bioRxivBiochemistryPreprint
Toxicity assessment of 3-O--17β-marsdenin isolated from Gongronema latifolium leaf on selected brain and kidney function indices in mice
Onyedika Gabriel AniiD, Oluwatobi Ayodeji Medayedupin, Aminat Abike Azeez, Gideon Ampoma Gyebi, Isaac Duah Boateng, Joseph Oluwatope Adebayo
Abstract
The safety of bioactive compounds, especially those isolated from medicinal plants, is a major concern for health authorities, pharmaceutical industries, and the public. Of recent, anti-tumor pregnane glycosides were isolated from Gongronema latifolium leaf, of which the toxicity of one, 3-O-[6-deoxy-3-O-methyl-{beta}-D-allopyranosyl-(1[->]4)-{beta}-D-oleandropyranosyl]-17{beta}-marsdenin (3DMAOM), has not been evaluated. This study, therefore, evaluated the effects of 3DMAOM on selected brain and kidney function indices in mice. Female Swiss albino mice were randomly administered 5% dimethyl sulphoxide and different doses of 3DMAOM (0.5, 1, 2, and 4 mg/kg body weight) for fourteen (14) days, and their blood, brains, and kidneys were collected for biochemical analysis. There was no significant alteration in the activities of alkaline phosphatase (ALP), acetylcholinesterase, creatine kinase, Na+/K+-ATPase, Ca2+/Mg2+-ATPase, and Mg2+-ATPase in the brain of the treated groups compared to control. Also, no significant changes in the activities of ALP, gamma-glutamyltransferase, Na+/K+-ATPase, Ca2+/Mg2+-ATPase, and Mg2+-ATPase in the kidney of the treated groups compared to control. The plasma concentrations of Na+, K+, Cl-, PO43-, creatinine, and urea of mice were not significantly altered at all doses of the 3DMAOM compared to controls. However, the plasma concentration of Ca2+ was significantly reduced (p<0.05) at all doses of the 3DMAOM, and the plasma concentration of uric acid was significantly reduced (p<0.05) at 2 mg/kg body weight of the 3DMAOM compared to controls. These findings suggest that 3DMAOM isolated from Gongronema latifolium leaf may not adversely affect brain function but may affect calcium ion homeostasis in subjects.
- organism: mouse
- assay: proteomics
- research focus: drug response / drug discovery
- approach: experimental assay
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