Zamfir O, Broqua P, Baudrie V, Chaouloff F
Laboratoire de Pharmacologie, CNRS, CHU Necker, Paris, France.
Eur J Pharmacol. 1992 Aug 25;219(2):261-9. doi: 10.1016/0014-2999(92)90304-m.
The purpose of the present study was to analyze the influence of stress (24-h cold exposure) on presynaptic 5-HT1A receptors, and on postsynaptic 5-HT1A, 5-HT1C and 5-HT2 receptors. Cold exposure for 24 h affected neither pargyline-induced decreases in 5-hydroxyindoleacetic acid (5-HIAA) levels in midbrain and rest of brain, nor plasma glucose and corticosterone levels. Treatment with the 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; 0.5-1 mg/kg), 3-5 h after the end of cold exposure triggered less intense flat body posture and forepaw treading in cold-exposed rats than in controls. On the other hand, 15- and 30-min plasma glucose responses to 8-OH-DPAT (0.25-0.5 mg/kg, 3-5 h after cold) or to the alpha 2-adrenoceptor agonist, clonidine (0.025 mg/kg), were not affected by cold, while the 15-min, but not the 30 min, plasma corticosterone response to 8-OH-DPAT was slightly amplified in cold-exposed rats. Cold exposure affected neither the inhibitory effect of 8-OH-DPAT (0.25-0.5 mg/kg, 3-5 h after cold) on midbrain 5-HIAA levels, nor the hypothermic effect of 8-OH-DPAT (0.5-1 mg/kg, 3-5 h after cold). Lastly, the hypoactivity elicited by the 5-HT1C receptor agonist, m-chlorophenyl-piperazine (1.5-3 mg/kg, 3-5 h after cold), or head shakes elicited by the 5-HT2 receptor agonist, 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (1-2 mg/kg, 3-5 h after cold), were of similar intensities in control and in cold-exposed rats.
本研究的目的是分析应激(24小时冷暴露)对突触前5-羟色胺1A(5-HT1A)受体以及突触后5-HT1A、5-HT1C和5-HT2受体的影响。24小时的冷暴露既未影响帕吉林诱导的中脑及脑其他部位5-羟吲哚乙酸(5-HIAA)水平的降低,也未影响血浆葡萄糖和皮质酮水平。在冷暴露结束后3至5小时,用5-HT1A受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT;0.5 - 1毫克/千克)进行处理时,与对照组相比,冷暴露大鼠出现的身体平伏姿势和前爪踏地现象没那么强烈。另一方面,冷暴露对8-OH-DPAT(0.25 - 0.5毫克/千克,冷暴露后3 - 5小时)或α2 - 肾上腺素能受体激动剂可乐定(0.025毫克/千克)引起的15分钟和30分钟血浆葡萄糖反应没有影响,而冷暴露大鼠对8-OH-DPAT的15分钟血浆皮质酮反应(而非30分钟反应)略有增强。冷暴露既未影响8-OH-DPAT(0.25 - 0.5毫克/千克,冷暴露后3 - 5小时)对中脑5-HIAA水平的抑制作用,也未影响8-OH-DPAT(0.5 - 1毫克/千克,冷暴露后3 - 5小时)的降温作用。最后,5-HT1C受体激动剂间氯苯哌嗪(1.5 - 3毫克/千克,冷暴露后3 - 5小时)引起的活动减少或5-HT2受体激动剂1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(1 - 2毫克/千克,冷暴露后3 - 5小时)引起的摇头现象,在对照组和冷暴露大鼠中强度相似。