Goldberg S R
J Pharmacol Exp Ther. 1980 Sep;214(3):726-36.
Squirrel monkeys pressed a key under a two-component, 30-response fixed-ratio schedule of food presentation. In both nonpunishment and punishment components, every 30th key-pressing response resulted in food presentation. In the punishment component, the 11th and 22nd response in each 30-response fixed-ratio also produced a 200msec i.v. injection of 30 to 100 microgram/kg of histamine; this resulted in about an 80% suppression of responding in the punishment component. A second group of squirrel monkeys, with arterial catheters for monitoring of blood pressure and heart rate, received automatic i.v. injections of 30 and 100 microgram/kg of histamine; key presses had no programmed consequences. Mean arterial blood pressure decreased by 5 to 20 min Hg and heart rate increased by 60 to 120 beats/min after each injection of histamine. As an effective punisher, histamine was functionally similar to other noxious stimuli such as electric shock. Behavior suppressed by histamine could be markedly increased by presession i.m. treatment with pentobarbital (3-5.6 mg/kg) or chlordiazepoxide (10-30 mg/kg). Presession i.m. treatment with 1 to 3 mg/kg of the H1-receptor antagonist, diphenhydramine, reversed the punishment effects of histamine but only enhanced the cardiovascular effects of histamine. In contrast, 10 to 30 mg/kg of the H2-receptor antagonist, cimetidine, failed to reverse the punishment effects of histamine but markedly attenuated the cardiovascular effects of histamine. Thus, histamine's suppression of responding appeared to be an H1 effect and did not appear to be related to its effects on blood pressure and heart rate.
松鼠猴在一个两分的、每30次按键呈现一次食物的固定比率食物呈现程序下按键。在非惩罚和惩罚两个部分中,每第30次按键反应都会导致食物呈现。在惩罚部分,每30次按键的固定比率中的第11次和第22次反应还会静脉注射200毫秒、30至100微克/千克的组胺;这导致惩罚部分的反应受到约80%的抑制。第二组松鼠猴带有用于监测血压和心率的动脉导管,接受自动静脉注射30和100微克/千克的组胺;按键没有设定的后果。每次注射组胺后,平均动脉血压下降5至20毫米汞柱,心率增加60至120次/分钟。作为一种有效的惩罚物,组胺在功能上与电击等其他有害刺激相似。组胺抑制的行为可通过注射前肌肉注射戊巴比妥(3 - 5.6毫克/千克)或氯氮卓(10 - 30毫克/千克)而显著增加。注射前肌肉注射1至3毫克/千克的H1受体拮抗剂苯海拉明可逆转组胺的惩罚作用,但仅增强组胺的心血管作用。相比之下,10至30毫克/千克的H2受体拮抗剂西咪替丁未能逆转组胺的惩罚作用,但显著减弱了组胺的心血管作用。因此,组胺对反应的抑制似乎是一种H1效应,且似乎与其对血压和心率的作用无关。