neuromuscular junction steps
Ap spreads across the synaptic knob
AP triggers opening of voltage gated Ca2+ channels
Ca2+ floods into synaptic knob
Ca2+ binds proteins on Ach vesicles
Ach vesicles merge with plasma membrane and Ach is expelled via exocytosis into synaptic cleft
Ach diffuses across the synaptic cleft
Ach Binds receptors on motor end plate (sarcolemma)
Ach receptors are chemically gated, so Ach binding opens the channels
Na+ diffuses into motor end plate and K+ diffuses out (more Na+ diffuses in that K+ moves out)
The flow of ions quickly slows due to resistance, but sufficient to change the RMP from -90mV to -65mV (an end plate potential)
This is enough to trigger opening of voltage gated channels in the sarcolemma to initiate an action potential across the muscle
three types of muscle tissue
skeletal, cardiac, smooth
cardiac muscle
Cardiac, striated, involuntary (not conscious)
smooth muscle
found in walls of hollow visceral organs (stomach, urinary bladder, airways) -visceral, no striated and involuntary
skeletal muscle
Organs attached to bones and skin
Elongated cells called muscle fibers
Striated (striped)
Voluntary (i.e., conscious control)
2 types of protein found in skeletal contraction
actin and myosin
actin
thin filament
myosin
thick filament
muscle functions
Movement of bones or fluids (e.g., blood)
Maintaining posture and body position
Stabilizing joints
Regulating - circular muscle bands called sphincters contract and relax to regulate passage of material - -Generation heat (especially skeletal muscle)
Special Characteristics of Muscle Tissue
Excitability (responsiveness Nervous control): ability to receive and respond to stimuli
Conductivity: can transmit/propagate electrical signals along membranes (action potentials)
Contractility: ability to shorten forcibly when stimulated, unique to muscle cells
Extensibility: ability to be stretched/lengthen
Elasticity: ability to recoil to resting length after stretching
Layers of skeletal muscle
epimysium, perimysium, endomysium
epimysium
dense irregular connective tissue surrounding entire muscle
Perimysium
dense irregular connective tissue surrounding fascicles (groups of muscle fibers)
endomysium
fine areolar connective tissue surrounding each muscle fiber.
Aponeurosis
Broad, sheet-like tendon that fuses muscle to bone, abdominal muscles
flexors
if the center of the connected bones are brought closer together when the muscle contracts (biceps)
extensor
if the bones move away from each other when the muscle contracts Flexor-extensor pairs are called antagonistic muscle groups (triceps)
generate an action potential
Resting state, no ions move through voltage-gated channels
Depolarization caused by massive inflow of Na+
Repolarization is caused by K+ flowing out of the cell
Hyperpolarization caused by continued K+ outflow -hyperpolarization more negative
satellite cells
Cells that do not fuse and remain as single cells in adults (adult stem cells)
myoblasts
stem cells that fuse to form each muscle fiber
Sarcolemma (plasma membrane)
invaginates to form T-tubules extending into sarcoplasmic reticulum
T tubules
tubular infoldings of the sarcolemma which penetrate through the cell and emerge on the other side
sarcoplasm (cytoplasm)
Has typical organelles plus contractile proteins and other specializations
sarcoplasmic reticulum
Surrounds myofibrils like a net sheet
stores calcium •Has pumps that import Ca2+ into sarcoplasmic reticulum where it binds to calmodulin and calsequestrin
•Has channels that allow Ca2+ to be released into surrounding sarcoplasm to trigger contraction
what structures are associated with energy production
-mitochondria -myoglobin -glycogen -creatine phosphate
terminal cisternae
large regions of sarcoplasmic reticulum adjacent to T-tubules and serve as reservoirs for calcium ions and have calcium release channels and calcium pumps (discussed later)
Two cisternae and T-tubule is called a triad -T-tubules contain voltage gated calcium channels
Myoglobin
within cells allows storage of oxygen used for aerobic ATP production
Glycogen
stored for when fuel is needed quickly
creatine phosphate
can quickly give up its phosphate group to help replenish ATP supply
myofibrils
(hundreds to thousands per cell)
Bundles of myofilaments (contractile proteins) enclosed in sarcoplasmic reticulum
