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SMOOTH MUSCLE SMOOTH MUSCLE

SMOOTH MUSCLE - PowerPoint Presentation

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Uploaded On 2016-07-15

SMOOTH MUSCLE - PPT Presentation

Dr Ayisha Qureshi MBBS MPhil Assistant Professor CLASSIFICATION OF SMOOTH MUSCLES UNITARY SINGLE UNITSYNCYTIALVISCERAL Muscles of visceral organs eg GIT uterus ureters amp some of the smaller blood vessels ID: 405459

amp muscle myosin smooth muscle amp smooth myosin contraction actin skeletal presence mechanism control cells overlap cell filaments troponin

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Slide1

SMOOTH MUSCLE

Dr.

Ayisha

Qureshi

MBBS, MPhil

Assistant ProfessorSlide2

CLASSIFICATION OF SMOOTH MUSCLES

UNITARY/ SINGLE UNIT/SYNCYTIAL/VISCERAL

Muscles of visceral organs .e.g. GIT, uterus, ureters & some of the smaller blood vessels.

Form a sheet or bundles of tissue.Cell membranes show gap junctions that allows AP to pass rapidly from cell to cell.AP spreads rapidly throughout the sheet of cells – cells contract as a single unit.

MULTI-UNIT

Iris &

Ciliary

body of the eye, large arteries,

Piloerector

muscles

Showing discrete, individual smooth muscle fibers.

Smooth muscle cells not electrically linked. Each muscle fiber innervated by a single nerve ending. NT itself can spread and lead to an AP.

Selective activation of each muscle fiber that can then contract independently of each other.Slide3
Slide4

Latch mechanism

It is a state in which the dephosphrylated myosin remains attached to actin for prolonged period of time. This produces sustained contraction without consuming ATP & thus enables the smooth muscle to sustain long-term maintenance of tone without fatigue. E.g. urinary bladder full of urine.Slide5

COMPARISON OF SKELETAL & SMOOTH MUSCLE CONTRACTION:Slide6

COMPARISON OF SKELETAL & SMOOTH MUSCLE CONTRACTION:

S.NO

CHARACTERISTICS

SKELETAL

MUSCLE

SMOOTH MUSCLE

1.

Location

Attached to the skeleton

Blood vessels, hollow organs, eye

2.

Mechanism

of contraction

Sliding filament

Sliding

filament

3.

Nerve supply

Motor neurons

Autonomic nervous system

4.

Level of control

Under

Voluntary control

Under Involuntary control

5.

Presence

of Thick & Thin filaments

Yes

Yes

6.

Presence

of

Tropomyosin

Yes

Yes

7.

Presence of Troponin

Yes

No

8.

Presence of T-tubules

Yes

No

9.

Level of development

of Sarcoplasmic Reticulum

Well Developed

Poorly

DevelopedSlide7

S.no

CHARACTERISTICS

SKELETAL

MUSCLE

SMOOTH MUSCLE

10.

Source of Calcium

Sarcoplasmic

Reticulum (SR)

ECF

& SR

11.

Overlap of Actin & Myosin

Overlap

of actin & myosin seen only in part of the A-band

Continuous overlap

of actin & myosin, b/c of side-polar cross bridges

12.

ATP used directly

by contractile apparatus

Yes

Yes

13.

Myosin ATPase activity;

speed of contraction

Fast or slow depending on type of fiber

Very slow

14.

Site of

Calcium regulation

Troponin in thin filaments

Myosin in thick filaments

15.

Mechanism of Calcium action

Physically repositions troponin-

tropomyosin

complex to uncover actin cross-bridge binding site

Chemically brings

about phosphorylation

of myosin cross

bridges so they can bind with actin Slide8

S.no

CHARACTERISTICS

SKELETAL

MUSCLE

SMOOTH MSUCLE

16.

Duration of contraction

100- 200

msec

Upto

5 sec

17.

Presence of Gap junctions

No

Yes

18.

Latch mechanism

No

Yes

19.

NMJ

Yes

No

20.

Neurotransmitter

Ach

only

Ach & Norepinephrine