Muscle & Cardiovascular Physiology

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Comprehensive vocabulary flashcards covering skeletal muscle contraction, cross-bridge cycling, mechanics, fiber types, pathology, and complete cardiovascular physiology including cardiac electrophysiology, hemodynamics, and pressure regulation.

45 Terms

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<p>Skeletal Muscle Tissue</p>

Skeletal Muscle Tissue

Striated, multinucleated muscle tissue under voluntary control, featuring cylindrical fibers with peripherally located nuclei and regular transverse banding patterns.

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<p>Cardiac Muscle Tissue</p>

Cardiac Muscle Tissue

Striated, involuntary muscle tissue found exclusively in the heart wall, characterized by branching fibers, single central nuclei, and intercalated discs connecting adjacent cardiomyocytes.

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<p>Smooth Muscle Tissue</p>

Smooth Muscle Tissue

Non-striated, involuntary muscle tissue composed of spindle-shaped cells with a single centrally located nucleus, found in the walls of hollow organs and blood vessels.

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Sarcomere

The repeating functional unit of muscle contraction and shortening, delimited by two Z-lines, consisting of aligned thick (myosin) and thin (actin) myofilaments.

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Tropomyosin

A thread-like regulatory protein that lies along the groove of actin filaments and physically blocks cross-bridge binding sites on actin when cytosolic Ca2+Ca^{2+} is low.

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Troponin

A three-subunit regulatory protein complex bound to actin and tropomyosin that binds cytosolic Ca2+Ca^{2+}, undergoing a conformational shift that pulls tropomyosin off the myosin-binding sites.

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DHP Receptor (Dihydropyridine Receptor)

A voltage-sensing protein embedded in the transverse tubule (T-tubule) membrane that changes conformation in response to action potentials to open adjacent ryanodine receptor channels.

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Ryanodine Receptor

A calcium-release channel situated in the terminal cisternae membrane of the sarcoplasmic reticulum that releases stored Ca2+Ca^{2+} into the cytosol upon activation by DHP receptors.

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SERCA Pump

A Ca2+Ca^{2+}-ATPase transporter located in the sarcoplasmic reticulum membrane that actively pumps cytosolic Ca2+Ca^{2+} back into the sarcoplasmic reticulum lumen using ATP, inducing muscle relaxation.

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Cross-Bridge Cycle

The four-step molecular mechanism of muscle contraction wherein energized myosin binds actin, executes a power stroke upon releasing ADPADP and PiP_i, unbinds upon binding a new ATPATP, and re-energizes via ATP hydrolysis.

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Rigor Mortis

The state of persistent muscle rigidity that occurs after death due to ATP depletion, preventing ATP from binding myosin to break the cross-bridge linkage with actin.

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Motor Unit

A single somatic motor neuron and all of the individual skeletal muscle fibers that it innervates, which contract in an all-or-none fashion when stimulated.

<p>A single somatic motor neuron and all of the individual skeletal muscle fibers that it innervates, which contract in an all-or-none fashion when stimulated.</p>
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<p>Muscle Tetanus</p>

Muscle Tetanus

A sustained, maximal muscle contraction resulting from repetitive, high-frequency stimulation; it presents as unfused tetanus when stimuli occur during partial relaxation, and fused tetanus when stimuli arrive before any relaxation occurs.

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Physiological Cross-Sectional Area (PCSA)

A structural parameter of muscle architecture reflecting the total number of sarcomeres aligned in parallel, which is directly proportional to maximum active tension production.

<p>A structural parameter of muscle architecture reflecting the total number of sarcomeres aligned in parallel, which is directly proportional to maximum active tension production.</p>
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Creatine Phosphate

A high-energy phosphate molecule that rapidly regenerates ATPATP from ADPADP via the enzyme creatine kinase during the initial seconds of muscle activity (CP+ADP⇌C+ATPCP + ADP \rightleftharpoons C + ATP).

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Slow-Oxidative Fibers (Type 1)

Fatigue-resistant skeletal muscle fibers characterized by high myoglobin content, abundant mitochondria, low myosin-ATPase activity, and slow contraction velocity, recruited first during movement.

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Fast-Glycolytic Fibers (Type 2X)

Easily fatigable skeletal muscle fibers characterized by high glycolytic enzyme activity, low myoglobin content, high myosin-ATPase activity, and fast contraction velocities, organized into large motor units for burst power.

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Duchenne Muscular Dystrophy (DMD)

An X-linked recessive genetic disorder caused by mutations preventing the production of functional dystrophin, leading to progressive muscle cell membrane instability, damage, and severe muscle wasting.

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<p>Gowers' Sign</p>

Gowers' Sign

A clinical sign of proximal muscle weakness wherein a patient uses their hands and arms to physically 'walk up' their lower limbs in order to stand from a supine or seated floor position.

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<p>Hematocrit</p>

Hematocrit

The fraction of total whole blood volume occupied by packed erythrocytes following centrifugation, normally approximating 45%45\%.

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Erythropoietin (EPO)

A peptide hormone produced primarily by the kidneys that stimulates the proliferation and differentiation of erythrocyte progenitor cells in the bone marrow.

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Intercalated Discs

Specialized transverse junctions connecting adjacent cardiac muscle cells end-to-end, containing desmosomes for structural anchoring and gap junctions for electrical coupling.

