Koob G F, Lebrun C, Martinez J L, Dantzer R, Le Moal M, Bloom F E
Ann N Y Acad Sci. 1985;444:194-202. doi: 10.1111/j.1749-6632.1985.tb37589.x.
Arginine vasopressin (AVP) has been shown to have several non-renal actions including the potentiation of learned avoidance behavior in rats and improvement in cognitive functioning in humans. Research in our laboratory has confirmed these behavioral effects in rats using both peripheral and central injection of AVP. We have begun to examine the physiological basis for these effects. Peripheral administration of a vasopressor AVP antagonist reversed the prolongation of extinction produced by peripherally administered AVP in both active and passive avoidance, but also reversed the aversive unconditioned effects of AVP. However, central administration of the vasopressor AVP antagonist reversed peripheral effects of AVP only at doses shown to act peripherally to reverse vasopressor effects of AVP. An osmotic stress in doses known to liberate endogenous AVP mimicked the behavioral effects of exogenously administered AVP, and this stress effect was reversed by the AVP antagonist. These results support our hypothesis of separate but parallel AVP systems in the pituitary and brain with a role in behavioral adaptation to certain types of stress.
精氨酸加压素(AVP)已被证明具有多种非肾脏作用,包括增强大鼠的习得性回避行为以及改善人类的认知功能。我们实验室的研究已通过外周和中枢注射AVP证实了其在大鼠中的这些行为效应。我们已开始研究这些效应的生理基础。外周给予血管加压素AVP拮抗剂可逆转外周给予AVP在主动和被动回避中所产生的消退延长,但也会逆转AVP的厌恶非条件效应。然而,中枢给予血管加压素AVP拮抗剂仅在显示可在外周发挥作用以逆转AVP血管加压效应的剂量下,才会逆转AVP的外周效应。已知能释放内源性AVP的剂量的渗透应激模拟了外源性给予AVP的行为效应,并且这种应激效应可被AVP拮抗剂逆转。这些结果支持了我们关于垂体和大脑中独立但平行的AVP系统在行为适应某些类型应激中起作用的假设。