Make up most of the cell's volume
myofilaments
contractile proteins bundled in myofibrils
These filaments do not extend the length of the muscle but are found in units - contain thick and thin filaments
I band of sarcomere
regions occupied only by thin filaments
A bands of sarcomere
central region of the sarcomere (thick filament region)
H zone of sarcomere
central region with no thin filament overlap, just thick filaments
M line of sarcomere
thin transverse protein mesh work in center of H zone, an attachment site for thick filaments
sliding filament theory
theory that actin filaments slide toward each other during muscle contraction, while the myosin filaments are still
crossbridge cycling
Crossbridge formation
Power stroke
Release of myosin head
Reset myosin head
rigor mortis
stiffness of the body that sets in several hours after death
no more ATP
Myokinase
transfers Pi from one ADP to another
5 to 6 seconds of max exertion
creatine kinase
transfers Pi from creatine phosphate to ADP
Can 10-15 seconds of energy during max exertion
describe two mechanisms for phosphate transfer
myokinase and creatine kinase
glycolysis
the breakdown of glucose by enzymes, releasing energy and pyruvic acid.
occurs in cytosol
short term supply of ATP
aerobic cellular respiration
the process by which cells use oxygen to obtain usable energy from an energy source
lactic acid
byproduct of anaerobic respiration
oxygen debt
the amount of oxygen required after physical exercise to convert accumulated lactic acid to glucose
what activated action potential in smooth muscle?
stretch
hormones -temperature
glycolitic fibers
use anaerobic cellular respiration
Oxidative fibers (fatigue-resistant)
use aerobic cellular respiration Extensive capillaries Many mitochondria Large supply of myoglobin (red fibers)
Periods of Muscle Contraction
latent period, contraction period, relaxation period
latent period of muscle twitch
Time after stimulus but before contraction begins No change in tension
contraction period of muscle twitch
Time when tension is increasing, if tension becomes great enough to overcome the load, the muscle will shorten
relaxation period of muscle twitch
Time when tension is decreasing to baseline
Begins with release of cross bridges
Ca2+ reentry into SR -Generally, lasts a little longer than contraction period
isometric contraction
no shortening; muscle tension increases but does not exceed load
isotonic contraction
muscle shortens because muscle tension exceeds load
lever
a rigid structure that pivots around a fixed point known as a fulcrum
smooth muscle cells
single, fusiform, uninucleate; no striations
smooth muscle contraction steps
stimulus leads to opening of voltage gated Ca 2+channels
Ca2+ enters sarcoplasm and binds to calmodulin
Calcium-calmodulin complex binds to myosin light-chain kinase (MLCK)
MLCK phosphorylates myosinhead
cross bridges form, pull on actin, similar to skeletal muscle but more slowly
as thin filament slides, it pulls on dense bodies -dense bodies attached to intermediate filaments, which are attached to dense plaques in sarcolemma
these filaments move inward, entire cell shortens
relaxation of smooth muscle contraction
cessation of stimulation
removal of Ca2+ from sarcoplasm
dephosphorylation of myosin by myosin light-chain phosphatase
can be slow to relax due to latch bridge mechanism
fatigue resistant
Energy requirements low compared to skeletal muscle
Can maintain contraction without additional ATP through latch-bridge mechanism
myogenic response
contraction in reaction to stretch, stretch of muscle opens Ca2+ channels
Arteries
carry blood away from the heart
Veins
carry blood to the heart
cardiovascular system
composed of the both heart (pump), blood vessels (tubes) and blood (fluid) To remain healthy, our bodies cells require: • Continuous supply of oxygen and nutrients • Removal of carbon dioxide and wastes
pulmonary circulation
flow of blood from the heart to the lungs and back to the heart
systemic circulation
Transports blood from the left side of the heart to the systemic cells of the body for nutrient and gas exchange - blood brought back to the right side of the heart
Pericardium
Membrane surrounding the heart
fibrous pericardium
dense fibrous irregular connective tissue
