Drugs that inhibit the synthesis of cholesterol and triglycerides in the liver Flashcards
- HMG-CoA reductase inhibitors.
1
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%
- HMG-CoA reductase inhibitors. The most active hypocholesterolemic agents do not increase the TG level:
(2)
B. Semisynthetic fungal lactone:
Pravastatin- reduces cholesterol by 20-25%, LDL by 25-30%
- HMG-CoA reductase inhibitors. The most active hypocholesterolemic agents do not increase the TG level:
(3)
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
2) Nicotinic acid drugs
Nicotinic acid
Enduracin
Nicotinic acid
water-soluble
vitamin B group
LDL - by 15-30%, increases
Nicotinic acid Indications:
any atherogenic dyslipidemia
Nicotinic Side effects
(20%) irritation of the stomach, liver cells, redness and itching of the skin (correction - take 30 minutes 325 mg of aspirin)
Nicotinic Contraindications
diabetes, gout, peptic ulcer, hepatitis, cardiac arrhythmias
Enduracin
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
- Fibric acid derivatives (fibrates)
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