Planta Med 2009; 75(4): 295-301
DOI: 10.1055/s-0029-1185306
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Pharmacological Exploration of the Sedative Mechanism of Hesperidin Identified as the Active Principle of Citrus sinensis Flowers

Silvia Laura Guzmán-Gutiérrez1 [*] , Andrés Navarrete1
  • 1Facultad de Química, Departamento de Farmacia. Universidad Nacional Autónoma de México, México
Further Information

Publication History

received Sept. 1, 2008 revised Nov. 10, 1008

accepted Dec. 1, 2008

Publication Date:
13 February 2009 (online)

Abstract

The infusion of flowers of several species of Citrus genera is used as a sedative to treat insomnia in Mexican traditional medicine. The aims of this study were to investigate the sedative effect of different extracts of flowers of Citrus sinensis (L.) Osbeck (Rutaceae) and describe the pharmacological action mechanism of the sedative active compounds of this plant. The methanol and dichloromethane extracts, obtained from the flowers of Citrus sinensis (L.) Osbeck (Rutaceae), showed a dose-dependent sedative effect in the exploratory cylinder model in mice, with ED50 (i. p.) values of 47.04 ± 12.03 mg/kg and 129.15 ± 21.25 mg/kg, respectively. Hesperidin (ED50 = 11.34 ± 2.48 mg/kg) was identified in the methanol extract as the sedative active principle of this plant. The pre-treatment with atropine (1 mg/kg i. p.), flumazenil (2 mg/kg i. p.), clonidine (0.01 mg/kg i. p.), isoproterenol (0.3 mg/kg i. p.), haloperidol (0.3 mg/kg i. p.), WAY 100 635 (3 mg/kg i. p.), p-chlorophenylalanine (250 mg/kg i. p., twice per day for 2 days), forskolin (3 mg/kg i. p.) and rolipram (0.173 mg/kg i. p.) did not modify the sedative effect of 30 mg/kg hesperidin. However, the sedative effect of this compound was potentiated by yohimbine (1.25 mg/kg i. p.) and buspirone (1 mg/kg i. p.), and reverted by pretreatment with aminophylline (30 mg/kg i. p.), caffeine (30 mg/kg i. p.) and several doses of 1,3-dimethyl-8-phenylxanthine (10, 30 and 54.7 mg/kg i. p.). These results suggest that adenosine receptors might be involved in the sedative action of hesperidin, identified as the active principle of the flowers of Citrus sinensis.

