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BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

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Page 1: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

BIOELECTRICITY AND EXCITABLE TISSUE

THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK

D. C. Mikulecky Department of Physiology andFaculty Mentoring Program

Page 2: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE RESTING CELL

HIGH POTASSIUMLOW SODIUMNA/K ATPASE PUMP RESTING POTENTIAL ABOUT 90

- 120 MVOSMOTICALLY BALANCED

(CONSTANT VOLUME)

Page 3: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program
Page 4: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

BIOELECTRICITY

THE ORIGIN OF THE MEMBRANE POTENTIAL

Page 5: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

MOBILITY OF IONS DEPENDS ON HYDRATED SIZE

IONS WITH SMALLER CRYSTAL RADIUS HAVE A HIGHER CHARGE DENSITY

THE HIGHER CHARGE DENSITY ATTRACTS MORE WATER OF HYDRATION

THUS THE SMALLER THE CRYSTAL RADIUS, THE LOWER THE MOBILITY IN WATER

Page 6: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

IONS MOVE WITH THEIR HYDRATION SHELLS

- +- +- +

- +

Hydration Shells

- +

- +

-

+

- +

- +- +

-

+

-

+

- +

- +-

+

-

+

- +

- +

- +

- +

- +

- +

- + -

+

- +

- +

Page 7: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

ELECTRONEUTRAL DIFFUSSION

HIGH SALT CONCEMTRATION

LOW SALT CONCEMTRATION

+

-

BARRIER SEPARATES THE TWO SOLUTIONS

+

-+

-

+

-+

-+

-

+

-

+

-

Page 8: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

ELECTRONEUTRAL DIFFUSSION

HIGH SALT CONCEMTRATION

LOW SALT CONCEMTRATION

+

-

BARRIER REMOVED

+

-

+

-

+

-+

-+

-+

-

+-

+ -

CHARGE SEPARATION = ELECTRICAL POTENTIAL

Page 9: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

ELECTRICAL POTENTIAL=CHARGE SEPARATION

In water, without a membrane hydrated Chloride is smaller than hydrated Sodium, therefore faster:

Cl-

Na+

The resulting separation of charge is called an ELECTRICAL POTENTIAL

+ -

Page 10: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE MEMBRANE POTENTIAL

MEMBRANE

ExtracellularFluid

IntracellularFluid

Na+

K+

Sodium channel is less open causing sodium to be slower

Potassium channel is more open causing potassium to be faster + - MEMRANE POTENTIAL

(ABOUT 90 -120 mv)

Page 11: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE ORIGIN OF BIOELECTRICITY

POTASSIUM CHANNELS ALLOW HIGH MOBILITY

SODIUM CHANNELS LESS OPENCHARGE SEPARATION OCCURS

UNTIL BOTH MOVE AT SAME SPEED STEADY STEADY IS ACHIEVED

WITH A CONSTANT MEMBRANE POTENTIAL

Page 12: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE RESTING CELL

HIGH POTASSIUMLOW SODIUMNA/K ATPASE PUMP RESTING POTENTIAL ABOUT 90

- 120 MVOSMOTICALLY BALANCED

(CONSTANT VOLUME)

Page 13: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program
Page 14: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

ACTIVE TRANSPORT

ADP

ATP

Page 15: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

ACTIVE TRANSPORT REQUIRES AN INPUT OF ENERGY

USUALLY IN THE FORM OF ATPATPase IS INVOLVEDSOME ASYMMETRY IS

NECESSARYCAN PUMP UPHILL

Page 16: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

EXCITABLE TISSUES

NERVE AND MUSCLEVOLTAGE GATED CHANNELSDEPOLARIZATION LESS THAN

THRESHOLD IS GRADEDDEPOLARIZATION BEYOND

THRESHOLD LEADS TO ACTION POTENTIAL

ACTION POTENTIAL IS ALL OR NONE

Page 17: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE NERVE CELL

CELLBODY

DENDRITES

AXON

AXONHILLOCK

AXONTERMINALS

Page 18: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

EXCITABLE TISSUES:THE ACTION POTENTIAL

THE MEMBRANE USES VOLTAGE GATED CHANNELS TO SWITCH FROM A POTASSIUM DOMINATED TO A SODIUM DOMINATED POTENTIAL

IT THEN INACTIVATES AND RETURNS TO THE RESTING STATE

THE RESPONSE IS “ALL OR NONE”

Page 19: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

FOR EACH CONCENTRATION DIFFERENCE ACROSS THE MEMBRANE THERE IS AN ELECTRIC POTENTIAL DIFFERENCE WHICH WILL PRODUCE EQUILIBRIUM.

