Lebrun C J, Gruber M G, Meister M, Unger T
Department of Pharmacology, University of Heidelberg, F.R.G.
Brain Res. 1990 Oct 29;531(1-2):167-72. doi: 10.1016/0006-8993(90)90770-c.
Previous in vivo and in vitro studies have demonstrated that exposure of the brain to arginine vasopressin (AVP) can potentiate various responses to a second central challenge with AVP. To determine whether this sensitization is mediated by changes at the receptor level, we investigated the effects of AVP on the phosphoinositide metabolism in septal slices prepared from rats centrally pretreated with saline or AVP. Addition of vasopressin (10(-7) M, 10(-6) M) to septal slices from saline-pretreated rats failed to elicit a significant stimulation of inositol-1-phosphate (IP1). In contrast, AVP (10(-7) M) significantly stimulated IP1 release in septal slices prepared from rats pretreated intracerebroventricularly (i.c.v.) 24 h earlier with 10 or 100 ng AVP. Pretreatment with the same i.c.v. doses of AVP also induced a significant enhancement of the carbachol-induced stimulation of IP1 release, but i.e.v. pretreatment with carbachol did not stimulate the IP1 release in response to AVP. Our results suggest that a novel facilitation of phosphoinositide metabolism can be induced by central AVP pretreatment.
先前的体内和体外研究表明,将大脑暴露于精氨酸加压素(AVP)下,可增强对第二次AVP中枢刺激的各种反应。为了确定这种致敏作用是否由受体水平的变化介导,我们研究了AVP对用生理盐水或AVP进行中枢预处理的大鼠制备的隔区切片中磷酸肌醇代谢的影响。向用生理盐水预处理的大鼠的隔区切片中添加加压素(10^(-7)M,10^(-6)M)未能引起肌醇-1-磷酸(IP1)的显著刺激。相比之下,AVP(10^(-7)M)显著刺激了24小时前经脑室内(i.c.v.)注射10或100 ng AVP预处理的大鼠制备的隔区切片中IP1的释放。用相同i.c.v.剂量的AVP预处理也显著增强了卡巴胆碱诱导的IP1释放刺激,但用卡巴胆碱进行i.c.v.预处理并未刺激对AVP的IP1释放。我们的结果表明,中枢AVP预处理可诱导磷酸肌醇代谢的一种新的促进作用。