Abstract

The effect of GABA on field stimulation (0.1 Hz) induced contractions have been examined on detrusor strips from adult and newborn rats. Field stimulation induced contractions were unaffected by hexamethonium (10(-5) M) but almost suppressed by tetrodotoxin (5 X 10(-7) M) in both age groups. Atropine (3 X 10(-6) M) produced a marked inhibition of twitches in detrusor strips from newborn rats but only a slight (10% or less) inhibition in strips from adult animals. Neither GABA (10(-4), homotaurine (10(-3) M) or (+/-)-baclofen (10(-4] affected twitches in detrusor strips from adults rats. On the other hand both GABA and (+/-)-baclofen inhibited, to about the same extent (55-60% inhibition) twitches in detrusor strips from newborn animals. Homotaurine had no significant effect. The effects of both GABA (10(-4) M) and (+/-)-baclofen (10(-4) M) on twitches in detrusor strips from newborn rats were reduced if the preparations were previously exposed to a low concentration of GABA (5 X 10(-6) M) thus indicating desensitization. The inhibitory effect of GABA on twitches in newborn rats were concentration dependent in the range of 10(-7) to 10(-4) M. The GABAA receptor antagonist picrotoxin (10(-4) M) had no effect on the GABA concentration response curve whereas the GABAB receptor antagonist, homotaurine, produced an antagonism of the competitive type. The calculated pA2 value for the GABA-homotaurine interaction was 4.4 +/- 0.07. Neither GABA (10(-4) M) nor (+/-)-baclofen (10(-4) M) produced any significant inhibition of acetylcholine (2 X 10(-7) M) induced contractions of detrusor of strips from newborn rats, while atropine (3 X 10(-6) M) completely suppressed them. These results indicate that GABA inhibits field stimulation induced contractions of detrusor strips from newborn rats by activating prejunctional receptors (presumably of the GABAB subtype) which inhibit the release of acetylcholine from the postganglionic nerve endings.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.