2Smooth Muscle AnatomySmooth muscle is considered to be much more primitive than either cardiac or skeletal muscle. Muscle striations are not visible in smooth muscle, so the sarcomere relationship of myosin to actin does not exists in smooth muscle. However, per cross sectional area smooth muscle is as strong as skeletal muscle and smooth muscle is highly resistant to fatigue.
3Smooth Muscle Anatomy I. Smooth Muscle 1. Fibers are smaller than skeletal muscle2. Involuntary (Usually)3. No apparent myofibrils under the light microscope - No cross striations4. Fibers are thickest in the middle and have tapered ends5. Centrally located single oval nucleus
5Smooth Muscle Anatomy 6. Sarcoplasm contains thick and thin filaments a. Not in an orderly patternb. 10 – 20 times more thin filaments than thick filaments7. Dense bodiesa. Have thin filaments attached to themb. Function is similar to Z disksc. Dispersed throughout the sarcoplasm or attached to the sarcolemmad. Thin filaments stretch from one dense body to another
7Smooth Muscle Anatomy B. Generation of Contraction 1. Sliding filament mechanism involving thick and thin filaments generates tension that is transmitted to the thin filaments2. Does not contain Troponin complex3. Actin and myosin pull on the dense bodies attached to the sarcolemma4. Shortening of the smooth muscle fiber is lengthwise, the middle of the fiber thickens
9Smooth Muscle Anatomy5. Shortening causes bubble like expansion of the sarcolemma6. Shortening is corkscrew like - the fiber twists in a helix as it shortens and rotates in the opposite direction as it lengthens
10Smooth Muscle Anatomy Structure of Smooth Muscle II. Types of Smooth Muscle - Single unit and multi unitSize - Smooth muscle is much smaller than either skeletal or cardiac muscleOrganization into bundles or sheets (Single unit)Response to different types of stimuliNerves, hormones, mechanical stretch, endothelial mediators (EDNO)
11Smooth Muscle Anatomy Structure of Smooth Muscle Characteristics of innervation - Innervated by ANS - Swellings along the Axon are synapses - Continuous firing the firing rate determines the concentration of neurotransmitter, hence the degree of physiological responseFunction - Control the size of organs - cause the release of substances - Control the rate of flow (blood, contents of GI tract, urine) - etc.
12Smooth Muscle Anatomy Structure of Smooth Muscle Types of smooth muscles -Single Unit - Large aggregates of smooth muscle cells which act as a single unit.Multi Unit - Single smooth muscle cells usually with a single nerve connection
13Smooth Muscle Anatomy Structure of Smooth Muscle Multi Unit - Single smooth muscle cells usually with a single nerve connection Examples - Arrector pili muscles, Vas deferens and iris of the eye.
14Smooth Muscle Anatomy Structure of Smooth Muscle A. Multi-unit smooth muscle1. Individual fibers - independent of all other fibers2. Fibers contain their own motor neuron terminals with few gap junctions and control is mostly nervous3. Covered by a thin layer of basement membrane of fine collagen and glycoprotein fibrillae that help to insulate the fiber
15Smooth Muscle Anatomy Structure of Smooth Muscle 4. Action potential causes the stimulation of one single muscle fiber5. Seldom exhibit spontaneous contractions6. Found in:a. Walls of large arteriesb. Airways of lungs (Bronchioles)c. Arrector pili muscles attached to hair folliclesd. Radial and circular muscles of the iris of the eye
16Smooth Muscle Anatomy Structure of Smooth Muscle Single Unit - Large aggregates of smooth muscle cells which act as a single unit.. These usually line the hollow organs such as blood vessels or the gastrointestinal tract.
