Cardiovascular- Physiology Flashcards
Do Purkinje fibers and the Bundle of His undergo action potentials that resemble ventricular muscle tissue or pacemaker cells?
Ventricular Muscle Tissue
What occurs during phase 0 of ventricular action potential?`
Fast acting sodium channels open and sodium floods into the cell
What occurs during phase 1 of ventricular action potential?
Voltage-gated potassium channels open and potassium goes down its concentration gradient and leaves the cell.
What occurs during phase 2 of ventricular action potential?
Voltage-gated calcium channels open and calcium enters the cell directly balancing potassium current.
What occurs during phase 3 of ventricular action potential?
Calcium channels close and potassium continues to flow out of the cell.
What occurs during phase 4 of ventricular action potential?
Voltage-gated potassium channels are closed but high potassium permeability. So potassium is leaking into the cell and sodium and calcium are exiting
What occurs during phase 0 of pacemaker action potential?
L-type calcium channels open and calcium enters the cell
What occurs during phase 3 of pacemaker action potential?
L-type calcium channels close and potassium channels open allowing for the exit of positively charged potassium
What occurs during phase 4 of pacemaker action potentials?
Early in phase 4- low potassium current and funny current occurs allowing sodium to enter the cell.
Late in phase 4- T-type calcium channels open allowing calcium to enter cell.
What two tissues make up pacemaker action potentials?
SA and AV node
What seven drugs can cause a severe decreased in potassium which can lead to prolonged QT?
Some Risky Meds Can Prolong QT: Sotalol Risperidone Macrolides Chloroquines Protease Inhibitors (-navir) Quinidine Thiazides
What is torsades de pointes likely to progress to?
Ventricular fibrillation
How do you treat torsades de pointes?
Magnesium sulfate
What causes congenial long QT?
It is an inherited disorder of myocardial repolarization, typically due to ion channel defects; this leads to increased risk of sudden cardiac death due to torsades de pointes
What is Romano-Ward Syndrome?
A congenital long QT syndrome. It is autosomal dominant and produces a pure cardiac phenotype (no deafness)