Kelleher D L, Fregly M J
Department of Physiology, University of Florida, College of Medicine, Gainesville.
Pharmacology. 1987;35(4):203-16. doi: 10.1159/000138312.
Earlier studies have shown that chronic treatment with estradiol benzoate reduced the responsiveness of heart rate, drinking, and tail-skin temperature to administration of the beta-adrenergic agonist, isoproterenol. The objective of the present study was to assess the relationship between the isoproterenol-induced elevations in rate of oxygen consumption and tail-skin temperature in adult ovariectomized rats treated chronically with estradiol benzoate (28 micrograms/day) and untreated, ovariectomized controls. Isoproterenol (0, 10, 25, and 50 micrograms/kg, s.c.) elevated both rate of oxygen consumption and tail-skin temperature in ovariectomized and ovariectomized plus estradiol benzoate-treated rats in a dose-related fashion. However, in both cases the response of the estradiol-treated group was less than that of controls. A comparison of the regressions of rate of oxygen consumption versus dose of isoproterenol administered to each group revealed significant differences between the intercepts, but not the slopes. A similar comparison with respect to the regression of tail-skin temperature versus dose of isoproterenol administered to each group revealed significant differences between both the slopes and intercepts of the relationships. A comparison of the regressions of rate of oxygen consumption versus tail-skin temperature for control and estrogen-treated rats revealed significant differences between both slopes and intercepts of the relationships. The latter comparison suggests a reduced change in tail-skin temperature for a given change in rate of oxygen consumption in the estrogen-treated group. It is concluded from these results that the reduction in metabolic response to beta-adrenergic stimulation in estrogen-treated rats explains, in part at least, the attenuated response of tail-skin temperature. The tail of the rat is important in short-term temperature regulation. When threatened acutely with overheating, the rat uses its tail as a heat radiator, increasing its skin blood flow, temperature, and heat loss. Administration of isoproterenol to rats at doses of 50-100 micrograms/kg, subcutaneously can increase tail-skin temperature as much as 6 degrees C. This response is mediated by beta-adrenoceptors since it can be either attenuated or prevented by prior administration of propranolol. It serves as a simple and reliable test of beta-adrenergic responsiveness in rats. Chronic treatment with the oral contraceptive, Enovid (7.5 mg/kg food) attenuated this response. Chronic administration of the estrogenic component (ethinyl estradiol, 48-50 micrograms/kg/day) of Enovid also attenuated the response.(ABSTRACT TRUNCATED AT 400 WORDS)
早期研究表明,用苯甲酸雌二醇进行长期治疗会降低心率、饮水量以及尾皮温度对β-肾上腺素能激动剂异丙肾上腺素给药的反应性。本研究的目的是评估在长期接受苯甲酸雌二醇(28微克/天)治疗的成年去卵巢大鼠和未治疗的去卵巢对照大鼠中,异丙肾上腺素诱导的耗氧率升高与尾皮温度之间的关系。异丙肾上腺素(0、10、25和50微克/千克,皮下注射)以剂量相关的方式提高了去卵巢大鼠以及去卵巢加苯甲酸雌二醇治疗大鼠的耗氧率和尾皮温度。然而,在这两种情况下,雌二醇治疗组的反应均小于对照组。对每组给予异丙肾上腺素剂量与耗氧率的回归分析比较显示,截距之间存在显著差异,但斜率无显著差异。对每组给予异丙肾上腺素剂量与尾皮温度的回归进行类似比较显示,两者关系的斜率和截距均存在显著差异。对对照大鼠和雌激素治疗大鼠的耗氧率与尾皮温度的回归分析比较显示,两者关系的斜率和截距均存在显著差异。后一项比较表明,在雌激素治疗组中,对于给定的耗氧率变化,尾皮温度的变化减小。从这些结果可以得出结论,雌激素治疗大鼠中对β-肾上腺素能刺激的代谢反应降低至少部分解释了尾皮温度反应减弱的原因。大鼠的尾巴在短期体温调节中很重要。当受到急性过热威胁时,大鼠会将尾巴用作散热器,增加皮肤血流量、温度和热量散失。以50 - 100微克/千克的剂量皮下给大鼠注射异丙肾上腺素可使尾皮温度升高多达6摄氏度。这种反应由β-肾上腺素能受体介导,因为预先给予普萘洛尔可使其减弱或阻止。它是大鼠β-肾上腺素能反应性的一种简单可靠的测试。用口服避孕药炔雌醇甲醚(7.5毫克/千克食物)进行长期治疗会减弱这种反应。长期给予炔雌醇甲醚的雌激素成分(炔雌醇,48 - 50微克/千克/天)也会减弱这种反应。(摘要截于400字)