Järvinen A, Paakkari I
Department of Pharmacology and Toxicology, University of Helsinki, Finland.
Pharmacol Toxicol. 1991 Apr;68(4):270-5. doi: 10.1111/j.1600-0773.1991.tb01237.x.
The development of tachyphylaxis to the pressor, tachycardiac, ventilatory and smooth muscle effects of thyrotropin-releasing hormone (TRH) was studied. Subsequent administrations of increasing doses of TRH (0.1-1000 nmol/kg intracerebroventricularly), at 20 min. intervals in urethane-anesthetized rats dose-dependently increased the mean arterial blood pressure, heart rate and minute ventilation volume. At all doses the effect on mean arterial blood pressure was apparent at least 20 min. after each injection whereas at low doses (0.1-1 nmol/kg) the duration of the effects on heart rate or minute ventilation volume were shorter. The cardiorespiratory effects of TRH 10 nmol/kg intracerebroventricularly did not subside completely within an observation period of 1 hr. However, a repeated administration of TRH at 1 hr resulted in the levels of mean arterial blood pressure, heart rate and minute ventilation volume not statistically different from the peak levels of the first injection. While the cardiorespiratory effects of TRH were long-lasting, the TRH induced inhibition of the contractions of the rat duodenal smooth muscle lasted only 12-18 sec. The TRH-treated duodenal preparation responded normally to noradrenaline but remained unresponsive to further administrations of TRH until washed extensively. When the medium after cessation of the TRH response was transferred into another chamber with an untreated preparation, a full response was resulted. Inhibitors of TRH metabolism, bacitracin, EDTA and iodoacetamide, did not prolong nor enhance the response. Likewise, a stable TRH-analogue MK-771 did not produce any longer response than TRH. It is concluded that no tachyphylaxis was produced to the neurally mediated pressor, tachycardiac or ventilatory effects of TRH.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了对促甲状腺激素释放激素(TRH)的升压、心动过速、通气及平滑肌效应快速耐受性的发展。在氨基甲酸乙酯麻醉的大鼠中,每隔20分钟脑室内注射递增剂量的TRH(0.1 - 1000 nmol/kg),剂量依赖性地增加平均动脉血压、心率和每分钟通气量。在所有剂量下,每次注射后至少20分钟对平均动脉血压的影响明显,而在低剂量(0.1 - 1 nmol/kg)时,对心率或每分钟通气量的影响持续时间较短。脑室内注射10 nmol/kg的TRH对心肺的效应在1小时的观察期内未完全消退。然而,1小时后重复注射TRH导致平均动脉血压、心率和每分钟通气量水平与首次注射的峰值水平无统计学差异。虽然TRH对心肺的效应持久,但TRH诱导的大鼠十二指肠平滑肌收缩抑制仅持续12 - 18秒。经TRH处理的十二指肠制剂对去甲肾上腺素反应正常,但在广泛冲洗前对进一步注射的TRH无反应。当TRH反应停止后的培养基转移到另一个未处理制剂的腔室中时,产生了完全反应。TRH代谢抑制剂杆菌肽、乙二胺四乙酸和碘乙酰胺并未延长或增强反应。同样,稳定的TRH类似物MK - 771产生的反应并不比TRH更长。结论是,对TRH的神经介导的升压、心动过速或通气效应未产生快速耐受性。(摘要截短于250字)