Sensitization of the contractile system of canine colonic smooth muscle by agonists and phorbol ester.
- 15 December 1994
- journal article
- Published by Wiley in The Journal of Physiology
- Vol. 481 (3) , 677-688
- https://doi.org/10.1113/jphysiol.1994.sp020473
Abstract
1. Sensitization of the contractile system in response to combinations of excitatory agonists acetylcholine (ACh), methacholine, histamine and neurokinin A (NKA) was investigated in colonic circular smooth muscle of dog, NKA (1 nM) potentiated the contractile response to 1 microM ACh, but did not increase the fura-2 fluorescence ratio (R340/380). Contraction in response to low concentrations of either methacholine or histamine was potentiated significantly by 0.1 microM 4-phorbol 12,13-dibutyrate (PDBu), suggesting that activation of protein kinase C can potentiate contraction at threshold concentrations of agonists. 2. Variability in the sensitivity of the contractile system to Ca2+ was demonstrated over a range of agonist concentrations. KCl, ACh, histamine and NKA each produced a concentration-dependent increase in the amplitude of phasic contractions and R340/380. However, ACh, histamine and NKA each induced maximal increases in R340/380 at concentrations less than that needed to induce maximum force. 3. In depolarized muscles, NKA (50 nM) and PDBu (1 microM) each increased the magnitude of tonic contraction with no change or a decrease in both R340/380 and myosin light chain phosphorylation. In alpha-toxin-permeabilized fibres, 0.1 microM PDBu and 1 microM NKA shifted the Ca(2+)-force response to the left. Ca(2+)-induced contractions were also potentiated by 100 microM GTP-gamma-S or 1 microM NKA plus 10 microM GTP. Potentiation of contraction by NKA and GTP was antagonized by 10 microM GDP-beta-S. 4. The results suggest that endogenous agonists acting via G-proteins sensitize the contractile element of colonic smooth muscle in part by activation of protein kinase C. In some cases, sensitization may be secondary to increased myosin phosphorylation (ACh), but in other cases it appears to be independent of increased myosin light chain phosphorylation (NKA and PDBu). Therefore regulatory mechanisms in addition to myosin phosphorylation contribute to the apparent sensitization of the contractile system to Ca2+.Keywords
This publication has 33 references indexed in Scilit:
- Calponin phosphorylation in vitro and in intact muscleBiochemical Journal, 1993
- Phosphorylation of caldesmon in arterial smooth muscleJournal of Biological Chemistry, 1989
- RECEPTOR-COUPLED PERMEABILIZED SMOOTH-MUSCLE - ROLE OF THE PHOSPHATIDYLINOSITOL CASCADE, G-PROTEINS, AND MODULATION OF THE CONTRACTILE RESPONSE TO CA-2+1989
- Neuropeptide Y augments adrenergic contractions at feline lower esophageal sphincterAmerican Journal of Physiology-Gastrointestinal and Liver Physiology, 1989
- Myoplasmic binding of fura-2 investigated by steady-state fluorescence and absorbance measurementsBiophysical Journal, 1988
- Norepinephrine and GTP-γ-S increase myofilament Ca2+ sensitivity in α-toxin permeabilized arterial smooth muscleBiochemical and Biophysical Research Communications, 1988
- AN ANALYSIS OF AMPLIFYING AND POTENTIATING INTERACTIONS BETWEEN AGONISTS1987
- The effects of phosphorylation of smooth-muscle caldesmonBiochemical Journal, 1987
- Alteration of cytoplasmic ionized calcium levels in smooth muscle by vasodilators in the ferret.The Journal of Physiology, 1984
- CALCULATOR PROGRAMS FOR COMPUTING THE COMPOSITION OF THE SOLUTIONS CONTAINING MULTIPLE METALS AND LIGANDS USED FOR EXPERIMENTS IN SKINNED MUSCLE-CELLS1979