Planta Med 2005; 71(5): 406-411
DOI: 10.1055/s-2005-864133
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Mechanisms of Relaxant Action of Luteolin in Isolated Guinea Pig Trachea

Wun-Chang Ko1 , Chwen-Ming Shih2 , I-Jung Leu1 , Tzu-Ting Chen1 , Jung-Pei Chang1
  • 1Graduate Institute of Pharmacology, College of Medicine, Taipei Medical University, Taipei, Taiwan, R.O.C.
  • 2Department of Biochemistry, College of Medicine, Taipei Medical University, Taipei, Taiwan, R.O.C.
Further Information

Publication History

Received: August 18, 2004

Accepted: November 15, 2004

Publication Date:
01 June 2005 (online)

Preview

Abstract

We have investigated the mechanisms of action of luteolin, a flavone found in Perilla frutescens, a Chinese herbal medicine for treating asthma. In fact, luteolin occurs mostly as a glycoside in many plant species. The tension changes of tracheal segments were isometrically recorded on a polygraph. Luteolin concentration-dependently relaxed histamine (30 μM)-, carbachol (0.2 μM)- and KCl (30 mM)-induced precontractions, and inhibited cumulative histamine- and carbachol-induced contractions in a non-competitive manner. Luteolin also concentration-dependently and non-competitively inhibited cumulative Ca2+-induced contractions in depolarized (K+, 60 mM) guinea-pig trachealis. The nifedipine (10 μM)-remaining tension of histamine (30 μM)-induced precontractions was further relaxed by luteolin, suggesting that no matter whether VDCCs were blocked or not, luteolin may have other mechanisms of relaxant action. The relaxant effect of luteolin was unaffected by the removal of epithelium or by the presence of propranolol (1 μM), 2′,5′-dideoxyadenosine (10 μM), methylene blue (25 μM), glibenclamide (10 μM), N ω-nitro-l-arginine (20 μM), or α-chymotrypsin (1 U/mL). However, luteolin (10 - 20 μM) produced parallel and leftward shifts of the concentration-response curve of forskolin or nitroprusside. Luteolin or IBMX at various concentrations (10 - 300 μM) concentration-dependently and significantly inhibited cAMP- and cGMP-PDE activities of the trachealis. The IC50 values of luteolin were estimated to be 32.4 and 34.6 μM, respectively. IBMX at various concentrations (10 - 300 μM) selectively inhibited neither cAMP-, nor cGMP-PDE activity. In contrast to IBMX, luteolin at 100 and 300 μM more potently (P < 0.05) inhibited cGMP-, than cAMP-PDE activity. The above results indicate that the mechanisms of relaxant action of luteolin may be due to its inhibitory effects on both PDE activities and its reduction on [Ca2+]i of the trachealis.

Abbreviations

IBMX:3-isobutyl-1-methylxanthine

VDCCs:voltage dependent calcium channels

cAMP:adenosine 3′,5′-cyclic monophosphate

cGMP:guanosine 3′,5′-cyclic monophosphate

PDE:phosphodiesterase

References

Prof. Dr. Wun-Chang Ko

Graduate Institute of Pharmacology

College of Medicine

Taipei Medical University

250 Wu-Hsing St.

Taipei 110

Taiwan

R.O.C.

Fax: +886-2-2377-7639

Email: wc_ko@tmu.edu.tw