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PHYSIOLOGY 1 LECTURE 25 CARDIAC MUSCLE EXCIT. - CONT. - COUPL. ACTION POTENTIALS.

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Presentation on theme: "PHYSIOLOGY 1 LECTURE 25 CARDIAC MUSCLE EXCIT. - CONT. - COUPL. ACTION POTENTIALS."— Presentation transcript:

1 PHYSIOLOGY 1 LECTURE 25 CARDIAC MUSCLE EXCIT. - CONT. - COUPL. ACTION POTENTIALS

2 Cardiac Muscle n Cardiac muscle differs from both smooth muscle and skeletal muscle, being somewhere in between the two. Therefore, cardiac muscle is considered an intermediate form between the more primitive smooth muscle and advanced skeletal muscle. Thus, it has properties of both smooth and skeletal muscle as well as it’s own unique properties.

3 Cardiac Muscle Structure n SIZE - Cardiac muscle tends to be smaller than skeletal muscle but larger than smooth muscle. About 10 to 15  m in diameter and around 50  m in length. Cardiac muscle tends to be smaller than skeletal muscle but larger than smooth muscle. About 10 to 15  m in diameter and around 50  m in length.

4 Cardiac Muscle Structure n Contractile Proteins- n In cardiac muscle the contractile proteins are isomers of the skeletal muscle sarcomeres and operate in a similar manner.

5 Cardiac Muscle Structure n T- Tubules - n In cardiac muscle only one T -tubule occurs per sarcomere and Triad formation is somewhat more rudimentary due to the small size of the sarcoplasmic reticulium.

6 Cardiac Muscle Structure n Organelles - n Cardiac muscle is normally mononucleated but a few may be multinucleated. Otherwise organelles are similar to most other cells with the exception of the SR

7 Cardiac Muscle Structure n The SR in cardiac muscle cells is similar to smooth muscle and takes up less than 5% of cellular volume. Therefore, it lacks space for large amounts of Ca++ and the cell is dependent on external Ca++ for contraction.

8 Cardiac Muscle Structure n Intercellular Connections - n Cardiac muscle cells are connected by a intercalated disk. In reality these are interdigitated bundles of tightly bound collagen and elastin fibers containing many gap junctions (An electrical syncytium)

9 Cardiac Muscle Structure n Sarcomere Size - Due to the very heavy quantity of connective tissue surrounding cardiac myocytes the resting sarcomere length is somewhat compressed at 1.6  M. Due to the very heavy quantity of connective tissue surrounding cardiac myocytes the resting sarcomere length is somewhat compressed at 1.6  M.

10 Cardiac Muscle Structure n There are four types of cardiac muscle histologically “P” cells or pacemaker cells, transition cells, Purkinje cells, and normal cardiomyocytes. All of these are classified as cardiac muscle cells. However the “P”, transition, and Purkinje cells are all part of what is known as the cardiac conduction system and do not participate in muscle contraction but generate and transmit the cardiac action potential.

11 Cardiac Muscle Structure

12 Cardiac Muscle Excitation - Contraction - Coupling n In cardiac muscle external Ca ++ is once again required due to the small volume of the SR. n 1. Calcium induced calcium release n 2. Mechanism of calcium influx n 3. Role of calcium in tension development n 4. Relaxation and calcium efflux

13 Cardiac Muscle Excitation - Contraction - Coupling n Calcium Induced Calcium Release - n Passage of the cardiac action potential opens the slow calcium/sodium voltage gated channels. Ca ++ influx opens Ca ++ sensitive calcium channels in the SR.

14 Cardiac Muscle Excitation - Contraction - Coupling n Mechanism of Calcium Influx - n Calcium will influx through the slow voltage gated channels. But catacholamines also activate cAMP which in turn activates a cAMP dependent Protein Kinase which phosphoralates Ca ++ channels causing them to open increasing [Ca ++].

15 Cardiac Muscle Excitation - Contraction - Coupling n Role of Ca++ in Tension development - n Increased cytosolic Ca ++ concentrations increase crossbridge cycling rates thereby, increasing both the force and speed of myocyte contraction.

16 Cardiac Muscle Excitation - Contraction - Coupling n Calcium release from the SR and extracellular Ca++ bind to Troponin C and excitation contraction coupling proceeds as in skeletal muscle.

17 Cardiac Muscle Excitation - Contraction - Coupling n Relaxation and Calcium efflux - n Calcium is removed from the cardiac muscle cytosol by our standard Ca ++ ATPase into the SR and into the interstitial space, but it is joined by a Na + Ca ++ exchanger 1 Ca ++ out for 3 Na + in.

18 Cardiac Muscle Fast Cardiac Action Potential n There are two cardiac action potentials produced by coronary myocytes, the fast AP and the slow AP. The fast cardiac action potential is characterized by containing a plateau phase. We will take up the slow cardiac AP when we discuss the conduction system of the heart.

19 Cardiac Muscle Fast Cardiac Action Potential n The Fast Cardiac Action Potential - n Four phases n Phase 4 or resting phase (Not really a steady resting phase but rises slightly toward threshold) n Inwardly rectifying potassium current.

20 Cardiac Muscle Fast Cardiac Action Potential n Phase 0 - n Phase 0 of the fast cardiac action potential is due to the opening of the fast Na+ voltage gated channel similar to the ones encountered in nerve and skeletal muscle action potentials.

21 Cardiac Muscle Fast Cardiac Action Potential n Phase 1 - n Phase 1 of the fast cardiac action potential is due to a transient outward potassium current.

22 Cardiac Muscle Fast Cardiac Action Potential n Phase 2 - Plateau n Phase 2 of the fast cardiac action potential is due to a slow inward calcium, sodium channel balanced by three separate outward potassium currents.

23 Cardiac Muscle Fast Cardiac Action Potential n Phase 3 - Repolarization n Phase 3 of the fast cardiac action potential is due to the action of the voltage gated potassium channels and a decline in calcium/sodium conductance.

24 Cardiac Muscle Fast Cardiac Action Potential n Refractoriness - n Due to the long plateau phase ( phase 2) of the fast cardiac action potential the cardiac cells have time to contract before the action potential is finished. Can not generate tetany.


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