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α1肾上腺素能受体激动剂SDZ NVI-085在豚鼠中产生5-HT1D受体介导的低温效应的证据。

Evidence for a 5-HT1D receptor-mediated hypothermic effect of the alpha 1-adrenoceptor agonist, SDZ NVI-085, in guinea-pigs.

作者信息

Kalkman H O, Neumann V

机构信息

Preclinical Research, Sandoz Pharma Ltd., Basel, Switzerland.

出版信息

Eur J Pharmacol. 1995 Oct 24;285(3):313-5. doi: 10.1016/0014-2999(95)00526-q.

Abstract

The alpha 1-adrenoceptor agonist, SDZ NVI-085 ((-)-(4aR,10aR)-3,4,4a,5,10,10a-hexahydro-6-methoxy-4- methyl-9-(methylthio)-2H-naphth[2,3-b]-1,4-oxazine.HCl; 1 mg/kg i.p.), decreased body temperature of guinea-pigs. Two 5-HT1D receptor antagonists, GR127935 (N-[4-methoxy-3-(4-methyl-1-piperazinyl)phenyl]-2'-methyl-4'-(5-methyl- 1,2,4-oxadiazol-3yl)[1,1-biphenyl]-4-carboxamide) and PAPP (p-aminophenylethyl-m-trifluoromethylphenyl piperazine; both compounds at 1 mg/kg i.p., -30 min) blocked this response, whilst the alpha 1-adrenoceptor blocker prazosin (1 mg/kg i.p.) and the 5-HT1A receptor antagonist, SDZ 216-525 (methyl 4-(-[4-(1,1m3-trioxo-2H-1,2-benzoisothiazol-2-yl)butyl ]-1-piperazinyl)1H- indole-2-carboxylate; 1 mg/kg i.p.) were inactive. Another alpha 1-adrenoceptor agonist, St 587 (2-(2-chloro-5-trifluoromethylphenylimino)-imidazoline; 1 mg/kg i.p.) did not alter body temperature. SDZ NVI-085-induced hypothermia in guinea-pigs is probably mediated by 5-HT1D receptors.

摘要

α1肾上腺素能受体激动剂SDZ NVI-085((-)-(4aR,10aR)-3,4,4a,5,10,10a-六氢-6-甲氧基-4-甲基-9-(甲硫基)-2H-萘并[2,3-b]-1,4-恶嗪·盐酸盐;腹腔注射1mg/kg)可降低豚鼠体温。两种5-HT1D受体拮抗剂GR127935(N-[4-甲氧基-3-(4-甲基-1-哌嗪基)苯基]-2'-甲基-4'-(5-甲基-1,2,4-恶二唑-3-基)[1,1-联苯]-4-甲酰胺)和PAPP(对氨基苯乙基间三氟甲基苯基哌嗪;两种化合物均腹腔注射1mg/kg,提前30分钟给药)可阻断此反应,而α1肾上腺素能受体阻滞剂哌唑嗪(腹腔注射1mg/kg)和5-HT1A受体拮抗剂SDZ 216-525(4-(-[4-(1,1,3-三氧代-2H-1,2-苯并异噻唑-2-基)丁基]-1-哌嗪基)-1H-吲哚-2-羧酸甲酯;腹腔注射1mg/kg)则无此作用。另一种α1肾上腺素能受体激动剂St 587(2-(2-氯-5-三氟甲基苯基亚氨基)-咪唑啉;腹腔注射1mg/kg)未改变体温。SDZ NVI-085诱导的豚鼠体温过低可能是由5-HT1D受体介导的。

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