首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >The effects of intraperitoneal administration of antagonists and development of morphine tolerance on the antinociception induced by stimulating the anterior pretectal nucleus of the rat.
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The effects of intraperitoneal administration of antagonists and development of morphine tolerance on the antinociception induced by stimulating the anterior pretectal nucleus of the rat.

机译:腹膜内施用拮抗剂和吗啡耐受性的发展对刺激大鼠前棘前核诱导的抗伤害感受的影响。

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摘要

1 The effects of intraperitoneal administration of antagonists to morphine, 5-hydroxytryptamine (5-HT), noradrenaline and dopamine have been studied on the antinociceptive effects of electrical stimulation of the anterior pretectal nucleus (APtN) of the rat. 2 A 15 s period of 35 microA sine wave stimulation of APtN significantly increased the latency of the tail flick reflex to noxious heat for periods up to 1 h. 3 Naloxone (0.25-1.0 mg kg-1) attenuated the effects of APtN stimulation in a dose-dependent manner. In rats made tolerant to morphine by daily administration of morphine, the antinociceptive effects of APtN stimulation were significantly reduced. 4 The 5-HT receptor antagonists methysergide (5 mg kg-1) and ketanserin (1 mg kg-1), the dopamine receptor antagonist haloperidol (1 mg kg-1) and the beta-adrenoceptor antagonist propranolol (1 mg kg-1) had little effect on the antinociceptive effects of stimulating the APtN. 5 alpha-Adrenoceptor antagonists caused a dose-dependent antagonism of the response. The order of potency was; idazoxan greater than prazosin greater than phenoxybenzamine, the respective ED50 for each drug being 0.08: 0.45: 1.5 mg kg-1. 6 It is concluded that antagonism at opioid receptors and alpha-adrenoceptors but not beta-adrenoceptors, dopamine or 5-HT receptors reduces the antinociceptive effects of APtN stimulation. This differs from the reported effects of these antagonists on the antinociception caused by stimulating other sites in the brain.
机译:1已研究了腹膜内给予吗啡,5-羟色胺(5-HT),去甲肾上腺素和多巴胺拮抗剂对大鼠电刺激大鼠前棘前核(APtN)的镇痛作用。 2在15 s的35 microA正弦波刺激APtN的过程中,显着增加了尾部轻弹反射对有害热量的潜伏期,长达1 h。 3纳洛酮(0.25-1.0 mg kg-1)以剂量依赖性方式减弱APtN刺激的作用。在每天服用吗啡可耐受吗啡的大鼠中,APtN刺激的抗伤害感受作用显着降低。 4 5-HT受体拮抗剂美塞麦肽(5 mg kg-1)和酮色林(1 mg kg-1),多巴胺受体拮抗剂氟哌啶醇(1 mg kg-1)和β-肾上腺素受体拮抗剂普萘洛尔(1 mg kg-1) )对刺激APtN的镇痛作用几乎没有作用。 5种α-肾上腺素受体拮抗剂引起反应的剂量依赖性拮抗作用。有力的顺序是;大于唑吡星大于苯氧苄星的吡唑啉酮,每种药物的ED50为0.08:0.45:1.5 mg kg-1。 6结论是,阿片受体和α-肾上腺素受体而不是β-肾上腺素受体,多巴胺或5-HT受体的拮抗作用降低了APtN刺激的抗伤害感受作用。这与这些拮抗剂对刺激大脑中其他部位引起的抗伤害感受的报道作用不同。

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