Tranilast: A novel weapon against insulin resistance

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Summary

Oxidative stress and inflammatory cytokines such as monocyte chemoattractant protein 1 (MCP-1), TGF-β, and IL-2 are supposed to play crucial roles in the pathogenesis of insulin resistance (IR).

Tranilast is an anti-allergic drug which exerts anti-inflammatory and anti-angiogenesis effects through inhibition of expression of MCP-1, TGF-β, and antigen-induced IL-2 lymphocyte responsiveness. It also possesses a certain antioxidant activity.

Considering the above facts and in view of its safety, tranilast may prove invaluable in the treatment of IR.

Section snippets

Overview of the pathomechanism behind insulin resistance (IR)

IR contributes to a number of metabolic disorders including type 2 diabetes, hypertension and atherosclerosis, and has been characterized as an inflammatory disease [1], [2]. Inflammatory markers such as tumor necrosis factor-alpha (TNF-α), transforming growth factor-beta (TGF-β), interleukin (IL)-1β, IL-2, IL-6, plasminogen activator inhibitor 1 (PAI-1) and monocyte chemoattractant protein-1 (MCP-1) have been reported to be present in higher concentrations in IR people than in normal people [2]

Phamacodynamic effects of tranilast relating to the proposal

Tranilast, N-(3,4-demethoxycinnamyl)-anthranilic acid, is an anti-allergic agent used mainly to treat allergic diseases such as atopic dermatitis, bronchial asthma and allergic rhinitis. The drug exhibits its therapeutic effect in these conditions by inhibiting the release of chemical mediators from mast cells and basophils [11]. This agent is also used to prevent keloid formation after skin injury by reducing collagen synthesis in keloid cells through interference with TGF-β effects [12].

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