Excitation and contraction of smooth muscle Smooth muscle
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Excitation and contraction of smooth muscle
Smooth muscle Important component of many organ systems: q 1. GI 2. Ureters, uterus 3. Respiratory system - bronchi 4. Blood vessels q Not under voluntary control. q Multiple ways of regulation of activity.
Types of smooth muscle q Multi-Unit q q ciliary muscle and iris muscle of the eye, piloerector muscle Unitary (syncytial or visceral)
Physical structure of smooth muscle Contractile unit similar as in skeletal muscle – but no such regularity. Sidepolar arrangement of myosin heads (in skeletal muscle bipolar) Dense bodies instead of Zdiscs.
Physical structure of smooth muscle Coupling of cells: q 1. dense bodies (physical) 2. gap junctions (electrochemical)
Regulation of contraction by Ca 2+ ions
Smooth muscle cross-bridge cycling q Cross-bridge cycle in smooth muscle is slower than in skeletal muscle. q Due to slower ATP-ase activity of myosin head.
Comparison of smooth muscle to skeletal muscle contraction Slow cycling of myosin bridges (1/10 to 1/100 of skeletal muscle). Fraction of time the cross-bridges remain attached to actin is long low energy requirement for contraction. Slowness of onset of contraction and relaxation (30 x longer than skeletal muscle). Maximum force of contraction greater than skeletal. “Latch” mechanism: sustained muscle contraction with little use of energy.
“Latch” mechanism
“Latch” mechanism
Control systems of smooth muscle
Regulation of contraction Contraction/relaxation can be elicited by: 1. Neural stimuli (autonomic nervous system) 2. Hormones (adrenalin, vasopresin, ACh, angiotensin, oxitocin, histamin) i local factors (p. O 2, p. CO 2, H+) 3. Mechanical stimulus (strech stress relaxation) 4. Spontanous rhythmicity (pacemaker)
Membrane potential and contraction
2+ Ca and contraction
2+ Ca and contraction q Smooth muscle contraction is dependent on extracellular Ca 2+ ion concentration q Cellular entry of extracellular Ca 2+ via: q 1. Opening of voltage-gated Ca 2+ channel (action potential) 2. Opening of ligand-gated Ca 2+ channel (no action potentials) Diffusion of Ca 2+ to all intracellular contractile proteins 50 x longer latent period than in skeletal muscle.
2+ Ca and contraction q Some smooth muscle cells have more developed SR. q Faster contraction after excitation.
- Smooth muscle cells
- Cardiac excitation-contraction coupling
- T tubule
- Acetylcholine binding site
- Muscle contraction
- Autorythmicity
- Sarcoplasmic reticulum
- 3 phases of muscle contraction
- Isotonic vs isometric contraction examples
- Treppe
- Whole muscle contraction
- Incomplete tetanus muscle contraction
- Cross bridge theory
- Muscle
- Isotonic muscle contraction
- Muscle contraction animation mcgraw hill
- Incomplete tetanus muscle contraction