AT EQUILIBRIUM NO NET ION FLOW OCCURS

EQUILIBRIUM POTENTIALS FOR IONS

Page 20: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE EQUILIBRIUM MEMBRANE POTENTIAL FOR POTASSIUM IS -90 mV

+ -CONCENTRATION

POTENTIALK+ K+

IN

Page 21: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE EQUILIBRIUM MEMBRANE POTENTIAL FOR SODIUM IS + 60 mV

Na+Na+

+-CONCENTRATION

POTENTIAL

INOUT

Page 22: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE RESTING POTENTIAL IS NEAR THE POTASSIUM EQUILIBRIUM POTENTIAL

AT REST THE POTASSIUM CHANNELS ARE MORE OPEN AND THE POTASSIUM IONS MAKE THE INSIDE OF THE CELL NEGATIVE

THE SODIUM CHANNELS ARE MORE CLOSED AND THE SODIUM MOVES SLOWER

Page 23: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

EVENTS DURING EXCITATION

DEPOLARIZATION EXCEEDS THRESHOLDSODIUM CHANNELS OPENMEMBRANE POTENTIAL SHIFTS FROM

POTASSIUM CONTROLLED (-90 MV) TO SODIUM CONTROLLED (+60 MV)

AS MEMBRANE POTENTIAL REACHES THE SODIUM POTENTIAL, THE SODIUM CHANNELS CLOSE AND ARE INACTIVATED

POTASSIUM CHANNELS OPEN TO

REPOLARIZE THE MEMBRANE

Page 24: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

OPENING THE SODIUM CHANNELS ALLOWS SODIUM TO RUSH IN

THE MEMBRANE DEPOLARIZES AND THEN THE MEMBRANE POTENTIAL APPROACHES THE SODIUM EQUILIBRIUM POTENTIAL

THIS RADICAL CHANGE IN MEMBRANE POTENTIAL CAUSES THE SODIUM CHANNELS TO CLOSE (INACTIVATION) AND THE POTASSIUM CHANNELS TO OPEN REPOLARIZING THE MEMBRANE

THERE IS A SLIGHT OVERSHOOT (HYPERPOLARIZATION) DUE TO THE POTASSIUM CHANNELS BEING MORE OPEN

Page 25: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

GRADED VS ALL OR NONE

A RECEPTOR’S RESPONSE TO A STIMULUS IS GRADED

IF THRESHOLD IS EXCEEDED, THE ACTION POTENTIAL RESULTING IS ALL OR NONE

Page 26: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program
Page 27: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program
Page 28: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

