首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Pituitary adenylate cyclase-activating polypeptide helospectin and vasoactive intestinal polypeptide in human corpus cavernosum.
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Pituitary adenylate cyclase-activating polypeptide helospectin and vasoactive intestinal polypeptide in human corpus cavernosum.

机译:人海绵体中的垂体腺苷酸环化酶激活多肽Helospectin和血管活性肠多肽。

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摘要

1. The distribution and effects of pituitary adenylate cyclase-activating polypeptide (PACAP-27 and -38), helospectin (Hel-1 and Hel-2), and vasoactive intestinal polypeptide (VIP), were investigated in isolated preparations of human corpus cavernosum (CC). 2. Immunohistochemistry revealed coinciding profiles of nerve structures that showed immunoreactivities for VIP and PACAP, and VIP and Hel. Confocal microscopy showed the co-existence of VIP- and PACAP-immunoreactivities, and VIP- and Hel-immunoreactivities in most (90%) varicose nerve structures. 3. As determined by radioimmunoassay, the amounts of VIP, PACAP-27, and PACAP-38 in the preparations were 61.7 +/- 11.6, 0.1 +/- 0.05, and 3.7 +/- 0.5 pmol g-1 wet weight of tissue (pmol g-1 wet wt.), respectively. In tissue from patients with diabetes, the content of VIP was lower (13.7 +/- 0.5 pmol g-1 wet wt.), whereas that of PACAP (-27 and -38) was unchanged. 4. Cyclic nucleotide levels were determined in preparations exposed to PACAP-27, PACAP-38, Hel-1, Hel-2, and VIP. All the peptides, but Hel-2, significantly increased the concentrations of cyclic AMP, whereas the levels of cyclic GMP were unchanged. 5. The peptides concentration-dependently relaxed noradrenaline-contracted preparations. The order of potency was VIP > PACAP 27 > Hel-1 > Hel-2 > PACAP-38. 6. Hel-1, VIP and PACAP-27 effectively counteracted electrically induced contractions. At 10(-6) M, the highest peptide concentration used, the inhibitory effects obtained reached 96 +/- 3%, 87 +/- 6%, and 80 +/- 3%, respectively. 7. The results suggest that PACAP and Hel-1 are co-localized with VIP in nerve structures within the human cavernous tissue, and that the peptides are effective relaxants of CC preparations in vitro.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在分离的人海绵体制剂中研究了垂体腺苷酸环化酶激活多肽(PACAP-27和-38),Helopectin(Hel-1和Hel-2)和血管活性肠多肽(VIP)的分布和作用。 (CC)。 2.免疫组织化学显示神经结构的重合,显示VIP和PACAP以及VIP和Hel的免疫反应性。共聚焦显微镜显示,在大多数(90%)曲张神经结构中,VIP和PACAP免疫反应共存,而VIP和Hel免疫反应共存。 3.通过放射免疫测定法确定,制剂中VIP,PACAP-27和PACAP-38的量为组织湿重61.7 +/- 11.6、0.1 +/- 0.05和3.7 +/- 0.5pmol g-1。 (pmol g-1湿重)。在糖尿病患者的组织中,VIP含量较低(13.7 +/- 0.5 pmol g-1湿重),而PACAP的含量(-27和-38)没有变化。 4.在暴露于PACAP-27,PACAP-38,Hel-1,Hel-2和VIP的制剂中测定环核苷酸水平。除Hel-2外,所有肽均显着增加了环状AMP的浓度,而环状GMP的水平未变。 5.肽浓度依赖性的去甲肾上腺素收缩制剂。效力的顺序为VIP> PACAP 27> Hel-1> Hel-2> PACAP-38。 6. Hel-1,VIP和PACAP-27有效抵消了电诱导的收缩。在10(-6)M(使用的最高肽浓度)下,获得的抑制作用分别达到96 +/- 3%,87 +/- 6%和80 +/- 3%。 7.结果表明,PACAP和Hel-1与VIP共同定位在人海绵体组织的神经结构中,并且该肽在体外是CC制剂的有效松弛剂。(摘要截短为250字)

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