EFFECTS OF TRANSMURAL FIELD STIMULATION IN ISOLATED SMOOTH-MUSCLE OF HUMAN RECTUM AND INTERNAL ANAL-SPHINCTER

Citation
Eb. Glavind et al., EFFECTS OF TRANSMURAL FIELD STIMULATION IN ISOLATED SMOOTH-MUSCLE OF HUMAN RECTUM AND INTERNAL ANAL-SPHINCTER, American journal of physiology: Gastrointestinal and liver physiology, 35(5), 1997, pp. 1075-1082
Citations number
40
Categorie Soggetti
Physiology
ISSN journal
01931857
Volume
35
Issue
5
Year of publication
1997
Pages
1075 - 1082
Database
ISI
SICI code
0193-1857(1997)35:5<1075:EOTFSI>2.0.ZU;2-1
Abstract
Smooth muscle preparations from the circular muscle layer of the most distal rectum and the proximal and distal human internal anal sphincte r (IAS) mounted in organ baths to record isometric tension developed s pontaneous tension. Transmural electrical field stimulation (TMS) indu ced frequency- and impulse duration-dependent relaxations sensitive to tetrodotoxin in the stimulation range of 0.5-40 Hz and 0.04-0.6 ms. P oststimulus contractions were most frequent and prominent in rectal pr eparations. Maximal relaxations were comparable in the three locations and were achieved at 10 Hz and 0.4 ms. The frequency inducing half-ma ximal response was lower in rectal strips compared with LAS. Phentolam ine (10(-6) M) enhanced relaxations and diminished off-contractions at 40 Hz in distal LAS. N-omega-nitro-L-arginine (L-NNA) concentration d ependently inhibited both relaxations and off-contractions (10 Hz, 0.4 ms). The pD(2) values (-log EC50) Of L-NNA were lower in rectal muscl e compared with those in IAS. L-Arginine (10(-4) M) inhibited the bloc king effect of L-NNA. In one-half of the preparations, L-NNA reversed the relaxations to duration contractions (15-40 Hz), which were inhibi ted by atropine in rectal preparations and by phentolamine in LAS. In conclusion, excitatory innervation of the LAS is alpha-adrenergic and cholinergic in the rectum. A product of the L-arginine-nitric oxide pa thway mediates the TMS-induced inhibition of the muscle and is also in volved in poststimulus contractions.