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Allosteric interactions at L-type calcium channels between FPL 64176 and the enantiomers of the dihydropyridine Bay K 8644.
J Pharmacol Exp Ther. 1995 Nov; 275(2):638-45.JP

Abstract

Functional interactions between the enantiomers of the dihydropyridine 1,4-dihydro-2,6-dimethyl-5-nitro-4-[2-(trifluoromethyl)-phenyl]-3-pyridi ne carboxylic acid methyl ester (Bay K 8644) and the benzoylpyrrole methyl 2,5-dimethyl-4-[2(phenylmethyl)benzoyl]-H-pyrrole-3-carboxylate (FPL 64176) were investigated on L-type Ca++ channels in guinea pig ileal longitudinal smooth muscle. The effects of these drugs, when applied individually, were as described in earlier studies. For instance, both (-)-(S)-Bay K 8644 and FPL 64176 caused concentration-dependent contraction, which is consistent with Ca++ channel activation, whereas (+)-(R)-Bay K 8644 gave concentration-dependent relaxation, which is consistent with Ca++ channel inhibition. The activities of the different drugs were dependent on the extracellular levels of KCI. When applied in combination, however, the responses evoked were not those predicted from the effects of the drugs applied individually. Contractions produced by FPL 64176 (25 nM to 1 microM) were abolished in the presence of 100 nM (-)-(S)-Bay K 8644 but were potentiated by 10 to 150 nM (+)-(R)-Bay K 8644 and inhibited by 1 microM (+)-(R)-Bay K 8644. Conversely, contractile responses to (-)-(S)-Bay K 8644 were abolished by 100 nM FPL 64176. In the presence of 1 microM FPL 64176, however, (-)-(S)-Bay K 8644 gave concentration-dependent relaxation of the muscle, which is consistent with Ca++ channel inhibition.(

ABSTRACT

TRUNCATED AT 250 WORDS)

Authors+Show Affiliations

Dept. of Pharmacology, University of Bristol, United Kingdom.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

7473149

Citation

Usowicz, M M., et al. "Allosteric Interactions at L-type Calcium Channels Between FPL 64176 and the Enantiomers of the Dihydropyridine Bay K 8644." The Journal of Pharmacology and Experimental Therapeutics, vol. 275, no. 2, 1995, pp. 638-45.
Usowicz MM, Gigg M, Jones LM, et al. Allosteric interactions at L-type calcium channels between FPL 64176 and the enantiomers of the dihydropyridine Bay K 8644. J Pharmacol Exp Ther. 1995;275(2):638-45.
Usowicz, M. M., Gigg, M., Jones, L. M., Cheung, C. W., & Hartley, S. A. (1995). Allosteric interactions at L-type calcium channels between FPL 64176 and the enantiomers of the dihydropyridine Bay K 8644. The Journal of Pharmacology and Experimental Therapeutics, 275(2), 638-45.
Usowicz MM, et al. Allosteric Interactions at L-type Calcium Channels Between FPL 64176 and the Enantiomers of the Dihydropyridine Bay K 8644. J Pharmacol Exp Ther. 1995;275(2):638-45. PubMed PMID: 7473149.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Allosteric interactions at L-type calcium channels between FPL 64176 and the enantiomers of the dihydropyridine Bay K 8644. AU - Usowicz,M M, AU - Gigg,M, AU - Jones,L M, AU - Cheung,C W, AU - Hartley,S A, PY - 1995/11/1/pubmed PY - 1995/11/1/medline PY - 1995/11/1/entrez SP - 638 EP - 45 JF - The Journal of pharmacology and experimental therapeutics JO - J Pharmacol Exp Ther VL - 275 IS - 2 N2 - Functional interactions between the enantiomers of the dihydropyridine 1,4-dihydro-2,6-dimethyl-5-nitro-4-[2-(trifluoromethyl)-phenyl]-3-pyridi ne carboxylic acid methyl ester (Bay K 8644) and the benzoylpyrrole methyl 2,5-dimethyl-4-[2(phenylmethyl)benzoyl]-H-pyrrole-3-carboxylate (FPL 64176) were investigated on L-type Ca++ channels in guinea pig ileal longitudinal smooth muscle. The effects of these drugs, when applied individually, were as described in earlier studies. For instance, both (-)-(S)-Bay K 8644 and FPL 64176 caused concentration-dependent contraction, which is consistent with Ca++ channel activation, whereas (+)-(R)-Bay K 8644 gave concentration-dependent relaxation, which is consistent with Ca++ channel inhibition. The activities of the different drugs were dependent on the extracellular levels of KCI. When applied in combination, however, the responses evoked were not those predicted from the effects of the drugs applied individually. Contractions produced by FPL 64176 (25 nM to 1 microM) were abolished in the presence of 100 nM (-)-(S)-Bay K 8644 but were potentiated by 10 to 150 nM (+)-(R)-Bay K 8644 and inhibited by 1 microM (+)-(R)-Bay K 8644. Conversely, contractile responses to (-)-(S)-Bay K 8644 were abolished by 100 nM FPL 64176. In the presence of 1 microM FPL 64176, however, (-)-(S)-Bay K 8644 gave concentration-dependent relaxation of the muscle, which is consistent with Ca++ channel inhibition.(ABSTRACT TRUNCATED AT 250 WORDS) SN - 0022-3565 UR - https://www.unboundmedicine.com/medline/citation/7473149/Allosteric_interactions_at_L_type_calcium_channels_between_FPL_64176_and_the_enantiomers_of_the_dihydropyridine_Bay_K_8644_ L2 - https://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=7473149 DB - PRIME DP - Unbound Medicine ER -