BMD221 Lecture 1: Electrical Properties of Cardiac Cells PDF

Summary

Lecture about the electrical properties of cardiac cells, giving the learning goals and including diagrams, and a quick review of neurons. Highlights the myogenic properties of the heart and explains how pacemaker cells work. The lecture also discusses funny channels, the role of G-proteins, and the conduction system of the heart. Discusses and visualises the mechanism of electrical conduction, and includes a summary of the key takeaways of the session.

Full Transcript

Electrical Properties of Cardiac Cells by Dr. Greg Szulgit learning goals: 1. Understand action potentials (APs) in general 2. Understand myogenic APs 3. Understand the conduction of waves of APs 4. Understand the contraction of cardiac muscle cells quick review of...

Electrical Properties of Cardiac Cells by Dr. Greg Szulgit learning goals: 1. Understand action potentials (APs) in general 2. Understand myogenic APs 3. Understand the conduction of waves of APs 4. Understand the contraction of cardiac muscle cells quick review of neurons As a student, your first exposure to action potentials (APs) was probably to those in the nervous system. learning goals: 1. Understand action potentials (APs) in general 2. Understand myogenic APs 3. Understand the conduction of waves of APs 4. Understand the contraction of cardiac muscle cells hearts are myogenic hearts can beat without neural stimulation https://www.youtube.com/watch?v=lmhBEeEMqYo another example (beware; lots of blood) https://www.youtube.com/watch?v=HYWmYJNg5Jw The pacemaker cells It starts with the sino- atrial node (SAN) The blue tissue exhibits spontaneous generation of APs How does this happen? Discuss this with your groups. AP in a pacemaker Here’s a hint. cell membrane potential (mV) time (ms) Describe this. “funny current” 1979 funny channels Funny funny channels channels and Note: There appear to T-Type be no ‘regular’ Na+ calcium channels in the channels are pacemaker cells in the voltage- apex of the SAN, so the gated, but sodium ion influx is they are also due to funny channels. opened by cAMP. When this happens, sodium and calcium ions enter cell. take home messages of previous slide: funny channels allow Na+ to enter and are only in pacemaker cells T-type calcium channels allow Ca2+ to enter transiently (quickly) and are only in pacemaker cells L-type calcium channels allow Ca2+ to enter long term and are in pacemaker cells and cardiomyocytes they are voltage-gated they are also activated by cAMP General point for biologists: Neurotransmitters and drugs often work indirectly through G- proteins 1994 Nobel prize in Physiology or Medicin There are many channels affected by G-proteins. AP in a pacemaker cell membrane potential (mV) time (ms) hearts are myogenic and here are isolated heart cells (cardiomyocytes) that have been growing and replicating in a pitri dish learning goals: 1. Understand action potentials (APs) in general 2. Understand myogenic APs 3. Understand the conduction of waves of APs 4. Understand the contraction of cardiac muscle cells conduction system special fibres The contractile that are made muscle tissue of muscle cells (the cells that wrapped in comprise this collagenous tissue are tissue* (these generally are generally referred to as referred to as cardiomyocytes) pacemaker. cells). cardiac skeleton (aka skeleton of the heart) the conduction system is also surrounded by fibrous (collagenous)*The tissue evidence for connective tissue around the pacemaker bundles is difficult and contentious. what does the cardiac skeleton do? 1. structural 2. guides and insulates electrical conduction down the specialised muscle cells within 3. causes electrical waves passing through heart muscle to pause between atria and ventricles T-tubules (an extension of the membrane sarcolemma) (sarcolemma) myofibril mitochondria to sarcoplasmic sarcomere supply lots of reticulum (holds (banded by z-disks) energy lots of Ca++) cardiac muscle cells (cardiomyocytes) are conductive fluorescent labeling for connexin (the protein that makes gap junctions) Gap junctions are important to keep the APs flowing to neighboring cells. Here’s what it looks like all together (from a gif on Wikipedia). With waves, timing is everything! learning goals: 1. Understand action potentials (APs) in general 2. Understand myogenic APs 3. Understand the conduction of waves of APs 4. Understand the contraction of cardiac muscle cells T-tubules (an extension of the membrane sarcolemma) (sarcolemma) myofibril sarcomere mitochondria to sarcoplasmic (banded by z-disks) supply lots of reticulum (holds energy lots of Ca++) in skeletal muscle in cardiac muscle Not only is Ca2+ shuttled across the membrane of the sarcoplasmic reticulum, it is also allowed to flow in from the T-tubules across the cell membrane via L- type channels. in cardiac muscle The incoming Ca2+ will activate ryanodine receptors. These are Ca2+ channels that are activated by Ca2+ (so, even more Ca2+ comes out). cardiomyocyte AP Effective Refractory Period. Note that cardiomyocy tes cannot be re- stimulated for a long time compared with skeletal muscle. in cardiac muscle The reason that the potassium permeability looks so complicated is that there are at least different K+ currents. Question: why are the rising slopes different? (f) = “funny” NOT “fast” learning goals: 1. Understand action potentials (APs) in general 2. Understand myogenic APs 3. Understand the conduction of waves of APs 4. Understand the contraction of cardiac muscle cells Coda: Let me show you a magic trick. Don’t take things for granted as blasé just because we are used to them. Consciousness is the holy grail of biology. Stay curious!

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