Erdosteine Therapy for Renal Failure: Current Perspectives

I read the recently published paper of Ebru Uz et al. (1), in the Nephro-Urology Monthly which focused on the renoprotective effects of erdosteine when it is used for cyclosporine-A (CsA) induced chronic nephrotoxicity. Erdosteine belongs to the class of mucolytics which is used for the treatment of wet cough and chronic obstructive pulmonary disease (CoPD). It has been reported that erdosteine possesses multiple mechanisms to protect against hepatic, renal, retinal and cardiotoxicity (2, 3). Erdosteine is a prodrug and metabolite I is the active metabolite of erdosteine owing to its free thiol group. It modifies the clinical outcome by improving the symptoms and reducing the progress of the disease. Pharma-cokinetics of erdosteine results in rapid absorption after oral administration; distribution with protein binding is 64.5%; first pass metabolism to form an active metabolite i.e., N-thiodiglycolyl-homocysteine t 1/2 4.6 hour in rats; ex-cretion through urine as metabolites, elimination half-life approximately 1.46 hr (erdosteine), and about 1.62 hr (metabolite). Common adverse reactions/side effects are epigastralgia, nausea, vomiting, diarrhea, spasmodic colitis, taste alteration, urticaria, eczema, erythema and headaches (4). Contraindications are, caution to be used during pregnancy and lactation. Erdosteine contains two sulfhydryl groups and it is reported that in the pharma-codynamics it breaks the disulphide bonds, which hold the glycoprotein fibers of mucus together. Furthermore, it makes the secretions and mucous more fluid which enhances elimination (5). CsA is an immunosuppressant drug widely used in post-allogeneic organ transplants to reduce the activity of the immune system, and therefore it lessens the risk of organ rejection. CsA, was initially isolated from the fungus Tolypocladium inflatum and extracted from a soil sample, this was obtained by Sandoz scientists at hardangervid-da, Norway in 1969 (6). however, CsA is a very lipophilic agent, and this facilitates attachment to cellular membranes leading to lipid degradation and peroxidation with further release of free radicals and oxidative stress which may result in CsA-resistance and nephrotic syndrome (1, 7). I agree with Ebru Uz et al. that erdosteine may protect renal tissue by alteration of CsA induced rising oxidative stress markers i.e., glutathione peroxidase, cata-lase, malondialdehyde and nitric oxide levels along with histopathological changes (1). Furthermore, erdosteine may improve several toxic drug side effects such as those