References

  • 1 Nau S D, McCrae C S, Cook K G, Lichstein K L. Treatment of insomnia in older adults.  Clin Psychol Rev. 2005;  25 645-672
  • 2 Roth T. New developments for treating sleep disorders.  J Clin Psychiatry. 2001;  62 (Suppl. 10) 3-4
  • 3 Kamel N S, Gammack J K. Insomnia in the elderly: cause, approach, and treatment.  Am J Med. 2006;  119 463-469
  • 4 Benca R M. Diagnosis and treatment of chronic insomnia: a review.  Psychiatr Serv. 2005;  56 332-343
  • 5 Gottesmann C. GABA mechanisms and sleep.  Neuroscience. 2002;  111 231-239
  • 6 Wheatley D. Medicinal plants for insomnia: a review of their pharmacology, efficacy and tolerability.  J Psychopharmacol. 2005;  19 414-421
  • 7 Marder M, Viola H, Wasowski C, Fernández S, Medina J H, Paladini A C. 6-Methylapigenin and hesperidin: new valeriana flavonoids with activity on the CNS.  Pharmacol Biochem Behav. 2003;  75 537-545
  • 8 Garg A, Garg S, Zaneveld L JD, Sinlge A K. Chemistry and pharmacology of the citrus bioflavonoid hesperidin.  Phytother Res. 2001;  15 655-669
  • 9 Loscalzo L M, Wasowski C, Paladini A C, Marder M. Opioid receptors are involved in the sedative and antinociceptive effects of hesperidin as well as in its potentiation with benzodiazepines.  Eur J Pharmacol. 2008;  580 306-313
  • 10 Tortoriello J, Romero O. Plants used by Mexican traditional medicine with presumable sedative properties: an ethnobotanical approach.  Arch Med Res. 1992;  23 111-116
  • 11 Carvalho-Freitas M IR, Costa M. Anxiolytic and sedative effects of extracts and essential oil from Citrus aurantium L.  Biol Pharm Bull. 2002;  25 1629-1633
  • 12 Pultrini Ade M, Galindo L A, Costa M. Effects of the essential oil from Citrus aurantium L. in experimental anxiety models in mice.  Life Sci. 2006;  78 1720-1725
  • 13 Oliva I, González-Trujano M E, Arrieta J, Enciso-Rodriguez R, Navarrete A. Neuropharmacological profile of hydroalcoholic extract of Valeriana edulis ssp. procera roots in mice.  Phytother Res. 2004;  18 290-296
  • 14 Ugalde M, Reza V, González-Trujano M E, Avula B, Khan I A, Navarrete A. Isobolographic analysis of the sedative interaction between six central nervous system depressant drugs and Valeriana edulis hydroalcoholic extract in mice.  J Pharm Pharmacol. 2005;  57 631-639
  • 15 Li C, Gu H, Dou H, Zhou L. Identification of flavanones from peel of Citrus changshan-huyou Y.B. Chang, by HPLC‐MS and NMR.  Eur Food Res Technol. 2007;  225 777-782
  • 16 Hiller K, Zetler G. Neuropharmacological studies on ethanol extracts of Valeriana officinalis L.: behavioral and anticonvulsant properties.  Phytother Res. 1996;  10 145-151
  • 17 Tallarida R. Drug synergism and dose-effect data analisis. Boca Raton; Chapman and Hall/CRC Press 2000: 21-35
  • 18 Haapalinna A, Viitamaa T, MacDonald E, Savola J M, Tuomisto L, Virtanen R. Evaluation of the effects of a specific α2-adrenoceptor antagonist, atipamezole, on α1 and α2-adrenoceptor subtype binding, brain neurochemistry and behaviour in comparison with yohimbine.  Naunyn-Schmiedeberg's Arch Pharmacol. 1997;  356 570-582
  • 19 Warnick J E, Wicks R T, Sufka K J. Modeling anxiety-like states: pharmacological characterization of chick separation stress paradigm.  Behav Pharmacol. 2006;  17 581-587
  • 20 Winter J C, Rabin R A. Yohimbine as a serotonergic agent: evidence from receptor binding and drug discrimination.  J Pharmacol Exp Ther. 1992;  263 682-689
  • 21 Datta S, MacLean R R. Neurobiological mechanisms for the regulation of mammalian sleep-wake behavior: reinterpretation of historical evidence and inclusion of contemporary cellular and molecular evidence.  Neurosci Biobehav Rev. 2007;  31 775-824
  • 22 Kuno N, Kamisaki Y, Itoh T. Inhibition of cyclic AMP accumulation by α2-adrenoceptors in the rat cerebral cortex.  Eur J Pharmacol. 1990;  176 281-287
  • 23 Pauwels P J, Van Gompel P, Leysen J E. Activity of serotonin (5-HT) receptor agonists, partial agonists and antagonists at cloned human 5-HT1A receptors that are negatively coupled to adenylate cyclase in permanently transfected HeLa cells.  Biochem Pharmacol. 1993;  45 375-383
  • 24 Barnes P J. Pharmacology of airway smooth muscle.  Am J Respir Crit Care Med. 1998;  158 S123-132
  • 25 Ogasahara S, Taguchi Y, Wada H. Changes in the levels of cyclic nucleotides in rat brain during the sleep-wakefulness cycle.  Brain Res. 1981;  213 163-171
  • 26 Zhang H T, O'Donnell J M. Effects of rolipram on scopolamine-induced impairment of working and reference memory in the radial-arm maze tests in rats.  Psychopharmacology. 2000;  150 311-316
  • 27 Nehlig A, Daval J L, Debry G. Caffeine and the central nervous system: mechanism of action, biochemical, metabolic and psychostimulant effects.  Brain Res Rev. 1992;  17 139-170
  • 28 Fredholm B B, Persson C GA. Xantine derivatives as adenosine receptor antagonist.  Eur J Pharmacol. 1982;  81 673-676
  • 29 Satoh S, Matsumura H, Hayaishi O. Involvement of adenosine A2A receptor in sleep promotion.  Eur J Pharmacol. 1998;  351 155-162
  • 30 Ingkaninan K, Ijzerman A P, Verpoorte R. Leuteolin, a compound with adenosine A1 receptor-binding activity, and chromone and dihydronaphthalenone constituents from Senna siamea.  J Nat Prod. 2000;  63 315-317
  • 31 Blardi P, De Lalla A, Volpi L, Di Perri T. Stimulation of endogenous adenosine release by oral administration of quercetin and resveratrol in man.  Drugs Exp Clin Res. 1999;  25 105-110

1 Taken in part from the Ph.D. research work of S. L. Guzmán-Gutiérrez.

Dr. Andrés Navarrete

Facultad de Química, Departamento de Farmacia.
Universidad Nacional Autónoma de México

Ciudad Universitaria

Coyoacán 04510

México D. F.

México

Phone: + 55 56 22 52 91

Fax: + 55 56 22 53 29

Email: anavarrt@servidor.unam.mx

    >