parietal pericardium
covers the wall of the pericardial cavity, simple squamous epithelium
visceral pericardium
simple squamous and delicate areolar connective tissue, adheres directly to the heart
epicardium
outermost layer, composed of simple squamous epithelial tissue and an underlining areolar connective tissue
myocardium
composed of a thick layer of cardiac muscle, generates force for contraction
endocardium
internal surface of the heart, simple squamous epithelial tissue and underlying areolar connective tissue
right atrium
three veins drain blood into this chamber, superior and inferior vena cava and the coronary sinus (blood draining from the myocardium) • Separating the right atrium from the right ventricle is the tricuspid valve
deoxygenated blood
right ventricle
deoxygenated blood enters the right ventricle from the atrium and is pumped through the pulmonary semilunar valve into the pulmonary artery - blood is delivered to left and right lungs
left atrium
oxygenated blood moves from the lungs into the left atrium via left and right pulmonary veins • Separating the left atrium from the left ventricle is the bicuspid/mitral valve
left ventricle
blood moves from the left ventricle through the aortic semilunar valve into the aorta and delivers oxygenated blood to the body
divisions of the aorta
-brachiocephalic artery -left common carotid artery
left subclavian artery
brachiocephalic artery
splits into the right subclavian artery and right common carotid artery - supplies right arm, head and neck
left common carotid artery
supplies neck and face
left subclavian artery
supplies left arm, head and thorax
intercalated disks
Cardiac muscle cells are branched and join with their neighbors via junctions
desmosomes
Anchoring junctions that prevent cells from being pulled apart
coronary arteries
run across the surface of the heart and branch extensively
heart conduction system
SA node, AV node, bundle of His, bundle branches, and Purkinje fibers
sinoatrial node
located on the posterior wall of the right atrium, adjacent to the entrance of the superior vena cava. SA node is the pacemaker of the heart
atrioventricular (AV) node
located on the floor of the right atrium
atrioventricular bundle
extends from the AV node into and through the interventricular septum - divides in two
purkinje fibers
extend left and right and continue through the walls of the ventricles
reaching threshold (SA node)
slow leak Na+ channels cause potential to rise, low voltage gated Ca+ channels open, Ca+ flows into nodal cells, RMP -60mV to -40mV
depolarization (SA node)
reaching threshold, causes opening of fast Ca2+ voltage gated channels, Ca2+ enters nodal cell, membrane charge -40mV to just above 0mV
repolarization (SA node)
Ca2+ channels close and voltage gated K+ channels open, K+ flows out of cell, membrane potential returns to -60mV -Process begins again, each process takes about 0.8 sec, results in about 75 beats/min
cardiac conduction system
a system of specialized muscle tissues that conducts electrical impulses that stimulate the heart to beat
found in hearts walls
SA node, AV node, Bundle of HIS, Bundle Branches, perkinje fibers
cardiac muscle cell RMP
-90 mV
SA node RMP
-60 mV
depolarization in cardiac muscle cell
An AP transmitted through the conduction system triggers the opening of fast voltage gated Na+ channels in the sarcolemma, Na+ enters the cell, membrane potential -90mV to +30mV, then voltage gated Na+ channels enter an inactivated state
initial repolarization in cardiac muscle cell
Na+ channels inactivate and K+ leaves through open K+ channels
plateau in cardiac muscle cell
due a decrease in K+ permeability and an increase in Ca2+ permeability. Slow Ca2+ voltage gated channels open, Ca2+ enters the cell, Ca2+ entry causes sarcoplasmic reticulum to release stores of Ca2+ - overall no real change in electrical charge (plateau phase), fast K+ channels close
mechanical events in crossbridge cycling
crossbridge formation
power stroke
release of myosin head
reset of myosin head
muscle relaxation in initiated by closing of voltage gated Ca2+ channels and pumping Ca2+ back into SR or interstitial fluid
crossbridge formation
myosin heads attach to actin
power stroke
myosin head pivots and pulls the thin filament, decreasing sarcomere length