By David Mohrman, Lois Heller

The research consultant that enables you to actually comprehend instead of purely memorize the fundamental ideas of cardiovascular medicine

The target of this specific overview is to offer you a operating realizing of the main ideas of cardiovascular body structure. Concise yet thorough, Cardiovascular Physiology makes a speciality of the proof you must get a superior mammoth photograph assessment of ways the cardiovascular approach operates below common and irregular occasions. there isn't any quicker or greater technique to learn the way the main rules of cardiovascular functionality observe to universal physiological and pathological demanding situations than this engagingly-written guide.

Features:

  • Clarifies the main points of physiologic mechanisms and their position in pathologic states
  • hyperlinks cardiovascular body structure to analysis and remedy
  • Summarizes key thoughts on the finish of every bankruptcy
  • Highlights must-know info with bankruptcy ambitions
  • Provides the appropriate quickly overview for the USMLE Step 1
  • Reinforces studying with examine questions on the finish of every bankruptcy
  • Keeps you modern at the most up-to-date study and advancements during this ever-changing field

The content material you must achieve an intensive figuring out of this crucial subject:
assessment of the Cardiovascular process, features of Cardiac Muscle Cells, the guts Pump, size of Cardiac functionality, Cardiac Abnormalities, The Peripheral Vascular process, Vascular regulate, valuable Venous strain: a trademark of Circulatory Hemodynamics, law of Arterial strain, Cardiovascular reaction to Physiological Stresses, Cardiovascular functionality in Pathological Situations.

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Extra info for Cardiovascular Physiology (Lange Physiology Series)

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Phosphorylation of titin modulates passive stiffness of cardiac muscle in a titin isoform-dependent manner. J Gen Physiol. 2005;125:257â 271. [PMID: 15738048] Gordon AM, Regnier M, Homsher E. " News Physiol Sci. 2000;16:49â 56. Hamilton SL, Serysheva I, Strasburg GM. Calmodulin and excitation-contraction coupling. News Physiol Sci. 2000;15:281â 284. [PMID: 11390927] Hiraoka M, Furukawa T. Functional modulation of cardiac ATP-sensitive K+ channels. News Physiol Sci. 1998;13:131â 137. [PMID: 11390776] Hume JR, Duan D, Collier ML, et al.

A muscle contr isotonically when lifting a fixed weight such as the 1-g load shown in Figure 2â 9. 5 g as indicated by the dashed line in the graph of Figure 2â 9. 5 g obviously canno generated while lifting a 1-g weight. When a muscle has contractile potential in excess of the tension it is actually developing, it shortens. Thus in an isotonic contraction, muscle length decreases at constant tension, as illustrated by horizontal arrow from point 1 to point 3 in Figure 2â 9. As the muscle shortens, however, its contractile potential inherently decreases, as indicated by the downward slope of the peak isometric tension curve in Figure 2â 9.

The ventricle has reached its minimum or end-systolic volume at the time of aortic valve closure. The amount of blood ejected from the ventricle during a single beat, the stroke volume, is equal to ventricular end-diastolic volume minus ventricular end-systolic volume. The aorta distends or balloons out during systole because more blood enters the aorta than leaves it. During diastole, the arterial pressure is maintained by the elastic recoil of walls of the aorta and other large arteries. Nonetheless, aortic pressure gradually falls during diastole as the aorta supplies blood to the systemic vascular beds.

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