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Phase Y Resting
↑
Phase :
:
.
Phase 2 mesing i am intaine
a
Plateau
:
van Repolarization
Ecax due to channel inactivation
Phase 3 :
:
Back to Phase 4
4
80
->
UK = -
50
at
IkI +
50
-......
↑gl
↑:
+20
-
0
-
.... -
At
Gia p
. .
-------------
mV
-
-
- - -
.....
At 0
Gea
-
50
-
↑
- - - -
-
. . . . -
0
gla
Y 4
-
90
I
R
M
systolic wave
P T Diastole P
wave
z M z
W
and
isoelectic
line
as
repolarization
as
C9 3)
"
During &RS Complex Repolarization ,
causes relevation
of heart (T-waves
↑
08
Time
(sec)
: see diagam
above
(Yaxis]
SA mode
His
AU mode ,
bundle
of
ventricles
⑧
⑧
⑰
e
⑱
and
signals can be sent
faster This can lead to shorter PR intervals , narrower GRS complex and altered
.
T-wave
(shape/amplitude) .
Electrical Depolarization occurs in the direction
of
lead
+ve
generating ve
deflection
.
+
:
in most
GRS complex Venticular depolarization from bundle of His & Packinge fibers usually (+ve) deflection
:
:
ventricular to
T-wave
repolarization from epicardium endocardium usually (tvel deflection
:
:
blue black
,
50
7 ⑦. .π@
⑦
⑲ ..
↑gl
membrane ......
"T-
----- -
20
+
potential
l
-
+40
---- - - --
.... - -
50
-
(mv)
Y 4
o 90
-
phase Time
( ms]
Fors involved
:
Nas it, c
Threshold
-
53
failed initiations
-
TO -
-
-
Resting potential
undershoot
⑧ I 2 3 U 5
Time (seconds)
motor action
nemon
potentials
Candionyoctes are basic units
of contraction in heart -
by laye gap junctions to serve as low resistance electrical pathways to allow safe conduction
ICDs maintain structural issue
integrity &
syctonized contraction
of cardiac
vascular smooth Cardiac Muscle Cells
Muscle Cells in them prevents
Presence
of desmosomes
stretch cannot cause contraction cells from pulling apart during stress of
generally usually
, under control
of
ANS individual
fibels contracting .
Macula adherens
cells
(hyperplasia)
* Do not contain * Contain Sarcolemma
sanolleme ↓
* Contain invaginations called
tansports substrates & out
of cell
&
in
I
calveolae attach
to increase location for intreat extracellular proteins
to .
·
enables
clustering of specific
groups of io channels &
receptors important in
cellular
signal transduction
multi-unit SMCs
single-unit SMCs
>
interconnected by gap junctions -> not as
strongly interconnected
lead
synchronized allows more
->
of contraction
to contractions -
control
precise
In blood vessels ,
multi-unit like VSMCs couple to form independently functioning units
that act as individual units (without syncytium) .
.
:
↳ ins
J
I membrane /and
physically move ergo conformat and changes
also lead
depolarization to channel activation
may
↳ and membrane
selective
hyperpolarization
for specific ious
leads to return to rest state .
ligand binds to
receptors on ion channel inducing
,
conformational change in channel protein
-can be due to direct interaction with
ligandl / through intracellular
signaling pathways
.
V =
Difference potential
in
energy allows movement against any other forces .
It stores energy More
capacitance charge stored for voltage
be
meas more cn
given
.
Nat, K etc
B Yes
key stone voltage in terms ions
of
.
. .
C Capacitance is measure
of apacitor's ability to
·
1 - chaye stored on
capacitor in coulombs
↓
V volts
capacitors
voltage
across in
Capacitance
in farads
D
Especific - I x = 12x109F(a
are ,
is
state of Diffusion constant
Steady means Rate remains over time
.
-
perfick's Law
in
=
-
as
Raffian coefficient
0
concentration caresmicPet
hae