Cardiovascular and Respiratory Systems Flashcards

1
Q

describe the pericardium (3)

A
  • 2 layers of serous pericardium: visceral (attached to heart) and parietal (attached to fibrous peri.)
  • fibrous pericardium attaches to surrounding structures (eg. diaphragm)
  • pericardial space between serous layers to lubricate and decrease friction when the heart contracts within the pericardium
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2
Q

describe the epicardium (2)

A
  • thin layer of connective tissue on the outside of the heart
  • contains adipose tissue, nerves and coronary vessels
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3
Q

describe the myocardium

A

thickest layer of heart tissue made up of cardiac muscle cells

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4
Q

describe the layers of the endocardium (3)

A
  • outer nerves, veins and Purkinje fibres
  • middle connective tissue
  • inner endothelium
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5
Q

describe the composition of heart valves (3)

A
  • continuous with cardiac wall
  • collagenous layer toughens to become highly fibrous
  • avascular (vulnerable to endocarditis)
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6
Q

describe the fibrous heart skeleton (4)

A
  • fibrocollagenous rings of connective tissue
  • surround aorta, pulmonary trunk and AV openings
  • where valves and cardiac muscle attaches
  • electrically insulates atria from the ventricles
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7
Q

describe the intercalated discs at the branch points of cardiac myocytes (3)

A
  • desmosomes - proteoglycan bridges between cells, preventing separation of cells during contraction
  • gap junctions - permit electrical conductivity
  • adherens - anchoring sites for actin
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8
Q

what is the 2 main difference between pacemaker cells and normal cardiac myocytes?

A
  • pacemaker cells are specialised cardiac myocytes with no myofibrils, so they cannot contract
  • have different transmembrane proteins which allow them to spontaneously trigger action potentials
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9
Q

describe the structure and function of the tunica intima of (3)

A
  • single layer of endothelial cells - BP control, prevention of platelet aggregation, angiogenesis and act as a permeability barrier between plasma and interstitial fluid
  • endothelial tight junctions prevent movement of blood cells and large proteins out of blood
  • surrounded by internal elastic lamina - separates from tunica media
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10
Q

describe the structure and function of the tunica media of BVs (3)

A
  • smooth muscle cells arranged in circular and spiral layers, supported by elastic fibres and collagen
  • sympathetic innervation - vasoconstrictor tone (arterial blood pressure and compliance of systemic veins)
  • surrounded by external elastic lamina - thick elastic tissue, separates from tunica externa
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11
Q

describe the main features of hypertrophic cardiomyopathy (4)

A
  • myocardial hypertrophy (thickened wall due to enlarged cells)
  • defective diastolic filling
  • in 1/3, ventricular flow obstruction
  • systolic function preserved, by myocardium cannot properly relax
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12
Q

describe the pathogenesis of hypertrophic cardiomyopathy (5)

A
  • mutation to genes of contractile structures
  • affect sarcometric proteins to increase myofilament function
  • myocytes hyper contractility and increased energy use
  • hypertrophy in response to stress
  • often disproportionate thickening of ventricular septum (asymmetric septal hypertrophy)
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13
Q

how can hypertrophic cardiomyopathy result in functional LV outflow tract obstruction? (3)

A
  • septal hypertrophy - septum is particularly thickened
  • contact of thickened septum with mitral valve
  • causes thickening of a mitral leaflet
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14
Q

describe the common symptoms of hypertrophic cardiomyopathy (often asymptomatic / mild symptoms) (4)

A
  • dypnoea - reduced LV diastolic function, can result in pulmonary oedema
  • syncope / presyncope - due to inadequate cardiac output or arrhythmias (can cause sudden cardiac death)
  • chest pain - micro vascular complications or deficit in O2 demand of myocardium, and perfusion of coronary arteries (impaired diastolic function)
  • palpitations - arrhythmias
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15
Q

what is the inheritance pattern of hypertrophic cardiomyopathy in most cases?

A

autosomal dominant - if one parent has one faulty gene, 1/2 chance of the condition being inherited by offspring (non-sex chromosome)

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