Infectious Diseases and Herbal Medicine (Sep 2022)

Behavioural studies on crude Ethanol leaf extract of Cadaba farinosa Forssk. in mice

  • Muhammad Awwal Tijjani,
  • Mohammed Garba Magaji,
  • Abdullahi Hamza Yaro,
  • Hamidu Usman,
  • Aishatu Muhammad,
  • Sani Sa'idu Bello,
  • Chinwe Euphemia Egwu,
  • Zainab Mohammed Chellube

DOI
https://doi.org/10.4081/idhm.2022.222
Journal volume & issue
Vol. 3, no. 1

Abstract

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Cadaba farinosa Forssk. (Capparaceae) is found all over the world, mostly in tropical and subtropical areas. It is used to treat pain, dysentery, rheumatism, cough, and fever, as well as an antidote and in the treatment of neurological disorders. In mice, the median lethal dose (LD50) of Crude Ethanol leaf Extract (CEE) of Cadaba farinosa was found to be 2154.1 mg/kg body weight. The presence of alkaloids, anthraquinones, carbohydrates, cardiac glycosides, flavonoids, glycosides, saponins, and tannins was discovered during a preliminary phytochemical analysis of the dark gummy mass crude extract. The CEE was then put through pharmacological testing on mice. In mice, diazepam-induced sleep, beam walking, and hole-board assays were used to investigate behavioral activities. CEE of Cadaba farinosa had no effect on the onset of sleep in mice when given at the tested doses of diazepam. In contrast, it significantly increased sleep duration at all doses tested (75 mg/kg p 0.001, 150 mg/kg p 0.05, and 300 mg/kg p 0.01). The CEE significantly (p 0.01) increased the number of foot slips in the Beam walking assay at a dose of 150 mg/kg. Similarly, diazepam at 0.25 mg/kg increased the number of foot slips significantly (p 0.001). The extract at a dose of 300 mg/kg and diazepam increased the time required to complete the task significantly (p 0.05). At 150 mg/kg (p 0.01) and 300 mg/kg (p 0.05), the hole-board experiment significantly reduced the number of head dips. In contrast, the standard drug (diazepam) had no discernible effect on the number of head dips. These findings suggest that Cadaba farinosa CEE has analgesic (both centrally and peripherally mediated) and anti-inflammatory properties.

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