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Neuro Lec 10-13

Total questions: 22

Worksheet time: 18mins

Name
Class
Date
1.

characteristics of the NMJ:

a)

small size

b)

accessible and relatively simple

c)

synaptic portions of 3 cells: MNs, muscle, Schwann

d)

high concentrations of things that are at low concentrations extrasynaptically

2.

NERVE action potential at the ____ ____ opens voltage-gated ____ ____

Ca2+ influx triggers ____ ____ ____ to presynaptic membrane and Ach ____

(a)  

3.

after Ach release, Ach diffuses across the ____ and binds to ____

____ moves in and ____ moves out

this causes postsynaptic membrane ____

(a)  

4.

after depol, if the ____ ____ voltage is reached, Na+ channels ____, and muscle AP ensues

(a)  

5.

which of the following is false

a)

presyn nerve terminal is filled with synaptic vesicles with ACh

b)

postsynaptic muscle membrane has a high degree of folding

c)

NMJ is covered by terminal Schwann cells

d)

NMJ does not cover terminal

6.

which are true

a)

postsynaptic depol > EPP

b)

EPP > AP threshold triggers opening of voltage-gated Na+ channels

c)

EPP - AP threshold = safety factor (ensures that EPP reliably activates myofibre)

d)

EPP depol myofibre > required for AP threshold

7.

ACh is ____ + ____, catalyzed by ____ (short form)

(a)  

8.

choline comes from extracellular fluid (transported by CHT1)

acetyl-CoA comes from mitochondria

a)

true

b)

false

9.

ACh is packed into ____ by VAChT

a)

secretory vesicles

b)

mitochondria

c)

synapses

d)

NMJs

10.

2-10% of ACh vesicles form the ____ ____ pool, which localize at ____ zones and are released upon arrival of ____ ____ and ____ influx

(a)  

11.

majority of ACh forms the ____ pool

vesicles recovered by ____ of presynaptic memb, and loaded locally with ____

____ busts ACh into choline and ____

(a)  

12.

what is the cytomatrix of the active zone

a)

AZ composed of dense collection of proteins

b)

proteins that tether synaptic vesicles to the presynap memb and mediate vesicular fusion

c)

large proteins at the NMJ AZs

d)

AZs loaded with NMJ synapses

13.

what is the SNARE complex?

a)

release of ACh mediated by vesicular membrane proteins and CAZ proteins

b)

synapsin shuttles ACh vesicles from reserve pool to AZs

c)

ACh vesicle docks at the AZ, undergoes nucleation & zippering

d)

Ca2+ causes fusion of vesicle and presynap memb, exocytosis

14.

positive signal: agrin is released from the ____ ____ and binds to the ____-____ complex

increases the level of ____ (NMJ protein)

(a)  

15.

positive signal: neuregulin is released from the ____ ____ and binds ____ receptors.

phosphorylation cascade that results in the phosphorylation of ____, which is a ____ ____

^ this binds to DNA elements in the _-___ to inc trans of NMJ proteins

(a)  

16.

positive signals supersede negative signals, resulting in high NMj (AChR)

a)

false

b)

true

17.

negative signal: initiated by ____ release, which triggers ____ influx, turning on the proteins that phosphorylate (inactivate) ____ protein

^that protein usually activates ____ transcription,

thfr less expression of NMJ genes

(a)  

18.

the DAPC is:

a)

a mechanical link b/w intraceullar cytoskeleton & extracellular matrix

b)

signal transduction system for cues from the external to reach the internal

c)

comprised of sarcoplasmic, transmemb, and extracellular proteins

d)

located all around the fibre

19.

UAPC vs DAPC

a)

Utrophin is not similar to dystrophin

b)

U is found more along the sarcolemma and D is found more around the NMJ

c)

U is at the crests of the junctional folds, D is at the troughs

d)

the complex itself (aside from U vs D) is identical

20.

testing techniques for dystrophin:

a)

muscle biopsies - plunge lidocaine needle into muscle and suction, take 2 150 mg samples, short recovery,

b)

IF tells us how much of something is expressed and where it is distributed

c)

results between Western blot and IF never conflict each other

d)

Western blot assess how much of something is expressed in the muscle

21.

muscles lacking dystrophin:

a)

have a lot of size variability

b)

go through successive rounds of degeneration/regeneration (almost no mature fibres)

c)

have peripheral nuclei

d)

have thick CT or adipose tissue in the muscle

22.

absence of dystrophin causes:

a)

reduction in the other members of the DAPC

b)

neuromuscular disorders, muscular dystrophies

c)

irregular muscle morphology

d)

musle fibres that are the same size