Epinephrine takes a longer time to act on the heart than sympathetic stimulation does, but the effect lasts longer.
The pericardium is a sac that surrounds the heart and consists of the fibrous pericardium and the serous pericardium.
The fibrous pericardium helps hold the heart in place.
The serous pericardium reduces friction as the heart beats.
The parietal pericardium lines the fibrous pericardium.
The visceral pericardium lines the exterior surface of the heart.
The pericardial cavity lies between the parietal and visceral pericardia and is filled with pericardial fluid, which reduces friction as the heart beats.
The heart wall has three layers: the outer epicardium (visceral pericardium), the middle myocardium, and the inner endocardium.
The inner surfaces of the atria are mainly smooth.
The auricles have muscular ridges called pectinate muscles.
The ventricles have ridges called trabeculae carneae.
Each atrium has a flap called an auricle.
The coronary sulcus separates the atria from the ventricles.
The inter-ventricular grooves separate the right and left ventricles.
The inferior and superior venae cavae and the coronary sinus enter the right atrium.
The four pulmonary veins enter the left atrium.
The pulmonary trunk exits the right ventricle, and the aorta exits the left ventricle.
Coronary arteries branch off the aorta to supply the heart.
Blood returns from the heart tissues to the right atrium through the coronary sinus and cardiac veins.
The interatrial septum separates the atria from each other, and the interventricular septum separates the ventricles.
The tricuspid valve separates the right atrium and ventricle.
The bicuspid valve separates the left atrium and ventricle.
The chordae tendineae attach the papillary muscles to the atrioventricular valves.
The semilunar valves separate the aorta and pulmonary trunk from the ventricles.
Cardiac muscle cells are branched and have a centrally located nucleus.
Actin and myosin are organized to form sarcomeres in cardiac muscle cells.
The sarcoplasmic reticulum and T tubules are not as organized as in skeletal muscle in cardiac muscle cells.
Cardiac muscle cells are joined by intercalated disks, which allow action potentials to move from one cell to the next.
Parasympathetic stimulation has an inhibitory influence on the heart, primarily by decreasing the heart rate.
The heart's pumping effectiveness is greatly influenced by relatively small changes in the preload, but it is very insensitive to large changes in afterload.
The Starling law of the heart describes the relationship between changes in the pumping effectiveness of the heart and changes in preload.
During exercise, skeletal muscle activity greatly influences heart activity by altering venous return and preload.
During exercise, blood vessels in exercising skeletal muscles dilate and allow more blood to flow through the vessels, increasing O, and nutrient delivery to the exercising muscles.
Skeletal muscle contractions repeatedly compress veins and cause blood to flow more rapidly from the skeletal muscles toward the heart, increasing venous return to the heart and increasing the preload.
If venous return remains constant while the heart is inhibited by parasympathetic stimulation, stroke volume can actually increase.
Afterload is the pressure the contracting left ventricle must produce to overcome the pressure in the aorta and move blood into the aorta.
The increase in stroke volume results in increased cardiac output, and the volume of blood flowing to the exercising muscles increases.
The increased preload causes an increased force of cardiac muscle contraction, which increases stroke volume.
Aortic blood pressure must increase to more than 170 mm Hg before it hampers the ventricles' ability to.
Strong parasympathetic stimulation can decrease the heart rate below resting levels by at least 20-30 bpm, but it has little effect on stroke volume.