"Excitation-contraction coupling in smooth muscle..."
| Excitation-contraction coupling in smooth muscle is believed to occur by two mechanisms-electromechanical and pharmacomechanical coupling. | |
| Electromechanical coupling operates through changes in surface membrane potential; typically resting membrane potential= -40 to -70 mV. | |
| Primary drive for the rise in intracellular calcium is membrane depolarization, with the consequential opening of voltage operated calcium channels; neurotransmitters or hormones acting to depolarize the membrane will cause contraction while those producing membrane hyperpolarization will cause relaxation. | |
| Like cardiac muscle, the influx of Ca2+ likely causes release of Ca2+ from sarcoplasmic reticulum. | |
"Drugs that block calcium entry..."
| Drugs that block calcium entry through VOCC will inhibit electromechanical coupling-thus the use of calcium channel blocking agents to relax vascular smooth muscle, thus producing vasodilatation and a decrease in blood pressure. | |
| Cell-type dependent; for instance, in asthma, Ca2+ blocking drugs are not effective in promoting relaxation of muscle. | |
| Electromechanical coupling appears to play a predominant role in phasic smooth muscle in which the membrane potential often displays marked oscillations upon which are superimposed calcium spikes | |
| The plasma membranes contain numerous ion channels and the distribution and properties vary among different tissues, contributing to the diversity of smooth muscle. | |