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DOI 10.1016/j.clinbiochem.2015.04.017

Медицинская библиотека · Clinical biochemistry · 2015

A review on the possible molecular mechanism of action of N-acetylcysteine against insulin resistance and type-2 diabetes development.

Lasram Mohamed Montassar, Dhouib Ines Bini, Annabi Alya, El Fazaa Saloua, Gharbi Najoua

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Аннотация

OBJECTIVE

N-acetylcysteine (NAC), a cysteine pro-drug and glutathione precursor has been used in therapeutic practices for several decades, as a mucolytic agent and for the treatment of numerous disorders including paracetamol intoxication. There is a growing interest concerning the beneficial effects of NAC against the early stages of type-2 diabetes development. Nevertheless, the mechanisms underlying the therapeutic and clinical applications of NAC are not fully understood. In this review we aimed to focus on the protective effects of NAC against insulin resistance.

DESIGN AND

METHODS

The possible mechanisms of action were reviewed using the major findings of more than 100 papers relating to the antioxidant, anti-inflammatory and anti-apoptotic properties of NAC.

RESULTS

The anti-oxidative activity of NAC has been attributed to its fast reactions with free radicals as well as the restitution of reduced glutathione. Further, NAC has anti-inflammatory and anti-apoptotic properties which can have positive effects during the inflammatory process in insulin resistance. Moreover, NAC can modulate certain signaling pathways in both insulin target cells and β cells.

CONCLUSIONS

The diverse biological effects of NAC may make it a potential adjuvant or therapeutic target in the treatment of type-2 diabetes. So, further studies are required for determining its ability to alleviate insulin resistance and to improve insulin sensitivity.

Для цитирования: Lasram Mohamed Montassar, Dhouib Ines Bini, Annabi Alya, El Fazaa Saloua, Gharbi Najoua. A review on the possible molecular mechanism of action of N-acetylcysteine against insulin resistance and type-2 diabetes development.. Clinical biochemistry. 2015. DOI: 10.1016/j.clinbiochem.2015.04.017.

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