Chojnacka-Wójcik E
Institute of Pharmacology, Polish Academy of Sciences, Kraków.
Pol J Pharmacol Pharm. 1992 May-Jun;44(3):251-60.
To investigate a possible functional interaction between 5-HT1B and 5-HT1A or 5-HT2 receptors we studied the effects of 5-HT1A selective agonists 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) and gepirone, of a 5-HT1A/5-HT2 agonist 5-methoxy-N,N-dimethyltryptamine (5-MeODMT) and of a putative 5-HT2 agonist (+/-)1-(2,5-dimethoxy-4-iodophenyl)-2-amino-propane (+/- DOI) on the 5-HT1B receptor-mediated hypothermia induced by m-trifluoromethylphenylpiperazine (TFMPP) (25 mg/kg) or m-chlorophenylpiperazine (m-CPP) (20 mg/kg) in mice. 8-OH-DPAT (1.25-5 mg/kg), gepirone (1.25-5 mg/kg), 5-MeODMT (2-8 mg/kg) and (+/-)DOI (0.5-2 mg/kg) reduced dose-dependently the TFMPP- or m-CPP-induced hypothermia. At the same time 8-OH-DPAT (2.5 and 5 mg/kg, but not 1.25 mg/kg) and gepirone (1.25-5 mg/kg) themselves decreased the body temperature in mice, while 5-MeODMT (2-8 mg/kg) and (+/-)DOI (0.5-2 mg/kg) did not affect it. The present results suggest that a functional interaction exists between 5-HT1B and 5-HT1A or 5-HT2 receptors.
为了研究5-HT1B与5-HT1A或5-HT2受体之间可能存在的功能相互作用,我们研究了5-HT1A选择性激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)和吉哌隆、5-HT1A/5-HT2激动剂5-甲氧基-N,N-二甲基色胺(5-MeODMT)以及一种假定的5-HT2激动剂(±)1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(± DOI)对间三氟甲基苯基哌嗪(TFMPP)(25 mg/kg)或间氯苯基哌嗪(m-CPP)(20 mg/kg)诱导的小鼠5-HT1B受体介导的体温过低的影响。8-OH-DPAT(1.25 - 5 mg/kg)、吉哌隆(1.25 - 5 mg/kg)、5-MeODMT(2 - 8 mg/kg)和(±)DOI(0.5 - 2 mg/kg)剂量依赖性地降低了TFMPP或m-CPP诱导的体温过低。同时,8-OH-DPAT(2.5和5 mg/kg,但1.25 mg/kg无效)和吉哌隆(1.25 - 5 mg/kg)本身可降低小鼠体温,而5-MeODMT(2 - 8 mg/kg)和(±)DOI(0.5 - 2 mg/kg)对其无影响。目前的结果表明5-HT1B与5-HT1A或5-HT2受体之间存在功能相互作用。