Dibicor, tablets 500 mg 60 pcs

Dibicor is metabolic.

Pharmacodynamics

Taurine is a natural product of the metabolism of sulfur-containing amino acids: cysteine, cysteamine, methionine. Taurine has osmoregulatory and membrane-protective properties, has a positive effect on the phospholipid composition of cell membranes, and normalizes the exchange of calcium and potassium ions in cells.

Taurine showed properties of inhibitory neurotransmitter, it has anti-stressor effect, can regulate the release of GABA, adrenaline, prolactin and other hormones and regulate responses to them.

Participating in the synthesis of respiratory chain proteins in mitochondria, taurine regulates oxidative processes and exhibits antioxidant properties; it affects enzymes such as cytochromes responsible for the metabolism of various xenobiotics.

Dibicor® improves metabolic processes in the heart, liver and other organs and tissues.

In chronic diffuse liver diseases Dibicor® increases blood flow and reduces the severity of cytolysis. It reduces congestion in the small and large circulatory system: intracardiac diastolic pressure decreases, myocardial contractility increases (maximal contraction and relaxation rate, contractility and relaxation indices).

The drug moderately decreases BP in patients with arterial hypertension and has almost no effect on BP in patients with CVD with lowered BP.

Dibicor® decreases side effects of overdose of cardiac glycosides and slow calcium channel blockers; decreases hepatotoxicity of antifungal agents. Improves performance under heavy physical activity.

Dibicor® decreases blood sugar level in diabetics about 2 weeks after taking the drug. A significant reduction of triglycerides concentration and, to a lesser degree, of cholesterol level and atherogenicity of plasma lipids is also observed. Long-term use of the drug (about 6 months) showed improvement of the microcirculatory blood flow in the eye.

Pharmacokinetics

After a single use of 500 mg of Dibicor® the active substance (taurine) is determined in blood after 15-20 minutes, Cmax is reached after 1.5-2 hours. The drug is completely eliminated in 24 hours.