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Contractile Cardiomyocyte Plateau Phase (Phase 2)

The sustained depolarization phase of a ventricular action potential produced by an influx of Ca2+Ca^{2+} through voltage-gated L-type Ca2+Ca^{2+} channels balanced by an efflux of K+K^+.

<p>The sustained depolarization phase of a ventricular action potential produced by an influx of $$Ca^{2+}$$ through voltage-gated L-type $$Ca^{2+}$$ channels balanced by an efflux of $$K^+$$.</p>
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Cardiac Refractory Period

A prolonged period lasting approximately 250 ms250\,\text{ms} during which a contractile cardiomyocyte cannot be re-excited, preventing tetanus and allowing rhythmic chamber relaxation and ventricular filling.

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Pacemaker Potential

The spontaneous, slow diastolic depolarization (∼−60 mV\sim -60\,\text{mV} to −40 mV-40\,\text{mV}) of autorhythmic cardiac cells driven by inward Na+Na^+ via F-type channels, inward Ca2+Ca^{2+} via T-type channels, and declining outward K+K^+ current.

<p>The spontaneous, slow diastolic depolarization ($$\sim -60\,\text{mV}$$ to $$-40\,\text{mV}$$) of autorhythmic cardiac cells driven by inward $$Na^+$$ via F-type channels, inward $$Ca^{2+}$$ via T-type channels, and declining outward $$K^+$$ current.</p>
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Sinoatrial (SA) Node

A specialized collection of autorhythmic pacemaker cells in the right atrial wall near the superior vena cava that sets the intrinsic resting heart rhythm at approximately 70 action potentials per minute70\,\text{action potentials per minute}.

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<p>Electrocardiogram (ECG)</p>

Electrocardiogram (ECG)

A non-invasive clinical tracing of electrical potential differences recorded at the body surface, reflecting the summation of all electrical dipole currents generated by cardiac action potentials.

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P Wave

The initial deflection on an electrocardiogram tracing that represents the spread of electrical depolarization through the atria.

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QRS Complex

The prominent electrocardiographic waveform representing ventricular depolarization, during which atrial repolarization also occurs simultaneously.

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T Wave

The electrocardiographic wave representing the repolarization of the ventricles.

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<p>Heart Murmur</p>

Heart Murmur

An abnormal sound heard over the heart produced by turbulent blood flow, resulting either from a stenotic valve that fails to open fully or an insufficient valve that permits backward leakage.

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Isovolumetric Ventricular Contraction

The early phase of ventricular systole in which ventricles contract with all valves closed, causing ventricular pressure to spike rapidly without changes in ventricular blood volume.

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Stroke Volume (SV)

The volume of blood pumped out by each ventricle with a single heartbeat, defined as end-diastolic volume minus end-systolic volume (SV=EDV−ESVSV = EDV - ESV).

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Cardiac Output (CO)

The total volume of blood pumped out by each ventricle per unit time, calculated as the product of heart rate and stroke volume (CO=HR×SVCO = HR \times SV).

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Ejection Fraction (EF)

The percentage of end-diastolic blood volume ejected from a ventricle during a single beat, defined as EF=SVEDVEF = \frac{SV}{EDV}, used clinically to assess cardiac contractility.

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Preload

The degree of stretch exerted on ventricular cardiomyocytes at the end of diastole, determined by end-diastolic volume (EDV) and operating through the Frank-Starling mechanism to increase stroke volume.

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Afterload

The combined arterial pressure and vascular resistance that the ventricles must overcome to open the semilunar valves and eject blood.

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Inotropy

The intrinsic contractility of cardiac muscle cells at any given end-diastolic volume, augmented extrinsically by sympathetic stimulation of β1\beta_1-adrenergic receptors via cAMP and protein kinase A.

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Elastic Arteries

Thick-walled, large-diameter conduit vessels located close to the heart (such as the aorta) that distend during ventricular ejection and recoil during diastole to act as pressure reservoirs.

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Mean Arterial Pressure (MAP)

The average pressure driving blood through the systemic capillary beds, calculated as diastolic pressure plus one-third pulse pressure (MAP=DP+13×PPMAP = DP + \frac{1}{3} \times PP) or as MAP=CO×TPRMAP = CO \times TPR.

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Pulse Pressure (PP)

The difference between systolic pressure and diastolic pressure (PP=SP−DPPP = SP - DP), reflecting stroke volume and arterial compliance.

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Active Hyperemia

An intrinsic local regulatory response where elevated tissue metabolic rate causes local decrease in O2O_2 and accumulation of metabolites, triggering arteriolar vasodilation and increased organ blood flow.

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Capillary Bulk Flow

The passive, non-diffusional volume filtration and absorption of protein-free plasma across capillary walls driven by the balance of hydrostatic and colloid osmotic Starling pressures.

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Skeletal Muscle Pump

A peripheral circulatory mechanism where contracting skeletal muscles compress deep veins, elevating venous pressure and driving blood through one-way venous valves toward the heart.

<p>A peripheral circulatory mechanism where contracting skeletal muscles compress deep veins, elevating venous pressure and driving blood through one-way venous valves toward the heart.</p>
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<p>Arterial Baroreceptors</p>

Arterial Baroreceptors

Sensory stretch receptors situated in the carotid sinuses and aortic arch that monitor systemic blood pressure and adjust afferent firing rates to the medullary cardiovascular control center.