MacKenzie-Taylor D R, Rech R H
Department of Pharmacology and Toxicology, Michigan State University, East Lansing 48824.
Pharmacol Biochem Behav. 1991 Jun;39(2):249-56. doi: 10.1016/0091-3057(91)90175-2.
The development of behavioral tolerance to pentobarbital-induced hypothermia, as separable from cellular and metabolic tolerance, was established. Pentobarbital (PB) was administered to 4 groups of rats, 2 groups of which received intermittent (INT) IP PB treatment. One of these groups, INT/EXP, experienced the hypothermic (measured as rectal body temperature) drug effect after PB injection. The other group, INT/NONEXP, was monitored for body temperature functions (room temperature) before receiving PB (vehicle administration) and then prevented from experiencing PB-induced hypothermia by maintenance of body temperature with a towel wrap restraint and a heating lamp. The INT/EXP group also received equivalent exposure to this towel wrap after vehicle administration. Two other groups received chronic PB treatment (IP and in ground chow), one with experience for hypothermia after injections (CHR/EXP) and one prevented from experiencing the hypothermia (CHR/NONEXP). These groups also received equivalent exposure to the body temperature (at room temperature) testing and towel wrap restraint, EXP rats after vehicle injections and NONEXP after drug injections. A postchronic test of all groups compared the extent of PB hypothermia to prechronic test effects to assess the degree of tolerance. The INT/EXP group demonstrated behavioral tolerance for PB-induced hypothermia, as contrasted with the INT/NONEXP group which demonstrated little or no tolerance. Prominent tolerance was noted in both chronic groups for PB hypothermia, without a significant difference between them. After the postchronic test, chronic treatment was discontinued for 9 days (withdrawal) followed by 9 days of extinction training (vehicle behavioral testing). The two intermittent groups demonstrated no change in the hypothermic drug response during the postwithdrawal and postextinction drug tests.(ABSTRACT TRUNCATED AT 250 WORDS)
已证实对戊巴比妥诱导的体温过低产生行为耐受性,这与细胞和代谢耐受性是可分离的。将戊巴比妥(PB)给予4组大鼠,其中2组接受间歇性(INT)腹腔注射PB治疗。其中一组,INT/EXP,在注射PB后经历低温(以直肠体温测量)药物效应。另一组,INT/NONEXP,在接受PB(赋形剂给药)之前监测体温功能(室温),然后通过用毛巾包裹约束和加热灯维持体温来防止经历PB诱导的体温过低。INT/EXP组在赋形剂给药后也接受了等效的毛巾包裹暴露。另外两组接受慢性PB治疗(腹腔注射和混入食物中),一组在注射后经历低温(CHR/EXP),一组防止经历低温(CHR/NONEXP)。这些组在体温(室温)测试和毛巾包裹约束方面也接受了等效暴露,EXP大鼠在赋形剂注射后,NONEXP大鼠在药物注射后。对所有组进行慢性给药后测试,将PB低温的程度与慢性给药前测试效果进行比较,以评估耐受程度。INT/EXP组表现出对PB诱导的体温过低的行为耐受性,与之形成对比的是,INT/NONEXP组表现出很少或没有耐受性。在两个慢性组中均观察到对PB低温的显著耐受性,它们之间无显著差异。慢性给药后测试后,停止慢性治疗9天(撤药),随后进行9天的消退训练(赋形剂行为测试)。在撤药后和消退后药物测试期间,两个间歇性组的低温药物反应没有变化。(摘要截短至250字)