Nerves and Muscle Flashcards

1
Q

Identify the key features and cells in the histological section of the three muscle types.

A

skeletal - peripheral and multinucleated, striated, t-tublules present, no cell to cell junctions

smooth - spindle shaped, no striations, single nucleus, calcium for contraction, gap junctions

cardiac - gap junctions and intercalated disks, cross striations, branched

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2
Q

Measure conduction velocity in human motor neurones.

A

The nerve conduction velocity (speed) is then calculated by measuring the distance between electrodes and the time it takes for electrical impulses to travel between electrodes. A related procedure that may be performed is electromyography (EMG).

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3
Q

Describe the design, strengths and limitations of case-control studies

A

compares people with and without disease, no follow up, efficient for rare diseases, multiple exposures can be studied, prone to bias, needs precise case definition

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4
Q

Describe how to select case and control groups

A

case - need to decide whether to use incident or prevalent cases, source and eligibility criteria needs to be considered

control - best controls are from the same pool as cases, more controls increase precision of odds ratio

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5
Q

Describe types of bias which may affect epidemiological studies, including selection bias, recall bias, response bias and interview bias

A

selection bias - proper randomization is achieved

recall bias - participants may recall their exposures differently based on if they’re a case or control.

response bias - participants respond to questions about their exposure in the way they think is expected.

interviewer bias - person collecting exposure data introduces their own bias.

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6
Q

Recognise the basic ways in which muscle proteins are degraded and their involvement in cachexia.

A

muscle proteins can be degraded by the ubiquitin proteasome degradation system, by autophagy via the lysosome, or by calcium activated proteases.

cachexia - muscle breakdown exceeds synthesis, muscle atrophy occurs

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7
Q

Explain the concept of nitrogen balance.

A

when in balance, nitrogen intake is equal to output. it can be positive in growing children and pregnant women, and negative during starvation or illness.

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8
Q

Recognise the requirement for essential amino acids.

A

essential amino acids must come from our diet as they cannot be synthesised.

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9
Q

Explain the processes of transamination (requiring pyridoxal phosphate as a cofactor) and oxidative deamination, in order to produce ammonium ions.

A

transamination - alpha amino acid + alpha ketoglutarate >< alpha keto-acid + glutamate

oxidative deamination - forms ammonium ion from glutamate

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10
Q

Describe how urea is synthesised.

A

through the urea cycle (google)

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11
Q

Explain the concept of glucogenic and ketogenic amino acids.

A

glucogenic - carbon skeletons increase the concentration of glucose

ketogenic - carbon skeletons increase the concentration of ketone bodies

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12
Q

Explain the relevance of the genetic code.

A

Genetic code is the amino acid basis for all organisms

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13
Q

Explain why the genetic code must be at least three bases per codon.

A

A doublet code of 2 bases per codon would be insufficient as this would lead to 16 doublets when 20 amino acids are needed. A triplet code is sufficient, which gives 64 different triplets of bases. A triplet code allows amino acids to be specified by more than one codon - it is degenerate.

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14
Q

Explain why the genetic code is degenerate but not ambiguous.

A

specific amino acids code for specific proteins.

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15
Q

Explain the relevance of nonsense codons.

A

Stop codons are also called nonsense codons because they do not code for an amino acid and instead signal the end of protein synthesis.

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16
Q

Describe in detail the chemical mechanisms involved in tRNA charging.

A

Before an amino acid can be incorporated into a growing polypeptide, it must first be attached to a molecule called transfer RNA, or tRNA, in a process known as tRNA charging. The charged tRNA will then carry the activated amino acid to the ribosome.

17
Q

Describe the process of Classical Conditioning.

A

using an unconditioned stimulus and a conditioned stimulus to produce an unconditioned response. the conditioned stimulus is then used to produce a conditioned response.

18
Q

Describe the process of Operant Conditioning.

A

there is an antecedent stimulus, a behavioural response, and then a consequence.

19
Q

Explain the related phenomena of temporal contiguity, generalisation, extinction and shaping.

A

temportal contiguity - having the conditioned and unconditioned stimulus close together, more effective at producing unconditioned response

generalisation - can transfer behaviour to other similar stimulus

extinction - gradual decrease in behaviour until its no longer produced, when behaviour no longer associated with consequences

shaping - desired behaviour broken down into simpler steps