Alimentary - metabolism Flashcards

1
Q

What is catabolic?

A

Breaks molecules down

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2
Q

What is anabolic?

A

Joins molecules together

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3
Q

What is Gibbs free energy?

A

A value that defines how spontaneous a reaction is, with a negative value meaning the reaction is spontaneous, and a positive value meaning the reaction is non-spontaneous.

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4
Q

What is the equation for Gibbs free energy?

A

G = H-TS OR G=G products - G reactants

H = heat
T - absolute temp
S - absolute entrophy

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5
Q

What are the two main components that decide if a reaction is spontaneous or not?

A

Inherent free energy change (must be negative)

Mass action

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6
Q

What is mass action?

A

Concentration of products v reactants. More products means G increases, making it less likely to occur

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7
Q

What is ATP?

A

An energy transducer, generated from catabolic reactions. The phosphate bonds contain energy

Break off one or two that can give ATP, ADP or AMP

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8
Q

What is an enzyme?

A

Protein that speeds up a reaction by lowering activation energy (not changing Gibbs) by binding to a side modifying the substrate

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9
Q

What is the lock and key model?

A

The enzyme is sympathetic to the substrate and fit without change

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10
Q

What is the induced fit model?

A

Presence of an enzyme or another substrate lead to changing the shape of the active site, allowing them to fit together.

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11
Q

What is an allosteric substrate?

A

The additional substrate that can change the conformation of the protein binding to it, e.g. Hb and binding of O2 allows more O2

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12
Q

What are the three tiers of metabolic control?

A

Mass action affects free energy

Enzymes are controlled by:
-One rate controlling enzyme
- Amount of enzyme + activity level (allosterically and/or by reversible covalent modification controlled hormones)
-Direction of pathway set by irreversible actions

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13
Q

What is gylcolysis?

A

Conversion of glucose to energy, without O2 (anerobic and aerobic)

Occurs in all tissues, but primarily the liver and muscles.

Can enter through glucose, glucogenolysis and other monosaccharides

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14
Q

What occurs in glycolysis?

A

Blood glucose
Hexokinase | (irreversible) ADP
G-6-P
|
F-6-P
PFK | (irreversible) ADP
F-1,6-P
|
| 2xATP and 2xNADH+H+
|
2x PEP
Pyruvate kinase | 2xATP
2x Pyruvate
| (irreversible) CO2 and NADH + H+
Acetyl CoA

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15
Q

What is the citric acid cycle?

A

Acetyl CoA is used into the citric acid cycle. It creates most of the ATP.

Citrate goes to alpha ketogenesis and to OAA.

Output is 2xCO2, 3xNADH, 3x H+, FADH2 and GTP

The NADH produced goes to electron transport chain.

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16
Q

What is the electron transport chain?

A

Operates under aerobic conditions, requires a supply of NAD+ and FAD.

In mitochondria wall, with 5 carrier protein complexes. As the electrons pass into the complexes, energy is created to pump H+ in to the intramembranous space creating a protein motive force.

This then re-enters the matrix via ATP synthase creating ATP (most of it)

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17
Q

What disrupts the ECT?

A

Uncoupling agents, provide alternative routes for protons to pass into the matrix, without going through ATP synthase. Less ATP is created but does create heat.

18
Q

What happens in anaerobic respiration?

A

No O2 = no ETC.

Excessive NADH and pyruvate.

Pyruvate is converted to lactate which is converted back to pyruvate (in liver ) by NADH allowing glycolysis to continue

19
Q

How is carbohydrate stored?

A

Glyogenesis - excess glucose is converted to glycogen which is stored in liver by glycogen synthase.

20
Q

What is glycogenolysis?

A

When theres a demand for glucose, glycogen broken down by glycogen phosphorylase.

Occurs in liver and muscle (in situ use)

21
Q

what is allosteric regulation of glycogenesis/glucogenolysis?

A

G6P upregulates glycogen synthase

ATP and glucose inhibits glycogen phosphorylase

22
Q

What is hormonal regulation of glycogensis/glucogenolysis?

A

Glucagon and noradrenaline/adrenaline up regulate adenylate cyclase

and activate glycogen phosphorylase

23
Q

How are lipids metabolised?

A

TAGs are stored

Lipolysis - uses fat storage

Lipogenesis - creates fat storage

24
Q

How does lipolysis work?

A

Tags hydrolysed into FA and glycerol by triglyceride lipase

FA bind to albumin, making them insoluble transported to tissues and liver

Enter the hepatocytes and converted to glycerol-3-phosphate entering glycolysis
and the FA undergoes beta oxidation in mitochondria

25
What promotes lipolysis?
Glucagon and adrenaline
26
What inhibits lipolysis?
Insulin
27
What is ketogenesis?
Large amounts of beta oxidation occur in liver but only small amount used for energy. Excess Acetyl CoA converted into acids + acetone (ketone bodies)
28
What is lipogenesis?
FA are combined to form TAG.
29
What inhibits lipogenesis?
Glucagon and adrenaline
30
What stimulates lipogenesis?
Insulin
31
What is gluconeogenesis?
Formation of glucose from non-carb sources occurs after 8 hours of fasting, when glycogen stores deplete or an alternative source of glucose is required. Happens in liver and in cortex of kidney Uses 6 ATP
32
What are the non-carb sources of gluconeogenesis?
Lactate from anerobic glycolysis Glycerol from TAGs Glucogenic amino acids RBCs via cori cycle
33
What is the hormonal control of gluconeogenesis?
Glucagon and cortisol up regulate the enzymes in a high
34
What are the liver proteins?
Albumin, Globulin, Fibrinogen, CRP, Clotting factors, Thrombopoietin, Angiotensinogen and Amino acids
35
Once cells reach their limit on protein storage, rest of amino acids are metabolised in liver by...
Transamination - AA -> Keto-acids Deamination - glutamate is metabolised further
36
What is the urea cycle?
Removes ammonium, and remakes alpha ketoglutarate for use.
37
What happens if there are issues with the urea cycle?
Ammonia rises, reversing the reaction of glutamate which builds up causing nervous system issues (is a neurotransmitter)
38
Clinical signs of ammonia toxicity?
Intolerance of high protein food Vomitin Metal retardation Coma/death
39
What is GLUT1+3?
Always on cells, basal slow uptake and feeds all cells working
40
What is GLUT 5?
A receptor on the SI for absorption
41
What is GLUT2?
In pancreatic beta cells and hepatocytes, works usually in hyperglycaemia
42
What is GLUT 4?
In muscles and adipocytes, working at baseline glucose level. Needs internalised transporters within cells and insulin stimulates this.