)的稳定,但并非其诱导过程。

Evidence that matrix recognition contributes to stabilization but not induction of LTP.

作者信息

Xiao P, Bahr B A, Staubli U, Vanderklish P W, Lynch G

机构信息

Center for the Neurobiology of Learning and Memory, University of California, Irvine 92717.

出版信息

Neuroreport. 1991 Aug;2(8):461-4. doi: 10.1097/00001756-199108000-00013.

DOI:10.1097/00001756-199108000-00013
PMID:1912480
Abstract

Slices of hippocampus were incubated with Arg-Gly-Asp (RGD) peptides known to block members of the integrin class of matrix receptors. Though the peptides caused no detectable difference in the amount of long-term potentiation (LTP) expressed in the CA1 field 1-2 min after induction with high frequency stimulation, they did produce a reversible, dose dependent decay of LTP over a period of 40 min. This effect was not obtained with various non-RGD control peptides. These results suggest that stabilization of LTP requires adhesive interactions via specific matrix recognition sites, whereas induction and expression do not.

摘要

将海马体切片与已知可阻断整合素类基质受体成员的精氨酸-甘氨酸-天冬氨酸(RGD)肽一起孵育。尽管在用高频刺激诱导后1-2分钟,这些肽在CA1区表达的长时程增强(LTP)量上没有引起可检测到的差异,但它们确实在40分钟的时间内产生了LTP的可逆的、剂量依赖性衰减。用各种非RGD对照肽未获得这种效果。这些结果表明,LTP的稳定需要通过特定的基质识别位点进行粘附相互作用,而诱导和表达则不需要。

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