Abstract

Metronidazole (MTZ) and Cotrimoxazole (CTX) are used in HIV/AIDS patients eligible for antiretroviral treatment. The objective of this animal study was to determine whether pre-treatment with antibiotics affects the intestinal bioavailability of Atazanavir (ATV) and Ritonavir (RTV). After oral administration of 1 mg MTZ and CTX for 7 days, the rat colonic mucosa were analyzed for mucus thickness or placed in Ussing chambers to measure ATV and RTV net transepithelial fluxes (Jnet). 1. In control rats, the mucus thickness was 43.3±7.6 µm and 40.7±6.9 µm, in proximal and distal colon, respectively. In proximal colon, the thickness was 57.2±8.8 and 58.2±6.9 µm after MTZ and CTX, respectively whereas in distal colon, the thickness was 121.1±38.4 and 170.5±35.0 µm (P<0.05) respectively. 2. Transepithelial conductance was reduced after MTZ or CTX in the proximal and distal colon. 3. In control, net ATV secretion was observed both in proximal (−0.36±0.02 µg.hr−1 cm−2) and distal colon (−0.30±0.08 µg.hr−1 cm−2). After MTZ and CTX, it was increased in the proximal colon by two 2 fold and 4 fold, respectively and in the distal colon by 3 fold and 5 fold, respectively. 4. In control, there was no net active RTV transport either in proximal (+0.01±0.01 µg.hr−1 cm−2) or distal colon (+0.04±0.01 µg.hr−1 cm−2). After MTZ and CTX, secretion was increased 5 fold and 10 fold, respectively, in the proximal colon and two fold and 5 fold, respectively in the distal colon (p<0.001). In conclusion, after MTZ and CTX therapy, the mucus layer was enlarged, passive permeability was decreased and ATV and RTV were actively secreted by the colonic epithelium suggesting that, in rat, the intestinal bioavailability of ATV and RTV is impaired after antibiotic therapy.

Highlights

  • Atazanavir (ATV) is an azapeptide HIV-1 protease inhibitor (PI) and one of the antiretrovirals (ARV) used in second-line therapy in adults and adolescents with HIV infection according to the recommendations for a public heath approach of the World Health Organization (WHO)’s 2010 guidelines

  • After MTZ and CTX therapy, the mucus layer was enlarged, passive permeability was decreased and ATV and RTV were actively secreted by the colonic epithelium suggesting that, in rat, the intestinal bioavailability of ATV and RTV is impaired after antibiotic therapy

  • Mucus Thickness (MT) Pre-treatment of animals with antibiotics resulted in an increase in intestinal thickness of mucus in proximal and distal colon

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Summary

Introduction

Atazanavir (ATV) is an azapeptide HIV-1 protease inhibitor (PI) and one of the antiretrovirals (ARV) used in second-line therapy in adults and adolescents with HIV infection according to the recommendations for a public heath approach of the World Health Organization (WHO)’s 2010 guidelines. Metronidazole (MTZ) and Cotrimoxazole (CTX) are two antibiotics commonly used in HIV/AIDS patients; in particular, in those with baseline CD4 counts close to that of patients eligible for antiretroviral treatment. CTX remains popular due to its low cost, effectiveness and familiarity among clinicians. It is the most common antibiotic prescribed to patients with urinary tract infections [3]. Low-dose CTX is commonly used for prophylaxis against opportunistic Pj and Tg infections [4] among patients with depressed CD4 counts. A recent study showed that MTZ therapy is associated with an increase of luminal mucus thickness in rats [5] pointing to a potential deleterious effect on the drug’s intestinal bioavailability

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