PROPAGATION OF THE ACTION POTENTIAL

+++++

--------

---------------------

+++++++++++++AXON MEMBRANE

INSIDE

OUTSIDEACTION POTENTIAL

DEPOLARIZINGCURRENT

Page 29: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

PROPAGATION OF THE ACTION POTENTIAL

+++++

--------

---------------------

+++++++++++++AXON MEMBRANE

INSIDE

OUTSIDEACTION POTENTIAL

DEPOLARIZINGCURRENT

Page 30: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

PROPAGATION OF THE ACTION POTENTIAL

--+++

++------

+++------------------

---++++++++++AXON MEMBRANE

INSIDE

OUTSIDEACTION POTENTIAL

DEPOLARIZINGCURRENT

Page 31: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

PROPAGATION OF THE ACTION POTENTIAL

--------

+++++

++++++-------

-----------++++AXON MEMBRANE

INSIDE

OUTSIDEACTION POTENTIAL

DEPOLARIZINGCURRENT

Page 32: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

SALTATORY CONDUCTION

+++++

--------

--------

+++++AXON MEMBRANE

INSIDE

OUTSIDEACTION POTENTIAL

DEPOLARIZINGCURRENT

MYELINNODE OFRANVIER

NODE OFRANVIER

Page 33: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

NORMALLY A NERVE IS EXCITED BY A SYNAPSE OR BY A RECEPTOR

MANY NERVES SYNAPSE ON ANY GIVEN NERVE

RECEPTORS HAVE GENERATOR POTENTIALS WHICH ARE GRADED

IN EITHER CASE WHEN THE NERVE IS DEPOLARIZED BEYOND THRESHOLD IT FIRE AN ALL-OR-NONE ACTION POTENTIAL AT THE FIRST NODE OF RANVIER

Page 34: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program
Page 35: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

JUNCTION BETWEEN TWO NEURONSCHEMICAL TRANSMITTERMAY BE 100,000 ON A SINGLE CNS

NEURONSPATIAL AND TEMPORAL

SUMMATIONCAN BE EXCITATORY OR INHIBITORY

Page 36: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

SYNAPTICVESSICLES

•••

•••

••• •••

•••

•••

•••

•••

•••

INCOMINGACTION POTENTIAL

CALCIUM CHANNEL

IONCHANNEL

RECEPTOR

ENZYME

Page 37: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

SYNAPTICVESSICLES

•••

•••

••• •••

•••

•••

•••

•••

•••

INCOMINGACTION POTENTIAL

CALCIUM CHANNEL

IONCHANNEL

RECEPTOR

ENZYME

Page 38: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

SYNAPTICVESSICLES

•••

•••

••• •••

•••

•••

•••

•••

•••

INCOMINGACTION POTENTIAL

CALCIUM CHANNEL

IONCHANNEL

RECEPTOR

ENZYME

Page 39: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

SYNAPTICVESSICLES

•••

•••

•••

•••

•••

•••

•••

•••

•••

CALCIUM CHANNEL

IONCHANNEL

RECEPTOR

ENZYME

Page 40: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

SYNAPTICVESSICLES

•••

••• •••

•••

•••

•••

•••

•••

•••

CALCIUM CHANNEL

IONCHANNEL

RECEPTOR

ENZYME

•••

Page 41: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

SYNAPTICVESSICLES

•••

•••

••• •••

•••

•••

•••

•••

•••

CALCIUM CHANNEL

IONCHANNEL

RECEPTOR

ENZYME

Page 42: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

THE SYNAPSE

SYNAPTICVESSICLES

•••

••• ••• •••

•••

•••

•••

•••

•••

CALCIUM CHANNEL

IONCHANNEL

RECEPTOR

ENZYME

Page 43: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

POSTSYNAPTIC POTENTIALS

RESTINGPOTENTIAL

IPSP EPSP

TIME

Page 44: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

TEMPORAL SUMMATION

TIME

TOO FAR APART IN TIME:NO SUMMATION

Page 45: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

TEMPORAL SUMMATION

TIME

CLOSER IN TIME: SUMMATION BUT BELOW THRESHOLD

THRESHOLD

Page 46: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

TEMPORAL SUMMATION

TIME

STILL CLOSER IN TIME: ABOVETHRESHOLD

THRESHOLD

Page 47: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

SPATIAL SUMMATION

TIME

SIMULTANEOUSINPUT FROM TWOSYNAPSES: ABOVETHRESHOLD

THRESHOLD

Page 48: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

EPSP-IPSP CANCELLATION

Page 49: BIOELECTRICITY AND EXCITABLE TISSUE THE ORIGIN OF BIOELECTRICITY AND HOW NERVES WORK D. C. Mikulecky Department of Physiology and Faculty Mentoring Program

NEURO TRANSMITTERS

ACETYL CHOLINEDOPAMINENOREPINEPHRIN

EEPINEPHRINESEROTONIN

HISTAMINEGLYCINEGLUTAMINEGAMMA-

AMINOBUTYRIC ACID (GABA)