Electrical Synapse - McCool - Exam 1 Flashcards
•The resting membrane potential (Vm) of the cell is equal to the summed contribution by individual permeant __ ___.
•The resting membrane potential (Vm) of the cell is equal to the summed contribution by individual permeant ion potentials
- The equilibrium potential of ___ ___ determine the membrane potential
- Ionic permeability depends on: ____, “____” or leak
There are also active transport mechanisms
•__ ___ (charge distribution)
- The equilibrium potential of individual ions determine the membrane potential
- Ionic permeability depends on: Diffusion, “Channels” or leak
There are also active transport mechanisms
•Electrical potential (charge distribution)
What are the four characteristics of an AP?
- Threshold
•A critical level of depolarization is required to generate an AP.
- All or None
•Once initiated, it will run its course regardless of the stimulus.
An inherent property of the membrane.
- Five Phases – constant
•Depolarization (1), overshoot (Vm>0mV) (2), repolarization (3), after-hyperpolarization(4), recovery (5)
- Refactory Period
Refractory Periods:
- __ ___ period – impossible to initiate another AP
- __ __ period – possible to initiate, but has higher threshold and smaller amplitude
•Absolute refactory period – impossible to initiate another AP
•Relative refactory period – possible to initiate, but has higher threshold and smaller amplitude
What mechanisms control the characteristics of the Action Potential?
- Sodium-dependence of the overshoot (not repolarization or after-hyperpolariztion)
- Ion-selective “channels” control the action potential
Voltage-gated K+ channels
- Selective for K+
- 10,000X more effective than ___+
- Na+ – 0.95Å; K+ – 1.33Å
•Pharmacology
•____ (bee venom)
•Subunit structure
____ subunits
- MANY ____
- Distinct from ‘____’ K channels and ____-activated K channels
Voltage-gated K+ channels:
- Selective for K+
- 10,000X more effective than Na+
- Na+ – 0.95Å; K+ – 1.33Å
•Pharmacology
•Apamin (bee venom)
- Subunit structure
- Four subunits
- MANY isoforms
- Distinct from ‘leak’ K channels and hyperpolarization-activated K channels
Voltage-Gated Sodium Channels
- Subunit structure (K-channel X 4)
- Nine distinct genes
- NaV 1.1-1.9
- Highly similar
- Tissue distribution
- Pharmacology
- Local anesthetics
- Novacaine, Lidocaine
- Anti-epileptics
- Anti-arrhythmics (lidocaine)
Many naturally occuring toxins (tetrodotoxin, saxitoxin, scorpion toxins
Voltage-Gated Sodium Channels
- Subunit structure (K-channel X 4)
- Nine distinct genes
- NaV 1.1-1.9
- Highly similar
- Tissue distribution
- Pharmacology
- Local anesthetics
- Novacaine, Lidocaine
- Anti-epileptics
- Anti-arrhythmics (lidocaine)
Many naturally occuring toxins (tetrodotoxin, saxitoxin, scorpion toxins
Voltage gated Ca++ channels:
- Subunit structure – similar to sodium channels
- Accessory subunits
- a2/d, b, g – expression/function
- Pharmacology
- La3+, Co2+, Cd2+
- Conotoxins, agatoxins
- Natural toxins/paralytics
•Antihypertensives
- Dihyropyridines (nitrendipine, nifedipine)
- Diltiazem, Verapamil
•Anti-arrhythmics
•Verapamil
•Positive Modulators
•Beta adrenergic receptors
Voltage gated Ca++ channels:
- Subunit structure – similar to sodium channels
- Accessory subunits
- a2/d, b, g – expression/function
- Pharmacology
- La3+, Co2+, Cd2+
- Conotoxins, agatoxins
- Natural toxins/paralytics
•Antihypertensives
- Dihyropyridines (nitrendipine, nifedipine)
- Diltiazem, Verapamil
•Anti-arrhythmics
•Verapamil
•Positive Modulators
•Beta adrenergic receptors