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DOI 10.1152/ajpendo.1995.269.1.e108

Медицинская библиотека · The American journal of physiology · 1995

Pituitary adenylate cyclase-activating polypeptide: occurrence and relaxant effect in female genital tract.

Steenstrup B R, Alm P, Hannibal J, Jørgensen J C, Palle C, Junge J, Christensen H B, Ottesen B, Fahrenkrug J

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The distribution, localization, and smooth muscle effects of pituitary adenylate cyclase-activating polypeptide (PACAP) were studied in the human female genital tract. The concentrations of PACAP-38 and PACAP-27 were measured by radioimmunoassays, and both peptides were found throughout the genital tract. The highest concentrations of PACAP-38 were detected in the ovary, the upper part of vagina, and the perineum. The concentrations of PACAP-27 were generally low, in some regions below the detection limit and in other regions 1 to 5% of the PACAP-38 concentrations. Immunocytochemistry revealed that PACAP was located in delicate varicose nerve fibers that were most abundant in the internal cervical os, where they mainly seemed to innervate blood vessels and smooth muscle cells. PACAP-38 and PACAP-27 (10(-10)-10(-6) M) caused a concentration-dependent relaxation of the spontaneous activity of the nonvascular smooth muscle strips from fallopian tube and myometrium in vitro. Likewise, both peptides (10(-10)-10(-6) M) caused relaxation of nonrepinephrine (10(-6) M)-precontracted intramyometrial arteries. No effect of the PACAP sequences, PACAP-(6-27), PACAP-(16-38), and PACAP-(18-27), on fallopian tube was observed. The findings suggest a smooth muscle regulatory role of PACAP in the human female reproductive tract.

Для цитирования: Steenstrup B R, Alm P, Hannibal J, Jørgensen J C, Palle C, Junge J, Christensen H B, Ottesen B, Fahrenkrug J. Pituitary adenylate cyclase-activating polypeptide: occurrence and relaxant effect in female genital tract.. The American journal of physiology. 1995. DOI: 10.1152/ajpendo.1995.269.1.e108.

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