Ackerly J A, Moore A F, Peach M J
Proc Natl Acad Sci U S A. 1977 Dec;74(12):5725-8. doi: 10.1073/pnas.74.12.5725.
Evidence of selective inhibition, differences in dose-response relationships, and cross-tachyphylaxis studies suggest that separate receptors and/or mechanisms may be involved in responses to angiotensin (Ang), [Sar1]Ang II, and Ang III (= des-Asp1-Ang II). The extracellular Ca2+ requirement for contractile responses induced by angiotensin peptides and norepinephrine was determined in rabbit aortic strips. Responses to K+ and [Sar1]Ang II were attenuated markedly by treatment with SKF-525A, verapamil, or Ca2+-free buffer. The response to Ang II was not impaired by verapamil, was blocked partially by SKF-525A, and was reduced markedly in Ca2+-free medium. Norepinephrine- and Ang III-induced contractions were not dependent on extracellular Ca2+. K+, Ang II, and [Sar1]Ang II required extracellular Ca2+ to induce contraction of the rabbit aorta. The data indicate that Ang III may have a mechanism of action that differs from that of [Sar1]Ang II and Ang II.
选择性抑制的证据、剂量反应关系的差异以及交叉快速耐受性研究表明,对血管紧张素(Ang)、[Sar1]Ang II和Ang III(=去天冬氨酸1 - Ang II)的反应可能涉及不同的受体和/或机制。在兔主动脉条中测定了血管紧张素肽和去甲肾上腺素诱导收缩反应所需的细胞外Ca2+。用SKF - 525A、维拉帕米或无Ca2+缓冲液处理后,对K+和[Sar1]Ang II的反应明显减弱。维拉帕米不损害对Ang II的反应,SKF - 525A部分阻断该反应,在无Ca2+培养基中该反应明显降低。去甲肾上腺素和Ang III诱导的收缩不依赖于细胞外Ca2+。K+、Ang II和[Sar1]Ang II需要细胞外Ca2+来诱导兔主动脉收缩。数据表明,Ang III的作用机制可能与[Sar1]Ang II和Ang II不同。