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由DBI(地西泮结合抑制剂)经胰蛋白酶消化产生的一种脑十八烷神经肽,作为苯二氮䓬识别位点的促冲突配体发挥作用。

A brain octadecaneuropeptide generated by tryptic digestion of DBI (diazepam binding inhibitor) functions as a proconflict ligand of benzodiazepine recognition sites.

作者信息

Ferrero P, Guidotti A, Conti-Tronconi B, Costa E

出版信息

Neuropharmacology. 1984 Nov;23(11):1359-62. doi: 10.1016/0028-3908(84)90061-3.

Abstract

An octadecaneuropeptide (ODN) produced by the tryptic digestion of DBI was purified and sequenced and its activity on the Vogel test determined. In vitro ODN displaces 3H-diazepam from specific brain recognition sites and injected intraventricularly in thirsty rats facilitates the onset of behavioral inhibition elicited by punishment. The alpha-amide derivative of ODN is devoid of either action. Evidence is presented suggesting that DBI sequence includes at least two replicas of ODN or one replica of ODN and a fragment with similar if not identical amino acid sequence but identical biological activity.

摘要

通过对DBI进行胰蛋白酶消化产生的一种十八肽(ODN)被纯化、测序,并测定了其在Vogel试验中的活性。在体外,ODN可从特定脑识别位点置换出3H-地西泮,并且向口渴的大鼠脑室内注射时,它会促进由惩罚引发的行为抑制的开始。ODN的α-酰胺衍生物没有这两种作用。有证据表明,DBI序列至少包含ODN的两个重复序列,或者ODN的一个重复序列以及一个氨基酸序列相似(即使不完全相同)但生物活性相同的片段。

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