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吗啡、H-酪氨酰-D-精氨酰-苯丙氨酰-赖氨酰胺(DALDA)和B-HT920对脊髓麻醉豚鼠非胆碱能神经介导的支气管收缩的影响。

Effects of morphine, H-Tyr-D-Arg-Phe-Lys-NH2 (DALDA) and B-HT920 on non-cholinergic nerve-mediated bronchoconstriction in pithed guinea-pigs.

作者信息

Rechtman M P, Boura A L, King R G, Olley J E, Schiller P W

机构信息

Department of Pharmacology, Monash University, Clayton, Victoria, Australia.

出版信息

Br J Pharmacol. 1990 Oct;101(2):269-72. doi: 10.1111/j.1476-5381.1990.tb12699.x.

Abstract
  1. Electrical stimulation (1 ms, 5 Hz, 80 V) for 5 or 15 s at the level of C4-T1 in the spinal canal of artificially respired pithed guinea-pigs (which had received intravenously (i.v.) (+)-tubocurarine chloride 2 mg kg-1, atropine sulphate 2 mg kg-1 and pentolinium tartrate 5 mg kg-1) caused constriction of airways, indicated by increased insufflation pressure. 2. This non-cholinergic constriction was inhibited by morphine (1-3 mg kg-1, i.v.), the peripherally acting mu-receptor agonist, H-Tyr-D-Arg-Phe-Lys-NH2 (DALDA, 0.1-1 mg kg-1, i.v.) or the alpha 2-adrenoceptor agonist B-HT920 (1-3 mg kg-1, i.v.). 3. The effects of either morphine (3 mg kg-1, i.v.) or DALDA (1 mg kg-1, i.v.) were inhibited by naloxone (3 mg kg-1, i.v.). Idazoxan (3 mg kg-1, i.v.) inhibited the anti-constrictor effect of B-HT920 (3 mg kg-1, i.v.), but not that of DALDA (0.1 mg kg-1, i.v.). 4. Thus activation of peripheral mu-opioid receptors or alpha 2-adrenoceptors inhibits airways constriction induced by non-cholinergic nerve stimulation in the pithed guinea-pig. This preparation therefore provides a further method for the in vivo examination of the effects of drugs on non-cholinergic tracheobronchial constrictor nerve function.
摘要
  1. 对人工呼吸的脊髓被破坏的豚鼠(静脉注射2 mg/kg氯化筒箭毒碱、2 mg/kg硫酸阿托品和5 mg/kg酒石酸喷托铵)在C4 - T1脊髓水平进行1毫秒、5赫兹、80伏的电刺激5或15秒,会导致气道收缩,表现为吹入压力增加。2. 这种非胆碱能性收缩被吗啡(1 - 3 mg/kg,静脉注射)、外周作用的μ受体激动剂H - Tyr - D - Arg - Phe - Lys - NH2(DALDA,0.1 - 1 mg/kg,静脉注射)或α2肾上腺素能受体激动剂B - HT920(1 - 3 mg/kg,静脉注射)抑制。3. 吗啡(3 mg/kg,静脉注射)或DALDA(1 mg/kg,静脉注射)的作用被纳洛酮(3 mg/kg,静脉注射)抑制。咪唑克生(3 mg/kg,静脉注射)抑制B - HT920(3 mg/kg,静脉注射)的抗收缩作用,但不抑制DALDA(0.1 mg/kg,静脉注射)的作用。4. 因此,外周μ阿片受体或α2肾上腺素能受体的激活抑制了脊髓被破坏的豚鼠中非胆碱能神经刺激诱导的气道收缩。所以该制备方法为体内检测药物对非胆碱能气管支气管收缩神经功能的影响提供了另一种方法。

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Sensory nerves in the airways as a target for drug development.气道中的感觉神经作为药物开发的靶点。
Clin Exp Pharmacol Physiol. 1992 Jan;19(1):31-9. doi: 10.1111/j.1440-1681.1992.tb00394.x.

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