Details

Autor(en) / Beteiligte

• Pondugula, Satyanarayana R.
• Salamat, Julia M.
• Abbott, Kodye L.
• Flannery, Patrick C.
• Majrashi, Mohammed
• Almaghrabi, Mohammed
• Govindarajulu, Manoj
• Ramesh, Sindhu
• Onteru, Suneel K.
• Sandey, Maninder
• Haung, Chen-Che J.
• Gill, Kristina
• Narayanan, Natasha
• McElroy, Edwin
• Desai, Darshini
• Nadar, Rishi
• Moore, Timothy
• Kalyanam, Nagabhushanam
• Majeed, Muhammed
• Dhanasekaran, Muralikrishnan

Titel

Oroxylum indicum Extract, at a Physiologically Relevant Dosage, Does Not Induce Hepatotoxicity in C57BL/6J Mice

Ist Teil von

• Natural product communications, 2021-05, Vol.16 (5), p.1934578

Ort / Verlag

Los Angeles, CA: SAGE Publications

Erscheinungsjahr

2021

Link zum Volltext

Quelle

EZB Electronic Journals Library

Beschreibungen/Notizen

• Background Botanical supplements have been proven to provide beneficial health effects. However, they can induce unintended adverse events such as hepatotoxicity. Oroxylum indicum extract (OIE, Sabroxy®) has several health benefits including anti-inflammatory, anti-arthritic, antifungal, antibacterial, and neuroprotective effects. It is currently unknown whether OIE has the potential to induce hepatotoxicity. Purpose In the current study, we sought to determine whether OIE can induce hepatotoxicity in C57BL/6J mouse model. Methods The male mice were fed powdered rodent food (control group) or powdered rodent food mixed with OIE (Sabroxy®, 500 mg/kg) daily for 4 weeks. Following the treatment, we assessed liver histology and serum levels of biomarkers commonly associated with liver damage, including alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP). Results No significant alterations were observed in liver histology, and serum levels of ALT, AST, ALP, bilirubin, albumin, globulin, and total protein in the OIE fed mice compared to the control mice. Conclusion Taken together, our results suggest that OIE, when fed at its physiologically relevant dosage, does not induce hepatotoxicity in C57BL/6J mice.