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大鼠和豚鼠输精管中兴奋性多巴胺受体的存在情况。

Occurrence of excitatory dopaminoceptors in the rat and guinea-pig vas deferens.

作者信息

Tayo F M

出版信息

Clin Exp Pharmacol Physiol. 1979 May-Jun;6(3):275-9. doi: 10.1111/j.1440-1681.1979.tb01249.x.

Abstract
  1. Noradrenaline and dopamine produce contractions of isolated preparations of vasa deferentia from the rat or the guinea-pig. 2. Dopamine was three to five times as potent as noradrenaline on the rat vas deferens, but was considerably less potent than noradrenaline on the guinea-pig vas deferens. 3. Phentolamine antagonized responses to noradrenaline and dopamine of vasa deferentia of both species. On the rat vas deferens the pA2 values against noradrenaline and dopamine were 7.6 and 7.4, respectively. 4. Pimozide, a dopamine antagonist, antagonized responses to dopamine on vasa deferentia of both species, but was not significantly active in antagonizing responses to noradrenaline. On the rat vas deferens, the pA2 value against dopamine was 7.9. t. The beta-adrenoceptor blocking agents, propranolol and oxprenolol slightly enhanced dopamine-induced contractions on vasa deferentia of both species. 6. It is suggested that dopamine might act on both a-adrenoceptors and dopaminoceptors in the vas deferens, and that the component due to activation of dopaminoceptors is greater in the rat than the guinea-pig.
摘要
  1. 去甲肾上腺素和多巴胺可使大鼠或豚鼠的离体输精管产生收缩。2. 多巴胺对大鼠输精管的作用强度是去甲肾上腺素的三到五倍,但对豚鼠输精管的作用强度远低于去甲肾上腺素。3. 酚妥拉明可拮抗这两种动物输精管对去甲肾上腺素和多巴胺的反应。在大鼠输精管上,对抗去甲肾上腺素和多巴胺的pA2值分别为7.6和7.4。4. 多巴胺拮抗剂匹莫齐特可拮抗这两种动物输精管对多巴胺的反应,但在拮抗对去甲肾上腺素的反应方面无明显活性。在大鼠输精管上,对抗多巴胺的pA2值为7.9。5. β肾上腺素受体阻断剂普萘洛尔和氧烯洛尔可轻微增强这两种动物输精管上多巴胺诱导的收缩。6. 提示多巴胺可能作用于输精管的α肾上腺素受体和多巴胺受体,且大鼠输精管中因多巴胺受体激活产生的作用成分比豚鼠的更大。

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