17Smooth Muscle Anatomy Structure of Smooth Muscle Single Unit - Unitary Smooth Muscle - (Syncytial smooth muscle or visceral smooth muscle)1. Most common - sheets or bundles of large numbers of smooth muscle fibers that act as if they were a single unit (Syncytium)2. Cell membranes adhere to multiple points and gap junctions join cells (electrical continuity)
18Smooth Muscle Anatomy Structure of Smooth Muscle 3. Location;a. Form part of the walls of both large and small arteries and veinsb. Hollow viscera - Stomach, intestines, uterus, urinary bladder4. Muscle forms large networks and an action potential causes contraction of the entire organ
19Smooth Muscle Contractile Mechanism C. Contractive Process in Smooth Muscle1. Chemical basis for smooth muscle contractiona. Contains actin and myosin filaments similar in structure and interaction to skeletal muscleb. No troponin complex - mechanism for contraction is differentc. Calcium influx activates the contractile processd. ATP provides energy for contraction
20Smooth Muscle Contractile Mechanism E. Major differences between smooth muscle and skeletal musclePhysical organization of smooth muscleExcitation-contraction-couplingControl of the contraction process by calciumDuration of contractionAmount of energy required for contraction2. Physical basis for smooth muscle contraction
21Smooth Muscle Contractile Mechanism A. Smooth muscle is not striatedb. Dense bodies - attachment for actin fibers - some attach to cell membrane others located throughout the cytoplasm - dense bodies in one cell may join with a dense body in the adjacent cellc. Few myosin fibers are located in the actin fibers (15:1 ratio of actin to myosin)
23Smooth Muscle Contractile Mechanism 3. Comparison of smooth muscle contraction with skeletal muscle contractiona. Starts slower and lasts longer than striated muscle fiber, smooth muscle has a prolonged contraction - up to hours to daysb. Can shorten and stretch to a greater extent than striated musclec. Contraction is initiated by calcium influx into the sarcoplasm (Outside Calcium)
24Smooth Muscle Contractile Mechanism D. Sarcoplasmic reticulum in smooth muscle is sparse - 3 to 5 % of cell volumee. Calcium flows into sarcoplasm from extracellular fluidf. No T-tubules in smooth muscle - Therefore, calcium movement is slowg. Smooth muscle tone - occurs due to the slow movement of calcium from the cellh. Smooth muscle has less ATPase activity and therefore, less degradation of ATP
25Smooth Muscle Contractile Mechanism I. Smooth muscle only needs 1/10 to 1/300 of the energy that skeletal muscle requiresj. Only one ATP is required per contraction cycle no matter how long it lastsk. Smooth muscle reaches full contraction about 1/2 second after stimulationl. Contractile force reaches maximum within seconds after stimulation
26Smooth Muscle Contractile Mechanism M. Rate of contraction is 30 times slower than skeletal musclen. Contractions can last from 0.2 to 30 secondso. Smooth muscle force of contraction can be approximately 2X that of skeletal musclep. Smooth muscle can shorten to a greater degree than skeletal muscle reduces lumen of organs to almost zero
27Smooth Muscle Contractile Mechanism 4. “Latch Mechanism - prolonged holding in smooth musclea. After contraction is initiated, less stimulus and energy are needed to maintain the contraction (Energy conservation)b. Can maintain prolonged tonic contractions for hours with little energy and little excitatory signal from nerves or hormones
28Smooth Muscle Contractile Mechanism C. Mechanism: lower activation of enzymes, myosin head remains attached to actin for long periods of time but large numbers are attached and the force is great5. Stress - Relaxation of Smooth MuscleImportant characteristic of visceral smooth muscle
29Smooth Muscle Contractile Mechanism Stress - Relaxation response - ability to return nearly to the original force of contraction seconds to minutes after it has been elongated or shorteneda. When smooth muscle is initially stretched - it will contract and increase tension (Myogenic response)b. Smooth muscle fibers can stretch and still maintain their contractile function
30Smooth Muscle Contractile Mechanism C. Smooth muscle can undergo great changes in length and still retain the ability to contract effectivelyd. This response allows vessels and hollow organs to change size but maintain the pressure within the structure at a constant level (Probably related to the “latch mechanism”)
31Smooth Muscle Contractile Mechanism D. Regulation of Contraction by Calcium Ionsa. ICF calcium is the initiating event for smooth muscle contractionb. An increase in calcium influx can be caused by: nerve stimulation, hormones, chemical changes in the environment (Ligands), and mechanical stretch of the fiber
32Smooth Muscle Contractile Mechanism 2. Role of calmodulin in excitation-contraction-coupling in smooth musclea. Smooth muscle has no Troponin but it does have a regulatory protein called calmodulinb. Calmodulin is similar in structure to Troponin and like Troponin combines with 4 calcium ions causing activationc. Activated calmodulin-Ca++ complex activates myosin light chain kinase
34Smooth Muscle Contractile Mechanism d. The activated myosin light chain kinase phosphorylates the myosin light chains (regulatory proteins on the myosin heads) using an ATP unite. The myosin heads now engage actin and cross bridge cycling proceeds using the same process as in skeletal musclef. Cessation of contraction1. As [Ca++] drops below a critical level2. Myosin phosphatase removes the phosphate from the myosin light chains and contraction stops
36Smooth Muscle Contractile Mechanism Regulation of the myosin light chain and smooth muscle contraction -While the MLCK adds a P group to the MLC dependent on [Ca++] myosin light chain phosphatase removes it deactivating the myosin head. The phosphatase is continually active.
