Planta Med 2008; 74(10): 1229-1234
DOI: 10.1055/s-2008-1081288
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Chrysin Induces Hyperalgesia via the GABAA Receptor in Mice

Kui Zhai1 , Li Hu1 , Juan Chen1 , Cai-yun Fu1 , Qiang Chen1
  • 1Institute of Biochemistry and Molecular Biology, School of Life Science, Lanzhou University, Lanzhou, P. R. China
Further Information

Publication History

Received: April 14, 2008 Revised: May 14, 2008

Accepted: May 16, 2008

Publication Date:
08 July 2008 (online)

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Abstract

Chrysin (5,7-dihydroxyflavone) is a natural flavone commonly found in many plants including Passiflora coerulea L. Researchers have performed extensive and detailed investigations on the behavioral and pharmacological effects of chrysin in vivo, but there was little information available on the effect of chrysin on nociception. Therefore, the present study was undertaken to investigate the effect of chrysin on the nociceptive threshold using the tail-immersion test. Intraperitoneal (i. p.) injection of chrysin (10, 25, 50, 75, 100 mg/kg) dose- and time-dependently induced a pronounced decrease of the tail withdrawal latencies (TWL), thus characterizing a hyperalgesic effect (ED50 = 65.59 mg/kg). The following results showed that GABAA receptors were involved in the hyperalgesic effects of chrysin. 1) The hyperalgesia induced by chrysin was significantly and dose-dependently blocked by pretreatment with flumazenil (0.75, 1 mg/kg, i. p.), a specific antagonist for benzodiazepine sites associated with GABAA receptors. 2) Bicuculline (2, 4 mg/kg, i. p.), a GABAA receptor antagonist, markedly antagonized the hyperalgesic effect of chrysin in a dose-dependent manner. 3) Picrotoxin (2 mg/kg, i. p.), a chloride channel blocker, could also notably antagonize the hyperalgesia of chrysin. Oral administration of chrysin (75 mg/kg) also produced a hyperalgesic effect in the tail-immersion test. In addition, diazepam (1 mg/kg, i. p.) showed a marked antinociceptive effect, which was completely blocked by flumazenil (1 mg/kg, i. p.). In conclusion, it can be summarized that both i. p. and oral administration of chrysin produced a significant hyperalgesic effect in the tail-immersion test and that the hyperalgesic effect of chrysin may be associated with GABAA receptors.

Abbreviations

BDZ:benzodiazepine

DMSO:dimethyl sulfoxide

GABA:γ-aminobutyric acid

i. p.:intraperitoneal

NS:normal saline

TWL:tail-withdrawal latency

References

Prof. Qiang Chen, Ph.D.

Institute of Biochemistry and Molecular Biology

School of Life Science

Lanzhou University

222 Tian Shui South Road

*Lanzhou 730000

People’s Republic of China

Phone: +86/931/891/5316

Fax: +86/931/891/2428

Email: chenq@lzu.edu.cn