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马结肠中α2肾上腺素能受体介导的反应。

Colonic alpha 2-adrenoceptor-mediated responses in the pony.

作者信息

Roger T, Ruckebusch Y

机构信息

Department of Physiology, National Veterinary School, Toulouse, France.

出版信息

J Vet Pharmacol Ther. 1987 Dec;10(4):310-8. doi: 10.1111/j.1365-2885.1987.tb00107.x.

Abstract

The motor responses of the caecum and colon to stimulation of alpha 2-adrenoceptors by xylazine and detomidine at the recommended dose levels of 0.6 and 0.1 mg/kg were investigated in three ponies. The motor changes of the left ventral colon induced by continuous intra-arterial infusion of a prostaglandin (PGF2 alpha) were used to assess the relative inhibitory effects of xylazine and detomidine in a colic model. The administration of alpha 2-agonists inhibited the spiking activity on the whole of the large intestine for 20-30 min (xylazine) or 2-3 h (detomidine). However, the detomidine-induced inhibition was preceded by a short period of increased smooth muscle basal tone as indicated by strain-gauge force transducer measurements. This pattern of activity was neither reversed nor prevented by the administration of tolazoline (10 micrograms/kg/min) intra-arterially. In contrast, inhibition of the colonic phasic and tonic motor activity by alpha 2-adrenoceptor stimulation was reversed competitively by tolazoline. The intra-arterial infusion of prostaglandin F2 alpha (10 micrograms/kg/min) induced prolonged and sustained spiking activity that might be related to signs of mild colic. Detomidine, and to a lesser extent xylazine, relaxed the whole of the large intestine and this was accompanied by alleviation of the signs of visceral pain.

摘要

在3匹矮种马中研究了按推荐剂量0.6和0.1mg/kg给予赛拉嗪和地托咪定对盲肠和结肠α2-肾上腺素能受体刺激的运动反应。通过持续动脉内输注前列腺素(PGF2α)诱导左腹侧结肠的运动变化,以评估赛拉嗪和地托咪定在绞痛模型中的相对抑制作用。给予α2-激动剂可抑制整个大肠的峰电位活动20 - 30分钟(赛拉嗪)或2 - 3小时(地托咪定)。然而,如应变片力传感器测量所示,地托咪定诱导的抑制之前有一段短时间的平滑肌基础张力增加。这种活动模式既未被动脉内给予妥拉唑啉(10微克/千克/分钟)逆转,也未被阻止。相反,α2-肾上腺素能受体刺激对结肠相性和紧张性运动活动的抑制可被妥拉唑啉竞争性逆转。动脉内输注前列腺素F2α(10微克/千克/分钟)诱导了可能与轻度绞痛体征相关的延长且持续的峰电位活动。地托咪定以及在较小程度上的赛拉嗪可使整个大肠松弛,这伴随着内脏疼痛体征的减轻。

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