Subacute and subchronic oral toxicity assessments of Acridocarpus smeathmannii (DC.) Guill. & Perr. root in Wistar rats

• Published in: Toxicology reports Vol. 6; pp. 161 - 175
• Main Authors: Kale, O.E., Awodele, O., Akindele, A.J.
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 01.01.2019; Elsevier
• Subjects: Acridocarpus smeathmannii (DC.) root; Safety study; Subacute toxicity; Subchronic toxicity; Toxicology; Wistar rats; COX-2; Subchronic toxicity; Wistar rats; Subacute toxicity; Toxicology; HEASR; Acridocarpus smeathmannii (DC.) root; ROS; Safety study; HEASR4; FSH; HEASR5; HEASR6; ELISA; HEASR4, 250 mg/kg ofhydroethanolic extract of A. Smeathmannii (DC.) root; COX-2, cyclooxygenase-2; HEASR5, 500 mg/kg ofhydroethanolic extract of A. Smeathmannii (DC.) root; HEASR6, 1000 mg/kg ofhydroethanolic extract of A. Smeathmannii (DC.) root; HEASR, hydroethanolic extract of A. Smeathmannii (DC.) root; ELISA, enzyme-linked immunosorbent assay; FSH, Follicle stimulating hormone; ROS, reactive oxygen species
• ISSN: 2214-7500; 2214-7500
• DOI: 10.1016/j.toxrep.2019.01.005

[Display omitted] Recent adverse herb reactions have stimulated interest documenting the safety profile of medicinal agents. Thus, subacute and subchronic oral toxicity of the hydroethanolic extract of Acridocarpus smeathmannii root (HEASR) in Wistar rats was investigated. In the 28 and 90-day subacute and subchronic toxicity tests, sixty-four rats (n = male: female = 1:1 = 32) were divided into four of eight/group and ninety-six (n = male: female = 1:1 = 48) into twelve/group respectively. Distilled water (10 mL/kg) or HEASR4, HEASR5 and HEASR6 (250, 500 and 1000 mg/kg/day) respectively were administered via oral gavage. Animals were killed humanely 24 h after the last administration. Using standard methods, acute oral toxicity dose of HEAR (2000 mg/kg) was non-lethal in rodents. Subacute administration of HEASR6 increased total bilirubin (p < 0.05) in female rats. HEASR moderately altered both haematological and biochemical indices in rats. HEASR6 administration reduced ovary weight in both studies while follicle stimulating hormone level in male was reduced at all doses used. HEASR modulated lipid peroxidation, sperm quality and elevated cyclooxygenase-2 levels in rats. Histology revealed gastritis and congestions in vital organs. The low-observed adverse effect level for HEASR was below 250 mg/kg for both sexes. Overall, HEASR demonstrated inherent toxicity evidenced by our current findings. The exaggeration of its folklore medicine applications calls for cautions.