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cardiac function in body
pump blood, maintain BP, supply oxygen and nutrients to body, remove CO2 and waste from body
skeletal muscle is what type of syncytium
true syncytium
cardiac muscle is what type of syncytium
functional syncytium
similar to skeletal muscle, cardiac muscles are
striated muscles
striated muscles contract in the absence of
nerve activity (involuntary)
what is a function unit of cardiac muscles called
sarcomere
are fibers branched?
yes
how do fibers connect one another at the cardiomyocycte cell membrane
by intercalated discs
intercalated discs contain what that allows free diffusion of ions
several permeable gap junctions
why do ions move easily in intracellular fluid along longitudinal axes of cardiac muscle fibers
so action potential travel easily from one cardiac muscle cell to the next
cardiac muscle is a _________ of many heart muscle cells
syncytium
what does the cardiac muscle being a syncytium contribute to
allows action potential to spread to all heart muscle cells
where are the nuclei in cardiac muscle cells
centrally located
where are cardiac muscle cells nuclei abundant
mitochondria
sarcolemma has what kind of specialized ion channel
voltage gated Ca channel
SR less abundant than _____ muscle, but greater density than ______muscle
skeletal, smooth
what is a key feature of cardiac myocyte
intercalated disk
what is the intercalated disk composed of
adherens junction, desmosome, gap junctions
types of adherens junctions
C, alpha, beta, gamma, delta
Cadherins
family of transmembrane protein that form homodimer in Ca-dependent manner with other cadherin molecule on adjacent cell
delta-catenin
bind juxtamembrane region of cadherin
gamma-catenin
bind catenin bind region of cadherin
beta-catenin
bind cytoplasmic region of cadherin
alpha-catenin
link actin cytoskeleton to N-cadherins by binding to beta or gamma catenin
desmosomes
composed of desmosome intermediate filament complexes (DIFC)
DIFC
network of cadherin proteins, linker protein, and intermediate filaments
DIFC can be broken into 3 regions
ICS, ODP, IDP
what does extracellular core gion contain
desmoglein and desmocollin
desmoglein and desmocollin are both
cadherin family of cell adhesion proteins, have 4 extracellular domains and have Ca binding motifs
what contributes to ODP region of desmosome
plakophillin, plakoglobin, N-terminus globular domain of desmoplakin
what contribtues to IDP region of desmosome
C-terminus globular domain of desmoplakin and intermediate filament interaction region
gap junction
specialized intracellular connections that directly connect cytoplasmm of 2 cells and allow various things to pass directly through regulated gate between cells
what is 1 gap junction channel composed of
2 protein hexamers called connexons, which connect across intracellular space bridging gap between 2 cells
adherens junction overall
connects actin filaments of adjoining cardiomyocytes
desmosome overall
connects to intermediate filaments of adjoining cardiomyocytes
gap junctions overall
opening to allow flow of ions, action potential, molecules, between cardiomyocytes
2 specialized cardiac muscle cells
contractile and autorhythmic
contractile cells
99% of cardiac muscle cells, do mechanical work of pumping
autorhythmic cells
dont contract, intiiate and conduct AP responsible for contraction of working cells
electrophysiological properties of cardiac muscles
automaticity, excitabilty, conductivity, contractiliy, rhtyhmicity
automaticity
abilty to spontaneously generate electrical impulse
excitability
ability to respond to an electrical impulse
conductivity
allow transmission of electrical impulse to another cardiac cell
contractility
ability to contract after electrical impulse response
rhythmicity
ability to send electrical impulses in regular manner
excitation of heart triggered by
electrical impulse rather than neural transmitters
contraction of heart triggered by
elevation of intracellular calcium influx
reason for plateau in AP for cardiac muscle and NOT skeletal muscle
-L type Ca channel slower to open and stay open longer
-permeability of cardiac muscle membrane for K ions decreases by 5 fold
in phase 0 of cardiac AP (depolarization)
influx of Na, voltage gated ion channel open
in phase 1 of cardiac AP (inital repolarization)
Na channel close
in phase 2 of cardiac AP (plateau)
slow Ca channel open
in phase 3 of cardiac AP (rapid repolarization)
slow Ca channel close
in phase 4 of cardiac AP (resting membrane potential)
K channel close
energy for cardiac contraction
derived from catabolism of fatty acids, glucose, lactate, and ketone bodies
after fatty meal
60% from oxidation of fatty acids
starvation
breakdown of adipose tissue (ketone bodies)
cardiac performance is function of
preload, afterload, contractility, heart rate
preload
myocardial stretch at end of diastole
afterload
resistance ventricle must overcome to eject blood
heart rate
# of times heart beat in minute
rank of cardiac output in autonomic nervous system control from high to low
maximum sympathetic, normal sympathetic, zero sympathetic, parasympathetic
when end diastolic volume (EDV) increases
stretches muscle fibers, force of contraction and output per beat (SV) increase up to limit, beyond which stroke volume falls with further increase in diastolic volume
end diastolic volume (EDV)
volume of blood in left ventricle at end of ventricular filling
stroke volume (SV)
volume of blood pumped out of left ventricle of heart during each systolic cardiac contraction
cardiac output (CO)
heart rate x SV
ejection fraction (EF)
SV/EDV x 100%
regulation of heart pumping
frank sterling mechanism and autonomic nervous system
frank sterling mechanism
intrinsic cardiac regulation of pump in response to change in volume of blood flowing into heart
autonomic nervous system
control of heart rate and strength of heart pumping by parasympathic and sympathetic nerves
at rest heart pump
4-6 liter per minute
during exercise heart pump
12-35 liter per minute
how does sinoatraial node cell generate impulse for cardiac contraction for life (loop)
self excite to cause AP → recovery from AP→ hyperpolarization after AP is over → drift of resting potential to threshold (loops)
how does sinoatraial node cell generate impulse for cardiac contraction for life (step)
-high Na conc in ECF and leaky Na channel lets Na into cell
-threshold reached, L type Ca channel opens (depolarization)
-Ca channel close within 100-150 millisecond after opening
-K channel open
-K channel close, leakiness of Na channel restarts cycle

PQRST and AP trace (how it works)
if electrode place on opposite side of heart on skin, electrical potential generated by current can be recorded by electrocardiogram (ECG)
AV node impulse delay ensures
the atria empties their blood into ventricles before ventricular contraction begins
cardiac electrical activity coordinates
pumping action of the heart

P wave
atrial depolarization

QRS complex
ventricular depolarization

ST-T segment
ventricular repolarization
excitation-contraction coupling and relaxation in cardiac muscle
-AP open Ca channel in t-tubule (5x wider than skeletal)
-rely in Ca from extracellular space for contraction (95% stored in cells)
-contraction similar to skeletal muscle, Ca dependent
-SR Ca pump and Ca-Na exchanger remove Ca during relaxation
-Na transported out of cell by Na-K pump to reach resting potential
in skeletal muscle ____% of Ca is stored in t-tubule and SR
100
where do we see a plateau, in the skeletal or cardiac muscle
cardiac muscle
summary of excitation-contraction coupling in cardiac contractile cells
-Ca enter cell (depolarization) trigger release of Ca by terminal cisternae
-Ca bind to troponin C induce conformation change in troponin complex
-myosin head bind to actin, cross bridge movement (ATP hydrolysis needed) and reduction in sarcomere length
-Ca resequestered by SR by SERCA pump
-Ca removed from troponin C and myosin unbind from actin (ATP needed), allows sarcomere to resume original relaxed length