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August 2002, Volume 14, Number 4, Pages 271-282
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Paper
Morphological and functional characterization of a rat vaginal smooth muscle sphincter
A Giraldi1,4, P Alm3, V Werkström2, L Myllymäki2, G Wagner1 and K E Andersson2

1Division of Sexual Physiology, Department of Medical Physiology, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark

2Department of Clinical Pharmacology, Lund University Hospital, Lund, Sweden

3Department of Pathology, Lund University Hospital, Lund, Sweden

4Department of Clinical Pharmacology, Rigshospitalet, Copenhagen, Denmark

Correspondence to: A Giraldi, Department of Clinical Pharmacology, Rigshospitalet, Div. 7642 Blegdamsvej 9, 2100 Copenhagen, Denmark. E-mail: giraldi@RH.dk

Abstract

The aim of the present study was to gain information about adrenergic-, cholinergic- and non-adrenergic, non-cholinergic (NANC)- transmitter systems/mediators in the rat vagina, and to characterize its smooth muscles functionally. Tissue sections from vagina of Sprague Dawley rats were immunolabelled with antibodies against protein gene product 9.5 (PGP), synaptophysin (Syn), tyrosine hydroxylase (TH), vesicular acetylcholine transporter (VAChT), neuropeptide Y (NPY), nitric oxide synthase (NOS), vasoactive intestinal polypeptide (VIP), calcitonin gene-related peptide (CGRP) and pituitary adenylate cyclase-activating polypeptide (PACAP). Circularly cut vaginal smooth muscle preparations from the distal vagina were studied in organ baths. In the paravaginal tissue, a large number of PGP-, NOS-, TH-, VIP-immunoreactive (IR) and few CGRP-IR nerve trunks were observed, giving off branches to the smooth muscle wall. The smooth muscle wall was supplied by a large number of PGP-, Syn-, VAChT-, NPY-, NOS- and TH- IR nerve terminals, whilst only a moderate to few numbers of CGRP-, VIP- and PACAP-IR terminals were identified. Especially the distal part of the vaginal wall, where the circularly running smooth muscle was thickened into a distinct sphincter structure, was very richly innervated, predominantly by PGP- and NOS-IR terminals. Below and within the basal parts of the epithelium in the distal half of the vagina, a large number of PGP- and few NOS- and PACAP-IR varicose terminals were observed. The vaginal arteries were encircled by plexuses of nerve terminals. A large number of these were PGP-, Syn-, VAChT-, NOS-, TH-, NPY- and VIP-IR, and few were CGRP- and PACAP-IR. In isolated preparations of the distal vagina, electrical field stimulation (EFS) caused frequency-dependent contractions, which were reduced by sildenafil, tetrodotoxin (TTX) and phentolamine. In preparations contracted by norepinephrine (NA), EFS produced frequency-dependent relaxations. Pretreatment with the NOS-inhibitor NG-nitro-L-arginine, TTX, or the inhibitor of soluble guanylate cyclase, ODQ, abolished the EFS relaxations. In NE precontracted preparations, cumulative addition of sildenafil caused concentration-dependent relaxation. Carbachol contracted the strips concentration-dependently from baseline. It can be concluded that the distal part of the rat vagina forms a distinct smooth muscle sphincter, which is richly innervated by adrenergic, cholinergic and NANC nerves. The present studies suggest that in the rat the L-arginine/NO-system not only plays an important role in the regulation of vaginal smooth muscle tone, but also affects blood flow, and may have sensory functions.

International Journal of Impotence Research (2002) 14, 271-282. doi:10.1038/sj.ijir.3900886

Keywords

sexual function; female; rat; smooth muscle; vagina; organ bath; immunohistochemistry

Received 27 August 2001; accepted 5 March 2002
August 2002, Volume 14, Number 4, Pages 271-282
Table of contents    Previous  Abstract  Next   Full text  PDF
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