Drugs that inhibit the synthesis of cholesterol and triglycerides in the liver Flashcards

1
Q
  1. HMG-CoA reductase inhibitors.

1

A

А. Fungal lactones activated in the liver:
Lovastatin: reduces cholesterol by 30%, LDL by 39%.
Simvastatin: reduces cholesterol by 25-30%, LDL by 35-38%

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2
Q
  1. HMG-CoA reductase inhibitors. The most active hypocholesterolemic agents do not increase the TG level:
    (2)
A

B. Semisynthetic fungal lactone:

Pravastatin- reduces cholesterol by 20-25%, LDL by 25-30%

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3
Q
  1. HMG-CoA reductase inhibitors. The most active hypocholesterolemic agents do not increase the TG level:
    (3)
A

C. Synthetic indole derivatives:
Fluvastatin- - reduces cholesterol by 22-25%, LDL by 24-31%
Side effects : with combined use of statins and fibrates - reversible hepatitis, muscle pain, nausea, headache, sleep disorders
Indications: dyslipidemia, hypercholesterolemia and triglyceridemia

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4
Q

2) Nicotinic acid drugs

A

Nicotinic acid

Enduracin

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5
Q

Nicotinic acid

A

water-soluble
vitamin B group
LDL - by 15-30%, increases

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6
Q

Nicotinic acid Indications:

A

any atherogenic dyslipidemia

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7
Q

Nicotinic Side effects

A

(20%) irritation of the stomach, liver cells, redness and itching of the skin (correction - take 30 minutes 325 mg of aspirin)

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8
Q

Nicotinic Contraindications

A

diabetes, gout, peptic ulcer, hepatitis, cardiac arrhythmias

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9
Q

Enduracin

A

prolonged form of nicotinic acid
Well absorbed in the digestive tract
practically does not give adverse reactions
The effect develops after 1.5 months from the beginning of the reception, lasts 2 months after the termination of the reception

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10
Q
  1. Fibric acid derivatives (fibrates)
A

Indications: hypertriglyceridemia (dyslipidemia II B, III, IV
Side effects: stone formation in the biliary tract, muscle pain
Contraindications: liver disease, blood diseases (anemia, leukopenia)
Bezafibrat - reduces TG less effectively

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