Clinical and pharmacological group: & nbsp

Glucocorticosteroids

Anticoagulants

Included in the formulation
  • Skinlight®
    cream externally 
    NIZHFARM, JSC     Russia
  • АТХ:

    D.07.X.C.03   Mometasone in combination with other drugs

    Pharmacodynamics:

    The drug interacts with the intentricular receptors of glucocorticoids, facilitating the release of the receptor from binding to immunophilin and heat shock proteins 70 and 90. Penetration of the activated receptor into the nucleus, binding to glucocorticoid-sensitive regulatory elements of DNA - a specific effect on gene expression (activation and suppression). Interaction with other protein transcription factors, including NFκB and AP-1, regulating the expression of many proteins of the immune system, which leads to suppression of the expression of genes encoding some cytokines, collagenase and stromelysins.

    The anti-inflammatory effect of mometasone is due to several factors.

    1. The drug induces the synthesis of lipocortin, which inhibits the activity of phospholipase A2. Inhibition of phospholipase-mediated A2 hydrolysis of membrane phospholipids of damaged tissues prevents the formation of arachidonic acid. The disruption of the formation of arachidonic acid actually means inhibition of the synthesis of prostaglandins, since arachidonic acid is a substrate for further metabolism along the cyclooxygenase pathway,and also on the lipoxygenase pathway with the corresponding inhibition of leukotriene synthesis.

    2. The anti-inflammatory effect of glucocorticoids is potentiated by their ability to inhibit the expression of COX-2 genes, which also leads to a decrease in the synthesis of prostaglandins in the inflammatory focus, including pro-inflammatory prostaglandins E2 and I2.

    3. Mometasone inhibits the expression of molecules of intercellular adhesion in the endothelium of blood vessels, violating the penetration of neutrophils and monocytes into the focus of inflammation. After the introduction of glucocorticoids, an increase in the concentration of neutrophils in the blood (due to their entry from the bone marrow and the restriction of migration from the blood vessels) is noted. This causes a decrease in the number of neutrophils in the site of inflammation.

    Mometasone inhibits the transcription of cytokine genes that stimulate the inflammatory and immune response (IL-1, IL-2, IL-6, IL-8), as well as tumor necrosis factor (and some others). Also note the reduction in velocity and increased transcription of genes degradation receptors to IL-1 and IL-2, inhibition of gene transcription metalloproteinases (collagenases, elastase and others) involved in the increase permeability of the vascular wall, in the processes of scarring and destruction of cartilaginous tissue in diseases of the joints.

    Immunosuppressive action is due to inhibition of transcription of DNA encoding the main histocompatibility complex, pro-inflammatory cytokines and inhibition of proliferation of T lymphocytes. It leads to a decrease in the number of T-lymphocytes and their influence on B-lymphocytes, inhibits the production of immunoglobulins. Reduces the formation and increases the decomposition of components of the complement system.

    The antiallergic effect is associated with the inhibition of the synthesis of mediators of allergy, degranulation of mast cells and release of mediators of allergy, and therefore it is effective for allergic reactions of immediate type.

    Heparin is an anticoagulant of direct action and has an antiproliferative, analgesic, anti-edematous and anti-inflammatory effect.

    Heparin acts on the factors of blood coagulation only after formation complex with endogenous anticoagulant antithrombin III. The main effect of the heparin-antithrombin III complex is directed against thrombin and factor Xa, however, the mechanisms of inhibition of these factors have some differences.To inactivate thrombin, it is necessary that heparin binds both to the molecule of antithrombin III and to the molecule of thrombin (heparin in this case serves as a matrix on which the formation of a covalent complex of thrombin with its inhibitor takes place). At the same time, for rapid inactivation of the factor Xa, there is no need for its binding to heparin (quite enough the heparin-induced change in the conformation of the active center of antithrombin III). Inhibition of thrombin (IIa factor) leads to inhibition of the transition of fibrinogen to fibrin.

    Pharmacokinetics:

    Mometasone is absorbed from the skin surface by 0.4%, with mucus by inhalation - less than 0.1%. The connection with plasma proteins is 98-99%, metabolized in the liver, excreted by the kidneys. The half-life is 5.8 h for mometasone.

    An insignificant amount of heparin is absorbed from the surface of the skin into the systemic circulation. The maximum concentration of heparin in the blood is noted 8 hours after the application. The elimination of heparin, mainly occurs through the kidneys, half-life of 12 hours.

    Indications:

    Psoriasis.

    Burns of 1 degree.

    Itching dermatoses.

    Insect bites.

    Sun burns.

    Discoid lupus erythematosus.

    Red flat lichen.

    Eczema.

    Atopic dermatitis.

    Simple chronic lichen (limited neurodermatitis).

    XII.L20-L30.L20.8   Other atopic dermatitis

    XII.L20-L30.L23   Allergic contact dermatitis

    XII.L20-L30.L24   Simple irritant contact dermatitis

    XII.L20-L30.L28.0   Simple chronic lichen

    XII.L20-L30.L29   Itching

    XII.L40-L45.L40   Psoriasis

    XII.L40-L45.L43   Lichen red flat

    XII.L50-L54.L50   Hives

    XII.L55-L59.L55   Sunburn

    XII.L80-L99.L93.0   Discoid lupus erythematosus

    XIX.T20-T32.T30   Thermal and chemical burns, unspecified

    Contraindications:

    Pregnancy.

    Tuberculosis.

    Syphilis.

    Breastfeeding period.

    Bacterial, fungal, viral skin infection.

    Pink acne.

    Perioral dermatitis.

    Age to 18 years.

    Post-vaccination reactions.

    Carefully:

    Application of occlusive dressings.

    The use of the drug on large areas of the skin for a long time.

    Application of the preparation on the face skin / intertriginous skin surface.

    Long-term use of glucocorticosteroids of systemic action.

    Pregnancy and lactation:

    Category FDA - C. Security drug for pregnant women and breast-feeding women was not investigated. It is known that glucocorticosteroids penetrate the placenta and are excreted in breast milk,in connection with which the use of glucocorticoid-containing drugs in pregnancy / breast-feeding is permissible only when absolutely necessary.

    Dosing and Administration:

    External topical application once a day, the course of treatment is from 7 to 28 days. In the treatment of limited vulgar psoriasis treatment is 21 days.

    Side effects:

    Side effects of glucocorticoids (including Cushing's syndrome).

    Local reactions: burning, itching, folliculitis, paresthesia, acne, atrophy, skin maceration, secondary infection, allergic dermatitis, hypopigmentation.

    Overdose:

    Secondary adrenal insufficiency, decreased function of the hypothalamic-pituitary-adrenal system.

    Treatment is symptomatic.

    Interaction:

    Not described.

    Special instructions:

    The drug can change the clinical manifestations of certain skin diseases, which can complicate the diagnosis.

    During the administration of the drug, adrenal function control is necessary.

    Impact on the ability to drive vehicles and manage mechanisms

    Does not affect the ability to manage transport and perform work that requires concentration.

    Instructions
    Up