Ask J A
Comp Biochem Physiol A Comp Physiol. 1983;76(3):543-52. doi: 10.1016/0300-9629(83)90456-5.
The cardiac adrenoceptors of lower vertebrates were characterized in atrial preparations. Adrenaline (A) potentiated the force and frequency of contraction in the spontaneously beating atria of the frog, trout and flounder and in electrically paced atrial strips from the shark. The inotropic responses of A were most pronounced at the lower temperatures for the frog and trout, while A enhanced frequency to a greater extent at higher temperatures in the frog atria. Atrial alpha-receptors activated by A at 8 degrees C could not be detected in any of the species under study. The apparent affinities for the inotropic and chronotropic responses of agonist in the frog (15 degrees C) and trout (8 degrees C) atria were: Iso greater than Sal greater than or equal to A greater than NA. A cocaine-sensitive uptake for A and NA was apparent in these atria, consistent with sympathetic innervation. The affinities for the catecholamines in the flounder and shark atria were not increased by cocaine, in accordance with absence of sympathetic innervation of the atria in these species. These atria were also insensitive to corticosterone. The affinities for A and NA were on the other hand higher in the sympathetically non-innervated atria of the flounder than in the innervated atria of the frog and trout. The apparent orders of relative affinities for agonists were Iso greater than A = NA greater than Sal for the flounder, and of the relative potencies Iso = A greater than NA greater than Sal for the shark atrium. The results are consistent with the hypothesis that catecholamines enhance cardiac performance in lower vertebrates chiefly via "adrenaline" receptors which resemble the beta 2-type of mammalian adrenoceptors in many respects. Unlike that in mammals, cardiac adrenaline receptors in the frog and trout are activated by the sympathetic neurotransmitter ("innervated" receptors). On the other hand, the adrenaline receptors of the flounder and shark are responding to the circulating catecholamines ("humoral" receptors). However, the flounder atrium, with equal affinities for A and NA, appears as an exception to the rule by having a mixed population of humoral beta 1- and beta 2-adrenoceptors, indicating a role for circulating NA in cardiac regulation in this species.
低等脊椎动物的心脏肾上腺素能受体是在心房标本中得以鉴定的。肾上腺素(A)增强了青蛙、鳟鱼和比目鱼自发性搏动心房以及鲨鱼电刺激起搏心房条带的收缩力和频率。青蛙和鳟鱼在较低温度时,A的变力反应最为明显,而在青蛙心房中,A在较高温度下对频率的增强作用更大。在8摄氏度时被A激活的心房α受体,在所研究的任何物种中均未检测到。青蛙(15摄氏度)和鳟鱼(8摄氏度)心房中激动剂对变力和变时反应的表观亲和力为:异肾上腺素大于沙丁胺醇大于或等于肾上腺素大于去甲肾上腺素。在这些心房中,A和去甲肾上腺素对可卡因敏感的摄取很明显,这与交感神经支配一致。比目鱼和鲨鱼心房中儿茶酚胺的亲和力不会因可卡因而增加,这与这些物种心房缺乏交感神经支配一致。这些心房对皮质酮也不敏感。另一方面,比目鱼交感神经未支配的心房中对A和去甲肾上腺素的亲和力高于青蛙和鳟鱼受支配的心房。比目鱼激动剂相对亲和力的表观顺序为异肾上腺素大于肾上腺素=去甲肾上腺素大于沙丁胺醇,鲨鱼心房的相对效价顺序为异肾上腺素=肾上腺素大于去甲肾上腺素大于沙丁胺醇。这些结果与以下假设一致,即儿茶酚胺主要通过“肾上腺素”受体增强低等脊椎动物的心脏功能,这些受体在许多方面类似于哺乳动物β2型肾上腺素能受体。与哺乳动物不同,青蛙和鳟鱼的心脏肾上腺素能受体由交感神经递质激活(“受支配”受体)。另一方面,比目鱼和鲨鱼的肾上腺素能受体对循环中的儿茶酚胺有反应(“体液”受体)。然而,比目鱼心房对A和去甲肾上腺素具有相同的亲和力,似乎是个例外,因为它有混合的体液β1和β2肾上腺素能受体群体,这表明循环中的去甲肾上腺素在该物种心脏调节中起作用。