ANALGESIC, ANTI-INFLAMMATORY AND ANTIPYRETIC ACTIVITIES OF THE AQUEOUS EXTRACT OF GERANIUM CAROLINIANUM L

Authors

  • Yuan Li Second Military Medical University
  • Ying Ye
  • Su-Juan Wang
  • Wei Xia
  • Khalid Rahman
  • Wei Yue
  • Hong Zhang

DOI:

https://doi.org/10.21010/ajtcam.v13i1.15

Keywords:

Plant drug, Pain, Inflammation, Pyrexia, Toxicity, Animal

Abstract

Background: Geranium carolinianum L. (Geraniaceae) is widely used for a variety of diseases including herpetic keratitis, eczema, rheumatalgia etc. However, there is lack of relevant scientific research. Materials and Methods: GCE (125, 250, 500mg/kg body weight) was evaluated for its pharmacological properties by using the acetic acid-induced writhing test, the hot plate test and the fresh egg white-induced paw edema in rats. The dimethylbenzene-induced mouse inflammation model and the lipopolysaccharide (LPS)-induced rat fever model were employed and the acute toxicity of GCE was also assessed. Results: The Geranium carolinianum aqueous extract (GCE) significantly inhibited the writhing responses in mice, increased reaction time of mice in the hot plate test, and suppressed the fresh egg white-induced paw edema in rats and the dimethylbenzene-induced ear edema in mice whilst attenuating LPS-induced fever in rats in a dose dependent manner. Furthermore, no deaths were observed when mice were orally administered GCE up to 14 g/kg body weight (approximately 553 times of clinical dose). Conclusions: GCE possesses analgesic, anti-inflammatory and antipyretic activities and is non-toxic at the doses used. The results of this study support the clinical use and effectiveness of Geranium carolinianum as an analgesic, anti-inflammatory and antipyretic agent in folk medicine.

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Published

2015-12-03

How to Cite

Li, Y., Ye, Y., Wang, S.-J., Xia, W., Rahman, K., Yue, W., & Zhang, H. (2015). ANALGESIC, ANTI-INFLAMMATORY AND ANTIPYRETIC ACTIVITIES OF THE AQUEOUS EXTRACT OF GERANIUM CAROLINIANUM L. African Journal of Traditional, Complementary and Alternative Medicines, 13(1), 105–113. https://doi.org/10.21010/ajtcam.v13i1.15

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Section

Short communications