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Herbal extracts differentially inhibit oxidative effects caused by the biotransformation of nifurtimox, nitrofurantoin and acetaminophen on rat liver microsomes / Extractos herbales inhiben diferencialmente los efectos oxidativos causados por la biotransformación de nifurtimox, nitrofurantoína y acetaminofeno en microsomas hepáticos de rata]
Letelier, María E; Iturra-Montecinos, Pablo A; Gallardo-Garrido, Carlos A.
  • Letelier, María E; Universidad de Chile. Facultad de Ciencias Químicas y Farmacéuticas. Department of Pharmacological and Toxicological Chemistry. Laboratory of Pharmacology and Toxicology. Santiago. CL
  • Iturra-Montecinos, Pablo A; Universidad de Chile. Facultad de Ciencias Químicas y Farmacéuticas. Department of Pharmacological and Toxicological Chemistry. Laboratory of Pharmacology and Toxicology. Santiago. CL
  • Gallardo-Garrido, Carlos A; Universidad de Chile. Facultad de Ciencias Químicas y Farmacéuticas. Department of Pharmacological and Toxicological Chemistry. Laboratory of Pharmacology and Toxicology. Santiago. CL
Bol. latinoam. Caribe plantas med. aromát ; 16(2): 88-98, mar. 2017. tab, graf
Article in English | LILACS | ID: biblio-881315
ABSTRACT
Inflammation is a cellular defensive mechanism associated to oxidative stress. The administration of nitrofurantoin, nifurtimox and acetaminophen generates oxidative stress by their biotransformation through CYP450 system. The main adverse effect described for the first two drugs is gastrointestinal inflammation and that of the last, hepatitis. Therefore, standardised dry extracts from Rosmarinus officinalis, Buddleja globosa Hope, Cynara scolymus L., Echinacea purpurea and Hedera helix were tested to evaluate their capacity to decrease drug-induced oxidative stress. For that, rat liver microsomes were incubated with drugs in the presence of NADPH (specific CYP450 system cofactor) to test oxidative damage on microsomal lipids, thiols, and GST activity. All drugs tested induced oxidation of microsomal lipids and thiols, and inhibition of GST activity. Herbal extracts prevented these phenomena in different extension. These results show that antioxidant phytodrugs previously evaluated could alleviate drugs adverse effects associated to oxidative stress.
RESUMEN
Inflamación es un mecanismo de defensa el cual está asociado a estrés oxidativo. La administración de nitrofurantoína, nifurtimox y paracetamol genera estrés oxidativo al metabolizarse a través del sistema CYP450. El principal efecto adverso de los dos primeros fármacos es inflamación gastrointestinal y del tercero, hepatitis. Por lo tanto, utilizamos diversos extractos herbales para disminuir el estrés oxidativo inducido por estos fármacos. Para esto se incubaron microsomas hepáticos de rata con dichos fármacos en presencia de NADPH (cofactor específico del sistema CYP450) y se evaluó el daño oxidativo generado sobre los lípidos, los tioles y la actividad GST microsómica. Todos los fármacos indujeron oxidación de los lípidos y los tioles microsómicos e inhibieron la actividad GST. Los extractos herbales previnieron estos fenómenos oxidativos en diferente extensión. Estos resultados indican que fitofármacos antioxidantes previamente evaluados, podrían aliviar los efectos adversos asociados a estrés oxidativo de los fármacos.
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Full text: Available Index: LILACS (Americas) Main subject: Microsomes, Liver / Plant Extracts / Oxidative Stress / Antioxidants Limits: Animals Language: English Journal: Bol. latinoam. Caribe plantas med. aromát Journal subject: Botany / Medicine / Plantas Medicinais / Terapias Complementares Year: 2017 Type: Article Affiliation country: Chile Institution/Affiliation country: Universidad de Chile/CL

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Full text: Available Index: LILACS (Americas) Main subject: Microsomes, Liver / Plant Extracts / Oxidative Stress / Antioxidants Limits: Animals Language: English Journal: Bol. latinoam. Caribe plantas med. aromát Journal subject: Botany / Medicine / Plantas Medicinais / Terapias Complementares Year: 2017 Type: Article Affiliation country: Chile Institution/Affiliation country: Universidad de Chile/CL