Physiology Flashcards

1
Q

What is the cell membrane made of?

A

Lipids and proteins

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2
Q

Phospholipids make up most lipids in the cell membranes. How are they arranged?

A

Double layer: hydrophilic end (water soluble) faces out and in. Hydrophobic ends face internally

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3
Q

What is the name of the process by which mitochondrial make ATP (energy-rich compound)?

A

Oxidative phosphorylation

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4
Q

Where are the enzymes in mitochondria?

A

The mitochondrial has an outer membrane and inner membrane which is folded to form cristae (shelves) and the enzyme complexes responsible for oxidative phosphorylation line up on the cristae.

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5
Q

Where did mitochondria come from?

A

Aerobic bacteria

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6
Q

Do mitochondria have their own DNA?

A

Yes, double stranded molecule with 16500 base pairs - they have their own genome. Most proteins in the mitochondria are from nuclear genes, but mitochondrial DNA is responsible for some key parts of oxidative phosphorylation - thus mutations in nuclear DNA or mitochondrial DNA can lead to mitochondrial diseases

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7
Q

How many base pairs in nuclear DNA?

A

Over a billion

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8
Q

Where is zygote mitochondria derived from?

A

The ovum - thus inheritance is maternal

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9
Q

Is mitochondria DNA mutation rate higher or lower than nuclear DNA?

A

10 times higher. Ineffective DNA repair system

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10
Q

Is the interior of lysosomes more acidic or basic than the cytoplasm and why?

A

More acidic. So that if enzymes spill into cytoplasm, they aren’t as active ie it isn’t their favourite environment so they don’t digest things in the cytoplasm of the cell

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11
Q

What do lysosomes do?

A

Contain hydrolytic enzymes. Digest endocystosed bacteria and worn-out cell components

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12
Q

What happens when lysosomal enzymes are congenitally absent? ie lysosomal storage diseases

A

The lysosomes become engorged with the material that the enzyme normally degrades

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13
Q

What lysosomal enzymes is missing in: Fabry disease, gaucher disease and Tay-Sachs disease?

A

Fabry disease: alpha-galactosidase
Gaucher disease: beta-galactocerebrosidase
Tay-Sachs disease: hexosaminidase A

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14
Q

What happens in Tay-Sachs disease?

A

Loss of enzyme that breaks down gangliosides (fatty acids derivatives) - mental retardation and blindness

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15
Q

What are microtubules?

A

Part of the cells cytoskeleton - the tracks for organelles to move around the cell, and also form the spindle, which moves the chromosomes in mitosis

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16
Q

What is a medication disrupting microtubules? ie in oncology medications so that mitotic spindles can’t form and cells die

A

Vincristine

Colchacine