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. 1989 Aug;97(4):1292–1296. doi: 10.1111/j.1476-5381.1989.tb12591.x

3-Aminopropylphosphinic acid--a potent, selective GABAB receptor agonist in the guinea-pig ileum and rat anococcygeus muscle.

J M Hills 1, R A Dingsdale 1, M E Parsons 1, R E Dolle 1, W Howson 1
PMCID: PMC1854597  PMID: 2551445

Abstract

1. 3-Aminopropylphosphinic acid, a gamma-aminobutyric acid (GABA) analogue, was tested for activity on guinea-pig isolated ileum and rat isolated anococcygeus muscle preparations. The effects of 3-aminopropylphosphinic acid were compared with those of GABA and baclofen. 2. In the electrically stimulated ileum, 3-aminopropylphosphinic acid, like GABA and baclofen, caused a concentration-dependent inhibition of the cholinergic twitch contraction, the IC50 value being 1.84 +/- 0.23 microM (n = 12). Unlike GABA, but like baclofen, 3-aminopropylphosphinic acid did not produce an initial contraction. 3. The inhibitory effects of 3-aminopropylphosphinic acid and baclofen in the guinea-pig ileum were not significantly antagonized by bicuculline (10 microM), phentolamine plus propranolol (both 1 microM), yohimbine (1 microM), naloxone (1 microM), impromidine (1 microM) or 8-phenyltheophylline (10 microM). The inhibitory effects of 3-aminopropylphosphinic acid, but not of baclofen, were however antagonized by phaclofen (500 microM). In addition the effects of 3-aminopropylphosphinic acid were abolished by baclofen desensitization in the guinea-pig ileum. 4. 3-Aminopropylphosphinic acid, GABA and baclofen reduced the twitch contraction evoked by electrical field stimulation in the rat anococcygeus muscle. The IC50 for 3-aminopropylphosphinic acid inhibition of the anococcygeus contraction was 0.89 +/- 0.15 microM (n = 8). 5. It is concluded that 3-aminopropylphosphinic acid is a potent, selective GABAB agonist, being seven times more potent than baclofen in the guinea-pig ileum and five times more potent than baclofen in the rat anococcygues muscle preparations.

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Selected References

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  1. BULBRING E. Measurements of oxygen consumption in smooth muscle. J Physiol. 1953 Oct;122(1):111–134. doi: 10.1113/jphysiol.1953.sp004983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bowery N. G., Doble A., Hill D. R., Hudson A. L., Shaw J. S., Turnbull M. J., Warrington R. Bicuculline-insensitive GABA receptors on peripheral autonomic nerve terminals. Eur J Pharmacol. 1981 Apr 24;71(1):53–70. doi: 10.1016/0014-2999(81)90386-1. [DOI] [PubMed] [Google Scholar]
  3. Dutar P., Nicoll R. A. A physiological role for GABAB receptors in the central nervous system. Nature. 1988 Mar 10;332(6160):156–158. doi: 10.1038/332156a0. [DOI] [PubMed] [Google Scholar]
  4. Gillespie J. S. The rat anococcygeus muscle and its response to nerve stimulation and to some drugs. Br J Pharmacol. 1972 Jul;45(3):404–416. doi: 10.1111/j.1476-5381.1972.tb08097.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Giotti A., Luzzi S., Spagnesi S., Zilletti L. GABAA and GABAB receptor-mediated effects in guinea-pig ileum. Br J Pharmacol. 1983 Mar;78(3):469–478. doi: 10.1111/j.1476-5381.1983.tb08807.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kaplita P. V., Waters D. H., Triggle D. J. gamma-Aminobutyric acid action in guinea-pig ileal myenteric plexus. Eur J Pharmacol. 1982 Apr 8;79(1-2):43–51. doi: 10.1016/0014-2999(82)90573-8. [DOI] [PubMed] [Google Scholar]
  7. Karlsson G., Pozza M., Olpe H. R. Phaclofen: a GABAB blocker reduces long-duration inhibition in the neocortex. Eur J Pharmacol. 1988 Apr 13;148(3):485–486. doi: 10.1016/0014-2999(88)90136-7. [DOI] [PubMed] [Google Scholar]
  8. Kerr D. I., Ong J., Prager R. H., Gynther B. D., Curtis D. R. Phaclofen: a peripheral and central baclofen antagonist. Brain Res. 1987 Mar 3;405(1):150–154. doi: 10.1016/0006-8993(87)90999-1. [DOI] [PubMed] [Google Scholar]
  9. Krantis A., Costa M., Furness J. B., Orbach J. gamma-Aminobutyric acid stimulates intrinsic inhibitory and excitatory nerves in the guinea-pig intestine. Eur J Pharmacol. 1980 Oct 31;67(4):461–468. doi: 10.1016/0014-2999(80)90187-9. [DOI] [PubMed] [Google Scholar]
  10. Krogsgaard-Larsen P. GABA synaptic mechanisms: stereochemical and conformational requirements. Med Res Rev. 1988 Jan-Mar;8(1):27–56. doi: 10.1002/med.2610080103. [DOI] [PubMed] [Google Scholar]
  11. Luzzi S., Franchi-Micheli S., Ciuffi M., Pajani A., Zilletti L. GABA-related activities of amino phosphonic acids on guinea-pig ileum longitudinal muscle. J Auton Pharmacol. 1986 Sep;6(3):163–169. doi: 10.1111/j.1474-8673.1986.tb00641.x. [DOI] [PubMed] [Google Scholar]
  12. Muhyaddin M., Roberts P. J., Woodruff G. N. Presynaptic gamma-aminobutyric acid receptors in the rat anococcygeus muscle and their antagonism by 5-aminovaleric acid. Br J Pharmacol. 1982 Sep;77(1):163–168. doi: 10.1111/j.1476-5381.1982.tb09282.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ong J., Kerr D. I. GABAA- and GABAB-receptor-mediated modification of intestinal motility. Eur J Pharmacol. 1982 Dec 17;86(1):9–17. doi: 10.1016/0014-2999(82)90390-9. [DOI] [PubMed] [Google Scholar]
  14. Soltesz I., Haby M., Leresche N., Crunelli V. The GABAB antagonist phaclofen inhibits the late K+-dependent IPSP in cat and rat thalamic and hippocampal neurones. Brain Res. 1988 May 17;448(2):351–354. doi: 10.1016/0006-8993(88)91275-9. [DOI] [PubMed] [Google Scholar]

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