Study for Midtterm 1 - 20pages Flashcards

1
Q

What is PHARMACOLOGY

A

Investigating the function-altering effect of exogenic and endogenic substances in living entities.

(can be produced e.g. insulin, thyroxin, adrenaline, noradrenalin etc.)

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2
Q

What is Pharmacodynamic?

A

How a drug acts on the body

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3
Q

What is Pharmacokinetics

A

How the body acts in response to a drug.

1- Absorption: How the drug enters the system and circulation i.e. does not apply when the drug is administered I/V.

2- Distribution: How drugs are dispersed in the tissues and fluids throughout the body.

3- Metabolism: How drugs are transformed throughout the body.

4- Excretion: Elimination of substances. In rare cases, some drugs irreversibly

accumulate in a tissue in the body.

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4
Q

Example of Pharmacodynamics and Pharmacokinetics

A

E.g. Magnesium Sulphate (MgSO4): Orally administered laxative.

Pharmacodynamics: The osmotic effect of the unabsorbed ions, when ingested with a large volume of water, produces copious watery diarrhea.

Pharmacokinetics: Faecal excretion is the primary route of sulfate elimination.

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5
Q

DRUG-RECEPTOR INTERACTIONS:

Name the different interactions

A
  1. Physical interaction=
  2. Biochemical interaction: – with or without receptors, the target for the drug (ligand) is almost always a protein e.g. enzyme, receptor, ion channel, transporter etc.
    - Without receptors
    - With receptors
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6
Q

Name some 1. Physical interaction type of drugs

A

1- Osmotic Diuretics:

2- Antacids:

3- Laxatives

4- Chelators:

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7
Q
  1. Physical interaction

Name a Osmotic Diuretics:

A

Mannitol

Crossing of biological membrane = NO (No absorbtion)

Administered= IV

Enters= Glomerulus via Fenestrated capsule

Cannot be = Reabsorbed by the KIDNEY

Excreeted= GLOMERULAR FILTRATION - Osmotic Diuresis

USE = Acute renal failure (urine production stops) = leads to SHOCK due to no blood supply

=

Glycol poisoning (antifreeze) and the animal can die from a build-up of toxic substances.

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8
Q
  1. Physical interaction

- Antacids:

A

Magnesium Hydroxide (MgSO4)

RENNIE.

Used = build-up of gastric acid —> hyperacidity.

It aids by neutralizing the pH of HCl (1-2 elevated to 4-5).

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9
Q
  1. Physical interaction

Name a Laxative

A

Magnesium Sulphate (MgSO4)

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10
Q
  1. Physical Interaction
    - Chelators:
A

Bind with metal ions —-> form stable, water-soluble complexes.

EDTA – Used for lead poisoning/overdose.

Deferoxamine: Used for iron overdose.

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11
Q
  1. Physical interactions

EDTA – Used for

A

Lead poisoning/overdose.

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12
Q
  1. Physical Interaction

Deferoxamine used for:

A

Used for iron overdose.

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13
Q

Name the Biochemical interaction Without receptors

A

Inhibition of enzymes:

  • DNA damage:
  • Transporters:
  • Transporters:
  • Proton-pump inhibitors: e.g. OMEPRAZOLE (NB).
  • Diuretics: FUROSEMIDE
  • Ion channels:
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14
Q

Name some enzymes inhibitors of enxymes whitought receptors

A

1. NSAIDs – e.g. LOXICAM. These inhibit the cyclooxygenase enzyme (COX) and therefore is used as an anti-inflammatory (NSAID = non-steroidal anti-inflammatory drug). Other examples include MELOXICAM, CARPROFEN, ASPIRIN.

2. ACE inhibitors – angiotensin-converting enzymes inhibited in the case of hypertension. Decrease blood pressure and aid in heart failure.

3. AChE inhibitors – acetylcholinesterase enzyme inhibited therefore prevents breakdown of acetylcholine – build-up of Ach helps in muscle activation and contraction.

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15
Q
A
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