GABAergic contribution to rat bladder hyperactivity after middle cerebral artery occlusion

• Published in: American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2000-10, Vol.279 (4), p.1230-R1238
• Main Authors: Kanie, Sayoko, Yokoyama, Osamu, Komatsu, Kazuto, Kodama, Koichi, Yotsuyanagi, Satoshi, Niikura, Susumu, Nagasaka, Yasuhiro, Miyamoto, Ken-Ichi, Namiki, Mikio
• Format: Article
• Language: English
• Subjects: Animals; Baclofen - administration & dosage; Baclofen - pharmacology; Bicuculline - administration & dosage; Bicuculline - pharmacology; Cerebral Infarction - physiopathology; Cerebral Ventricles - drug effects; Cerebral Ventricles - physiology; Cerebral Ventricles - physiopathology; Dose-Response Relationship, Drug; Female; GABA-A Receptor Agonists; GABA-B Receptor Agonists; Injections, Intraventricular; Middle Cerebral Artery - physiology; Muscimol - administration & dosage; Muscimol - pharmacology; Pressure; Rats; Rats, Sprague-Dawley; Seizures - physiopathology; Urinary Bladder - drug effects; Urinary Bladder - physiology; Urinary Bladder - physiopathology; Urination - drug effects; Urination - physiology
• ISSN: 0363-6119; 1522-1490
• DOI: 10.1152/ajpregu.2000.279.4.r1230

1  Department of Urology, Kanazawa University School of Medicine, and 2  Department of Pharmacology and Pharmaceutics, Graduate School of Natural Science and Technology, Kanazawa University, Ishikawa 920-8641, Japan To evaluate the influences of -aminobutyric acid (GABA) mechanisms on bladder hyperactivity after left middle cerebral artery occlusion, cystometric recordings were obtained from unanesthetized female rats. Intracerebroventricular administration of both muscimol (GABA A receptor agonist; 0.1-10 nmol) and baclofen (GABA B receptor agonist; 0.1-3 nmol) produced dose-dependent inhibitions of micturition with increases in bladder capacity (BC). The effects of high doses (1-10 nmol) were similar in sham-operated (SO) and cerebral-infarcted (CI) rats. However, lower doses of muscimol (0.1 or 0.3 nmol) and baclofen (0.1 nmol) reduced BC in CI rats. After bicuculline (GABA A receptor antagonist; 1 or 3 nmol) administration, BC in both SO and CI rats first decreased and subsequently increased. An increase in urethral pressure was observed after administration of bicuculline (3 nmol) but not with either muscimol or baclofen. Infarct volumes in muscimol-, bicuculline-, or baclofen-treated rats were not significantly different from those of vehicle-treated rats. These results suggest that GABAergic mechanisms inhibit the micturition reflex at the supraspinal level but that this can change as a result of CI. GABA or -aminobutyric acid; micturition reflex; cerebral infarction