VASOACTIVE INTESTINAL POLYPEPTIDE (VIP) AND PEPTIDE HISTIDINE METHIONINE (PHM) IN HUMAN PENILE CORPUS CAVERNOSUM TISSUE AND CIRCUMFLEX VEINS - LOCALIZATION AND INVITRO EFFECTS

被引:16
作者
KIRKEBY, HJ
FAHRENKRUG, J
HOLMQUIST, F
OTTESEN, B
机构
[1] AARHUS UNIV HOSP,DEPT OBSTET & GYNECOL,DK-8000 AARHUS,DENMARK
[2] AARHUS UNIV HOSP,DEPT UROL,DK-8000 AARHUS,DENMARK
[3] UNIV COPENHAGEN,BISPEBJERG HOSP,DEPT CLIN BIOCHEM,DK-1168 COPENHAGEN,DENMARK
[4] UNIV LUND HOSP,DEPT CLIN PHARMACOL,S-22185 LUND,SWEDEN
[5] HERLEV UNIV HOSP,DEPT OBSTET & GYNECOL,COPENHAGEN,DENMARK
[6] STATENS SERUM INST,MOLEC CELL BIOL LAB,DK-2300 COPENHAGEN,DENMARK
关键词
ERECTION; PENILE VENOUS OUTFLOW REGULATION; PEPTIDES; PEPTIDE HISTIDINE METHIONINE; VASOACTIVE INTESTINAL POLYPEPTIDE;
D O I
10.1111/j.1365-2362.1992.tb01931.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Localization and functional effects of vasoactive intestinal polypeptide (VIP) and peptide histidine methionine (PHM), two peptides derived from a common precursor molecule, were investigated in isolated preparations from human penile corpus cavernosum (CC) and circumflex vein (CV). VIP- and PHM-immunoreactivity (IR) was demonstrated in both CC and CV. The concentrations of VIP-IR and PHM-IR in CC tissue were 54.4 +/- 15.3, and 42.0 +/- 7.5 pmol g-1 wet weight respectively with a VIP/PHM ratio of 1.5 +/- 0.4 (mean +/- SEM). The corresponding values for CV tissues were 28.0 +/- 7.7 and 9.6 +/- 2.6 pmol g-1 wet weight with a VIP/PHM ratio of 3.1 +/- 0.4. CC and CV displayed VIP- and PHM-IR confined to nerve fibres in close relation to bundles of smooth muscle cells and blood vessels in both tissues. In vitro, VIP and PHM had no effects in unstimulated tissue preparations. Both peptides concentration-dependently (10(-9)-10(-6) M) relaxed CC and CV preparations precontracted with 3 x 10(-6) M noradrenaline. In CC the maximum relaxant effect of VIP and PHM was 22 +/- 11% and 9 +/- 9% and in CV the corresponding values were 82 +/- 8% and 93 +/- 3% respectively. The present study supports the hypothesis of VIP and PHM as neurotransmitters and/or neuromodulators in the nervous control of penile erection.
引用
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页码:24 / 30
页数:7
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