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犬后肢血管舒张性多巴胺受体的定位

Localization of vasodilator dopamine receptors in the canine hindlimb.

作者信息

Bell C, Stubbs A

出版信息

Br J Pharmacol. 1978 Oct;64(2):253-7. doi: 10.1111/j.1476-5381.1978.tb17297.x.

Abstract

1 Vascular responses to local injection of dopamine and isoprenaline have been compared in the blood-perfused gracilis muscle and hind paw pads of dogs anaesthetized with chloralose. 2 In the paw pads, dopamine (0.5 to 5.0 microgram) caused a transient vasoconstriction followed by dose-dependent vasodilatation. alpha-Adrenoceptor blockade converted this response to pure vasodilatation, which was attenuated or abolished by the dopamine-receptor antagonist, haloperidol (1 to 2 mg i.a.). In the gracilis, dopamine produced only vasoconstriction. Following alpha-adrenoceptor blockade this was abolished, but only a very small dilator response was revealed. 3 Isoprenaline (0.05 to 0.5 microgram) caused dose-dependent dilatation in both beds, which was attenuated by propranolol (0.1 mg/kg i.v.). 4 Glyceryl trinitrate (0.2 to 5.0 microgram) was used to assess vascular reactivity. When responses to isoprenaline and dopamine were compared with those to glyceryl trinitrate, both beds had approximately equal reactivity to isoprenaline. In contrast the paw pads were 10 fold more responsive to dopamine than was the gracilis. 5 We conclude that the vessels of the paw pads play an important part in the femoral dilator response to dopamine.

摘要
  1. 在用氯醛糖麻醉的犬的血液灌注股薄肌和后爪垫中,比较了对局部注射多巴胺和异丙肾上腺素的血管反应。2. 在爪垫中,多巴胺(0.5至5.0微克)引起短暂的血管收缩,随后是剂量依赖性血管舒张。α-肾上腺素能受体阻断将这种反应转变为单纯的血管舒张,而多巴胺受体拮抗剂氟哌啶醇(1至2毫克腹腔注射)可减弱或消除这种反应。在股薄肌中,多巴胺仅产生血管收缩。α-肾上腺素能受体阻断后这种收缩被消除,但仅显示出非常小的舒张反应。3. 异丙肾上腺素(0.05至0.5微克)在两个部位均引起剂量依赖性舒张,普萘洛尔(0.1毫克/千克静脉注射)可减弱这种舒张。4. 硝酸甘油(0.2至5.0微克)用于评估血管反应性。当将对异丙肾上腺素和多巴胺的反应与对硝酸甘油的反应进行比较时,两个部位对异丙肾上腺素的反应性大致相等。相比之下,爪垫对多巴胺的反应性比股薄肌高10倍。5. 我们得出结论,爪垫血管在股部对多巴胺的舒张反应中起重要作用。

相似文献

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Vascular dopamine receptors in the canine hindlimb.犬后肢的血管多巴胺受体
Br J Pharmacol. 1975 Oct;55(2):167-72. doi: 10.1111/j.1476-5381.1975.tb07625.x.

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