37SMOOTH MUSCLE STIMULATION Smooth muscle responds to stimulation from a number of different physiological systems.1. Nerves2. Hormones3. Mechanical manipulation4. Self stimulation (Automaticity)
39SMOOTH MUSCLE STIMULATION 2. Excitatory and inhibitory transmitter substances at NMJa. Ach & norepinephrine are never secreted by the same nerve fiberb. Ach can be excitatory or inhibitory - determined by the type of receptor expressed by the target cellc. Ach and NE usually cause the opposite reaction at a target cell (If Ach is stimulatory then NE will most likely be inhibitory)
40SMOOTH MUSCLE STIMULATION Unitary B. Membrane Potential and AP in smooth muscle (Slow waves and Spike Potentials)1. Unitary smooth musclea. Slow waves - In smooth muscle the resting membrane potential is variable - usually about -50 to -60 mVb. Variable resting membrane potential is called the basic electrical rhythm or BER or sometimes slow waves
42SMOOTH MUSCLE STIMULATION Unitary B. Slow waves and spontaneous generation of action potentials1. Slow waves are not action potentials - they are local unstable resting membrane potential and they determine the rhythmicity of smooth muscle contractions2. Slow waves can initiate true action potentials called spike potentials (Ca++ voltage gated)3. Spike potentials are generated whenever BER exceeds threshold about -35 mV
43SMOOTH MUSCLE STIMULATION Unitary Spike Potentialsa) Spike potentials cause rhythmic contractions of smooth muscleb) Increase the number of spike potentials and increase the force of smooth muscle contractionc) Regulation - mechanical stretch, hormones, and Ach cause membrane to become less negative (Hypopolarize the cells)
45Depolarization of Multiunit Smooth Muscle w/o AP Smooth muscle contraction in response to local tissue factors1) Arterioles, metarterioles & precapillary sphincters have little or no nerve supply2) Highly contractile smooth muscle responds rapidly to local factorsLack or a decrease in O2 levels - Increase in CO2 - Increase in hydrogen ions - Decrease in ECF Ca++ - Adenosine or increased lactic acid – Cause Vasodilation
46Depolarization of Multiunit Smooth Muscle w/o AP C. Effect of hormones on smooth muscle contraction1) Most hormones affect smooth muscle through second messengers2) Important hormones - Norepinephrine, epinephrine, Ach, angiotensin II, oxytocin, vasopressin, serotonin and histamine3) Action of hormones is controlled by the type of receptors expressed by the target cell - hormone (Ligand) gated excitatory and inhibitory receptors (Ca++ or K+ channels)
47Smooth MuscleSUMMARY1. How does smooth muscle differ from skeletal muscle?2. How is excitation contraction coupling control different in smooth muscle from skeletal muscle?3. What are slow waves or BER and spike potentials?4. How is BER controlled?