|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Departments of 1Urology, 3Physical Medicine and Rehabilitation, 4Obstetrics and Gynecology, and 10Neurology, Chung-Shan Medical University Hospital, 2Institute of Medicine and 6Department of Physiology, College of Medicine, Chung-Shan Medical University, 5Division of Urology, Department of Surgery, Taichung Veterans General Hospital, and 7Department of Veterinary Medicine, College of Veterinary Medicine, 8Department of Life Science, Chung-Hsing University, Taichung; 9Department of Obstetrics and Gynecology, Chung-Gang Medical University Hospital, and 11Medical Department, Saint Paul's Hospital, Taoyuan; and 12Graduate Institute of Biomedical Electronics and Bioinformatics, National Taiwan University, Taipei, Taiwan
Submitted 15 April 2008 ; accepted in final form 10 July 2008
The impact of acute anal stretch on the pelvic-urethra reflex potentiation was examined in urethane-anesthetized rats by recording the external urethra sphincter electromyogram activity evoked by the pelvic afferent stimulation. Test stimulation (1 stimulation/30 s) evoked a baseline reflex activity with a single action potential that was abolished by gallamine (5 mg/kg iv). On the other hand, the repetitive stimulation (1 stimulation/1 s) induced spinal reflex potentiation (SRP) that was attenuated by intrathecal 6-cyano-7-nitroquinoxaline-2,4-dione (a glutamatergic
-amino-3-hydroxy-5-methyl-4-isoxazoleproprionat receptor antagonist, 100 µM, 10 µl) and D-2-amino-5-phosphonovalerate [a glutamatergic N-methyl-D-aspartate (NMDA) antagonist, 100 µM, 10 µl]. Acute anal stretch using a mosquito clamp with a distance of 4 mm exhibited no effect, whereas distances of 8 mm attenuated and 12 mm abolished the repetitive stimulation-induced SRP. Intrathecal NMDA (100 µM, 10 µl) reversed the abolition on SRP caused by anal stretch. On the other hand, pretreated bicuculline [
-aminobutyric acid (GABA) A receptor antagonist, 100 µM, 10 µl] but not hydroxysaclofen (GABAB receptor antagonist) counteracted the abolition on the repetitive stimulation-induced SRP caused by the anal stretch. All of the results suggested that anal stretch may be used as an adjunct to assist voiding dysfunction in patients with overactive urethra sphincter and that GABAergic neurotransmission is important in the neural mechanisms underlying external urethra sphincter activity inhibited by anal stretch.
spinal cord; voiding dysfunction; glutamate; bicuculline; hydroxysaclofen
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |