Planta Med 2009; 75(13): 1393-1399
DOI: 10.1055/s-0029-1185743
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

β2-Adrenoceptor-Mediated Tracheal Relaxation Induced by Higenamine from Nandina domestica Thunberg

Muneo Tsukiyama1 , 2 [*] , Takuro Ueki1 , 3 [*] , Yoichi Yasuda2 , Hiroko Kikuchi2 , Tatsuhiro Akaishi1 , Hidenobu Okumura2 , Kazuho Abe1
  • 1Laboratory of Pharmacology, Faculty of Pharmacy and Research Institute of Pharmaceutical Sciences, Musashino University, Tokyo, Japan
  • 2NOEVIR Co., Ltd., Kobe, Japan
  • 3TOKIWA Pharmaceutical Co., Ltd., Osaka, Japan
Further Information

Publication History

received Nov. 27, 2008 revised April 6, 2009

accepted April 14, 2009

Publication Date:
25 May 2009 (online)

Abstract

The fruit of Nandina domestica Thunberg (ND, Berberidaceae) has been used to improve cough and breathing difficulties in Japan for many years, but very little is known about the constituent of ND responsible for this effect. We have recently reported that the crude extract from ND (NDE) inhibits histamine- and serotonin-induced contraction of isolated guinea pig trachea, and the inhibitory activity was not explained by nantenine, a well-known alkaloid isolated from ND. To explore other constituent(s) of NDE with tracheal smooth muscle relaxant activity, we fractionated NDE and assessed the pharmacological effects of the fractions using isolated guinea pig tracheal ring preparations. NDE was introduced into a polyaromatic absorbent resin column and stepwise eluted to yield five fractions, among which only the 40 % methanol fraction was active in relaxing tracheal smooth muscle precontracted with histamine. Further separation of the 40 % methanol fraction with high-performance liquid chromatography yielded multiple subfractions, one of which was remarkably active in relaxing histamine-precontracted trachea. Chemical analysis with a time-of-flight mass spectrometer and nuclear magnetic resonance spectrometer identified the constituent of the most active subfraction as higenamine, a benzyltetrahydroisoquinoline alkaloid. The potency and efficacy of the active constituent from NDE in relaxing trachea were almost equivalent to synthetic higenamine. In addition, the effect of the active constituent from NDE was competitively inhibited by the selective β2-adrenoceptor antagonist ICI 118,551. These results indicate that the major constituent responsible for the effect of NDE is higenamine, which probably causes the tracheal relaxation through stimulation of β2 adrenoceptors.

References

  • 1 Takase T, Ohashi H. Chemische u. pharmakologische Studien über ein in den Früchten der Nandina domestica enthaltenes neues Alkaloid, Nantenin.  Yakugaku Zashhi. 1926;  535 742-748
  • 2 Shoji N, Umeyama A, Takemoto T, Ohizumi Y. Serotonergic receptor antagonist from Nandina domestica Thunberg.  J Pharm Sci. 1984;  73 568-570
  • 3 Indra B, Matsunaga K, Hoshino O, Suzuki M, Ogasawara H, Ohizumi Y. (±)-Domesticine, a novel and selective α1D-adrenoceptor antagonist in animal tissues and human α1-adrenoceptors.  Eur J Pharmacol. 2002;  445 21-29
  • 4 de Ribeiro R A, do Carmo L G, Vladimirova I, Jurkiewicz N H, Jurkiewicz A. Nantenine blocks muscle contraction and Ca2+ transient induced by noradrenaline and K+ in rat vas deferens.  Eur J Pharmacol. 2003;  470 37-43
  • 5 Tsukiyama M, Akaishi T, Ueki T, Okumura H, Abe K. The extract from Nandina domestica Thunberg inhibits histamine- and serotonin-induced contraction in isolated guinea pig trachea.  Biol Pharm Bull. 2007;  30 2063-2068
  • 6 Baumgartner R A, Wills-Karp M, Kaufman M J, Munakata M, Hirshman C. Serotonin induces constriction and relaxation of the guinea pig airway.  J Pharmacol Exp Ther. 1990;  255 165-173
  • 7 Christophe B, Carlier B, Gillard M, Chatelain P, Peck M, Massingham R. Histamine H1 receptor antagonism by cetirizine in isolated guinea pig tissues: influence of receptor reserve and dissociation kinetics.  Eur J Pharmacol. 2003;  470 87-94
  • 8 Abe K, Matsuki N, Kasuya Y. Pharmacological and electrophysiological discrimination of contractile responses to selective α1- and α2-adrenoceptor agonists in rat tail artery.  Jpn J Pharmacol. 1987;  45 249-261
  • 9 Waga T, Matsumoto K. Japanese Laid-Open Patent. 11–310531. 1999
  • 10 Park C W, Chang K C, Lim J K. Effects of higenamine on isolated heart adrenoceptor of rabbit.  Arch Int Pharmacodyn Ther. 1984;  267 279-288
  • 11 Chang K C, Lim J K, Park C W. Synthesis of higenamine and its cardiovascular effects in rabbit: evidence for β-adrenoceptor agonist.  Korean J Pharmacol. 1986;  22 96-104
  • 12 Kimura I, Chui L H, Fujitani K, Kikuchi T, Kimura M. Inotropic effects of (±)-higenamine and its chemically related components, (+)-R-coclaurine and (+)-S-reticuline, contained in the traditional Sino-Japanese medicines “Bushi” and “Shin-i” in isolated guinea pig papillary muscle.  Jpn J Pharmacol. 1989;  50 75-78
  • 13 Kimura I, Makino M, Takamura Y, Islam M A, Kimura M. Positive chronotropic and inotropic effects of higenamine and its enhancing action on the aconitine-induced tachyarrhythmia in isolated murine atria.  Jpn J Pharmacol. 1994;  66 75-80
  • 14 Carswell H, Nahorski S R. β-Adrenoceptor heterogeneity in guinea-pig airways: comparison of functional and receptor labelling studies.  Br J Pharmacol. 1983;  9 965-991
  • 15 Tanaka Y, Yamashita Y, Horinouchi T, Yamaki F, Koike K. Evidence showing that beta-adrenoceptor subtype responsible for the relaxation induced by isoprenaline is principally β2 but not β1 in guinea-pig tracheal smooth muscle.  Auton Autacoid Pharmacol. 2004;  24 37-43
  • 16 Bilski A J, Halliday S E, Fitzgerald J D, Wale J L. The pharmacology of a β2-selective adrenoceptor antagonist (ICI 118,551).  J Cardiovasc Pharmacol. 1983;  5 430-443
  • 17 Rimele T J, Henry D E, Giesa F R, Buckley S K, Geiger G, Heaslip R J, Lee D K, Grimes D. Comparison of the β-adrenoceptor affinity and selectivity of cetamolol, atenolol, betaxolol, and ICI‐118,551.  J Cardiovasc Pharmacol. 1988;  12 208-217
  • 18 Kang Y J, Lee Y S, Lee G W, Lee D H, Ryu J C, Yun-Choi H S, Yun-Choi H S, Chang K C. Inhibition of activation of nuclear factor κB is responsible for inhibition of inducible nitric oxide synthase expression by higenamine, an active component of Aconite root.  J Pharmacol Exp Ther. 1999;  291 314-320
  • 19 Yun-Choi H S, Pyo M K, Park K M, Chang K C, Lee D H. Anti-thrombotic effects of higenamine.  Planta Med. 2001;  67 619-622
  • 20 Bai G, Yang Y, Shi Q, Liu Z, Zhang Q, Zhu Y Y. Identification of higenamine in Radix Aconiti Lateralis Preparata as a beta2-adrenergic receptor agonist.  Acta Pharmacol Sin. 2008;  29 1187-1194
  • 21 Hao Z, Zhang Y, Pan L, Su X, Cheng M, Wang M, Zhao H, Wu Y. Comparison of enantiomers of SPFF, a novel β2-adrenoceptor agonist, in bronchodilating effect in guinea pigs.  Biol Pharm Bull. 2008;  31 866-872
  • 22 Yabana H, Watanabe H, Narita H, Nagao T. Selective and full β1-adrenoceptor agonist action of a catechol derivative of denopamine (T-0509) in the guinea-pig cardiac muscle and trachea: comparison with denopamine, xamoterol and isoprenaline.  Br J Pharmacol. 1992;  106 335-341
  • 23 Kosuge T, Yokota M. Studies on cardiac principle of aconite root.  Chem Pharm Bull. 1976;  24 176-178
  • 24 Kosuge T, Yokota M, Nagasawa M. Studies on cardiac principle of Aconite roots. Isolation and structure determination of higenamine.  Yakugaku Zasshi. 1978;  98 1370-1375
  • 25 Kosuge T, Yokota M, Nukaya H, Gotoh Y, Nagasawa M. Studies on antitussive principles of Asiasari radix.  Chem Pharm Bull. 1978;  26 2284-2285
  • 26 Xu Q, Lin M. Benzylisoquinoline alkaloids from Gnetum parvifolium.  J Nat Prod. 1999;  62 1025-1027

1 These authors contributed equally to this work.

Prof. Dr. Kazuho Abe

Laboratory of Pharmacology, Faculty of Pharmacy and Research Institute of Pharmaceutical Sciences
Musashino University

1–1–20 Shinmachi

Nishitokyo-shi

Tokyo 220–8585

Japan

Phone: + 81 4 24 68 91 65

Fax: + 81 4 24 68 91 65

Email: kazuabe@musashino-u.ac.jp

    >