Lecture 2 - Drugs: What You Need To Know And Why Flashcards

1
Q

Define pharmacodynamics

A

What drugs do to the body

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2
Q

Define pharmacokinetics

A

What the body does to drugs

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3
Q

What are drug targets

A

Largely regulatory proteins, although can be exceptions (e.g. targeting of DNA by some anti tumour drugs)
Examples are: receptors, ion channels, enzymes, carrier molecules

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4
Q

How do drugs elicit a therapeutic effect?

A

Targeted interaction, normalisation and disease management

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5
Q

How do drugs elicit a desired effect?

A

The beneficial outcomes that drugs are intended to produce e.g. pain reliever ibuprofen reduces pain and inflammation

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6
Q

How do drugs elicit a adverse effect?

A

i.e. side effects - they are unintended and potentially harmful

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7
Q

How do drugs elicit a toxic effect?

A

occurs when a drug produces harmful effects often due to excessive dosage or accumulation in body

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8
Q

Describe the processes and phases in drug discovery and development

A

typically involves:
- Early Drug Discovery, Pre-Clinical Phase, Clinical Phases, and Regulatory Approval

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9
Q

types of receptors:

A

ligand-gated ion channels
G protein-coupled receptors
catalytic receptors
nuclear receptors

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10
Q

ligand-gated ion channels

A

Ligand binding induces conformational change allowing movement of ions through pore, rapid, e.g. nicotinic acetylcholine receptor

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11
Q

G protein-coupled receptors

A

Transmembrane proteins, receptor activation elicits a conformational changes causing cascade of reactions, intermediate, e.g. muscarinic acetylcholine receptor

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12
Q

catalytic receptors

A

Ligand binding leads to receptor dimerisation and phosphorylation of specific residues on receptor – alters the enzymatic activity of receptor, hours, e.g. growth factors

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13
Q

nuclear receptors

A

Ligand-activated transcription factors that can enhance or repress gene transcription, hours, e.g. steroid hormones

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14
Q

how can receptors work as amplifiers?

A

Secondary messengers are able to amplify signs and direct signals to specific cellular locations. Second messenger concentration and localisation need to be tightly regulated.

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