Epirubicin Treatment Induces Neurobehavioral, Oxido-Inflammatory and Neurohistology Alterations in Rats: Protective Effect of the Endogenous Metabolite of Tryptophan − 3-Indolepropionic Acid

• Published in: Neurochemical research Vol. 48; no. 9; pp. 2767 - 2783
• Main Authors: Owumi, Solomon E., Adebisi, Grace
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.09.2023; Springer Nature B.V
• Subjects: Antioxidants; Biochemistry; Biocompatibility; Biomarkers; Biomedical and Life Sciences; Biomedicine; Body weight; Breast cancer; Cell Biology; Cerebellum; Cerebrum; Chemotherapy; Cognitive ability; Damage assessment; DNA damage; Epirubicin; Histopathology; Inflammation; Lipid peroxidation; Lipids; Metabolism; Metabolites; Neurochemistry; Neurology; Neurosciences; Neurotoxicity; Nitric oxide; Original Paper; Oxidants; Oxidative stress; Oxidizing agents; Peroxidase; Peroxidation; Reactive nitrogen species; Reactive oxygen species; Toxicity; Tryptophan; Xanthine oxidase; Oxidative stress pro-inflammatory response; 3-Indolepropionic acid; Neurotoxicity; Epirubicin; Antioxidant booster
• ISSN: 0364-3190; 1573-6903
• DOI: 10.1007/s11064-023-03941-9

Epirubicin’s (EPI) efficacy as a chemotherapeutic agent against breast cancer is limited by EPI’s neurotoxicity associated with increased oxidative and inflammatory stressors. 3-Indolepropionic acid (3-IPA) derived from in vivo metabolism of tryptophan is reported to possess antioxidative properties devoid of pro-oxidant activity. In this regard, we investigated the effect of 3-IPA on EPI-mediated neurotoxicity in forty female rats (180–200 g; five cohorts (n = 6) treated as follows: Untreated control ; EPI alone (2.5 mg/Kg); 3-IPA alone (40 mg/Kg body weight); EPI (2.5 mg/Kg )  +  3-IPA (20 mg/Kg) and EPI (2.5 mg/Kg ) + 3-IPA (40 mg/Kg) for 28 days. Experimental rats were treated with EPI via intraperitoneal injection thrice weekly or co-treated with 3-IPA daily by gavage . Subsequently, the rat’s locomotor activities were measured as endpoints of neurobehavioural status. After sacrifice, inflammation, oxidative stress and DNA damage biomarkers were assessed in rats’ cerebrum and cerebellum alongside histopathology. Our results demonstrated that locomotor and exploratory deficits were pronounced in EPI-alone treated rats and improved in the presence of 3-IPA co-treatment. EPI-mediated decreases in tissue antioxidant status, increases in reactive oxygen and nitrogen species (RONS), as well as in lipid peroxidation (LPO) and xanthine oxidase (XO) were lessened in the cerebrum and cerebellum of 3-IPA co-treated rats. Increases in nitric oxide (NO) and 8-hydroxydeguanosin (8-OHdG) levels and myeloperoxidase MPO activity were also abated by 3-IPA. Light microscopic examination of the cerebrum and cerebellum revealed EPI-precipitated histopathological lesions were subsequently alleviated in rats co-treated with 3-IPA. Our findings demonstrate that supplementing endogenously derived 3-IPA from tryptophan metabolism enhances tissue antioxidant status, protects against EPI-mediated neuronal toxicity, and improves neurobehavioural and cognitive levels in experimental rats. These findings may benefit breast cancer patients undergoing Epirubicin chemotherapy.