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DOI: 10.1055/s-2008-1081288
© Georg Thieme Verlag KG Stuttgart · New York
Chrysin Induces Hyperalgesia via the GABAA Receptor in Mice
Publication History
Received: April 14, 2008
Revised: May 14, 2008
Accepted: May 16, 2008
Publication Date:
08 July 2008 (online)
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
Key words
Passiflora coerulea L. - Passifloraceae - chrysin - GABAA receptor - hyperalgesia - mice
References
- 1 Woodman O L, Chan E Ch. Vascular and anti-oxidant actions of flavonols and flavones. Clin Exp Pharmacol Physiol. 2004; 31 786-90
- 2 Elliott M, Chithan K, Theoharis C T. The effects of plant flavonoids on mammalian cells: implications for inflammation, heart disease, and cancer. Pharmacol Rev. 2000; 52 673-751
- 3 Medina J H, Paladini A C, Wolfman C, Levi de Stein M, Calvo D, Diaz L E. et al . Chrysin (5, 7-di-OH-flavone), a naturally-occurring ligand for benzodiazepine receptors, with anticonvulsant properties. Biochem Pharmacol. 1990; 40 2227-31
- 4 Wolfman C, Viola H, Paladini A, Dajas F, Medina J H. Possible anxiolytic effects of chrysin, a central benzodiazepine receptor ligand isolated from Passiflora coerulea. Pharmacol Biochem Behav. 1994; 47 1-4
- 5 Zanoli P, Avallone R, Baraldi M. Behavioral characterization of the flavonoids apigenin and chrysin. Fitoterapia. 2000; 71 117-23
- 6 Möhler H, Battersby M K, Richards J G. Benzodiazepine receptor protein identified and visualized in brain tissue by a photoaffinity label. Proc Natl Acad Sci USA. 1980; 77 1666-70
- 7 Gavish M, Snyder S H. γ-Aminobutytic acid and benzodiazepine receptors: copurification and characterization. Proc Natl Acad Sci USA. 1981; 78 1939-42
- 8 Salgueiro J B, Ardenghi P, Dias M, Ferreira M BC, Izquierdo I, Medina J H. Anxiolytic natural and synthetic flavonoid ligands of the central benzodiazepine receptor have no effect on memory tasks in rats. Pharmacol Biochem Behav. 1997; 58 887-91
- 9 Goutman J D, Waxemberg M D, Donate-Oliver F, Pomata P E, Calvo D J. Flavonoid modulation of ionic currents mediated by GABAA and GABAC receptors. Eur J Pharmacol. 2003; 461 79-87
- 10 Barnard E A, Skolnick P, Olsen R W, Mohler H, Sieghart W, Biggio G. et al . International union of pharmacology. XV. Subtypes of gamma-aminobutyric acidA receptors: classification on the basis of subunit structure and receptor function. Pharmacol Rev. 1998; 50 291-313
- 11 Hevers W, Ludens H. The diversity of GABAA receptors. Pharmacological and electrophysiological properties of GABAA channel subtypes. Mol Neurobiol. 1998; 18 35-86
- 12 Jasmin L, Rabkin S D, Granato A, Boudah A, Ohara P T. Analgesia and hyperalgesia from GABA-mediated modulation of the cerebral cortex. Nature. 2003; 424 316-20
- 13 Baumeister A A, Hawkins M F, Anderson-Moore L L, Anticich T G, Higgins T D, Griffin P. Effects of bilateral injection of GABA into the substantia nigra on spontaneous behavior and measures of analgesia. Neuropharmacology. 1988; 27 817-21
- 14 Drower E J, Hammond D L. GABAergic modulation of nociceptive threshold: effects of THIP and bicuculline microinjected in the ventral medulla of the rat. Brain Res. 1988; 45 316-24
- 15 Fu C Y, Kong Z Q, Wang K R, Yang Q, Zhai K, Chen Q. et al . Effects and mechanisms of supraspinal administration of rat/mouse hemokinin-1, a mammalian tachykinin peptide, on nociception in mice. Brain Res. 2005; 1056 51-8
- 16 Möhler H, Richards J G, Wu J Y. Autoradiographic localization of benzodiazepine receptors in immunocytochemically identified γ-aminobutyrergic synapses. Proc Natl Acad Sci USA. 1981; 78 1935-8
- 17 Richards J G, Schoch P, Häring P, Takacs B, Möhler H. Resolving GABAA /benzodiazepine receptors: cellular and subcellular localization in the CNS with momoclonal antibodies. J Neurosci. 1987; 7 1866-86
- 18 Macdonald R L, Olsen R W. GAbAa receptor channels. Annu Rev Neurosci. 1994; 17 569-602
- 19 Sieghart W. Structure and pharmacology of gamma-aminobutyric acid A receptor subtypes. Pharmacol Rev. 1995; 47 182-234
- 20 Tatsuo M AFK, Salgado J V, Yokoro C M, Duarte I DG, Francischi J N. Midazolam-induced hyperalgesia in rats: modulation via GABAA receptors at supraspinal level. Eur J Pharm. 1999; 370 9-15
- 21 Zambotti F, Zonta N, Tammiso R, Conci F, Hafner B, Zecca L. et al . Effects of diazepam on nociception in rats. Naunyn Schmiedebergs Arch Pharmacol. 1991; 344 84-9
- 22 Tejwani G A, Rattan A K, Sribanditmongkol P, Sheu M, Zuniga J, McDonald J S. Inhibition of morphine-induced tolerance and dependence by a benzodiazepine receptor agonist midazolam in the rat. Anesth Analg. 1993; 76 1052-60
- 23 Knabl J, Witschi R, Hösl K, Reinold H, Zeilhofer U B, Ahmadi S. et al . Reversal of pathological pain through specific spinal GABAA receptor subtypes. Nature. 2008; 451 330-4
- 24 Rosland J H, Hunskaar S, Hole K. The effect of diazepam on nociception in mice. Pharmacol Toxicol. 1987; 61 111-5
- 25 Wang H Y, Hui K M, Chen Y J, Xu S X, Wong T F, Xue H. Structure-activity relationships of flavonoids, isolated from Scutellaria baicalensis, binding to benzodiazepine site of GABAA receptor complex. Planta Med. 2002; 68 1059-62
- 26 Ewen A, Archer D P, Samanani N, Roth S H. Hyperalgesia during sedation: effects of barbiturates and propofol in the rat. Can J Anesth. 1995; 42 32-40
- 27 Oliveira D L, Horn J F, Rodrigues J M, Frizzo M ES, Moriguchi E, Souza D O. et al . Quinolinic acid promotes seizures and decreases glutamate uptake in young rats: reversal by orally administered guanosine. Brain Res. 2004; 1018 48-54
- 28 Kellis J T, Vickery L E. Inhibition of human estrogen synthetase (aromatase) by flavones. Science. 1984; 225 1032-4
- 29 Gambelunghe C, Rossi R, Sommavilla M, Ferranti C, Rossi R, Ciculi C. et al . Effects of chrysin on urinary testosterone levels in human males. J Med Food. 2003; 6 387-90
Prof. Qiang Chen, Ph.D.
Institute of Biochemistry and Molecular Biology
School of Life Science
Lanzhou University
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*Lanzhou 730000
People’s Republic of China
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