Isoniazid metabolism and hepatotoxicity

Acta Pharm Sin B. 2016 Sep;6(5):384-392. doi: 10.1016/j.apsb.2016.07.014. Epub 2016 Aug 3.

Abstract

Isoniazid (INH) is highly effective for the management of tuberculosis. However, it can cause liver injury and even liver failure. INH metabolism has been thought to be associated with INH-induced liver injury. This review summarized the metabolic pathways of INH and discussed their associations with INH-induced liver injury.

Keywords: ALP, alkaline phosphatase; ALT, alanine aminotransferase; AcHz, acetylhydrazine; AcINH, acetylisoniazid; Amidase; Anti-tuberculosis; DiAcHz, diacetylhydrazine; GSH, glutathione; GST, glutathione S-transferase; Hepatotoxicity; Hz, hydrazine; INA, isonicotinic acid; INH, isoniazid; Isoniazid; MPO, myeloperoxidase; Metabolism; N-Acetyltransferase 2; NAD+, nicotinamide adenine dinucleotide; NAT, N-acetyltransferase; P450, cytochrome P450; R.M., reactive metabolite; TB, tuberculosis.

Publication types

  • Review