Planta Med 2003; 69(4): 310-315
DOI: 10.1055/s-2003-38874
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

3-O-Methylquercetin More Selectively Inhibits Phosphodiesterase Subtype 3

Wun-Chang Ko1 , Mei-Chun Chen1 , Sheng-Hao Wang1 , Ya-Hsin Lai1 , Jun-Hao Chen1 , Chun-Nan Lin2
  • 1Graduate Institute of Pharmacology, School of Medicine, Taipei Medical University, Taipei, R.O.C.
  • 2School of Pharmacy, Kaoshiung Medical University, Kaoshiung, Taiwan, R.O.C.
Further Information

Publication History

Received: August 5, 2002

Accepted: November 23, 2002

Publication Date:
23 April 2003 (online)

Abstract

Rhamnus nakaharai Hayata (Rhamnaceae), has been used as a folk medicine in Taiwan for treating constipation, inflammation, tumors and asthma. 3-O-Methylquercetin (3-MQ), a main constituent of the plant, has been reported to inhibit total cAMP- and cGMP-phosphodiesterase (PDE) of guinea pig trachealis. Therefore we were interested in investigating the inhibitory effect of 3-MQ on various PDE isozymes from guinea pig lungs and hearts. Isolated guinea pig lungs and hearts were homogenized and centrifuged. The supernatant was chromatographed over a column of Q-sepharose, and eluted with various concentrations of NaCl. In the following order, PDE subtypes 1, 5, 2, 4 from lungs, and 3 from hearts were separated. The IC50 values of 3-MQ on these isozymes were 31.9, 86.9, 18.6, 28.5 and 1.6 μM, respectively. 3-MQ (10 - 100 μM) non-competitively inhibited PDE2, but competitively inhibited PDE4. 3-MQ (1 - 10 μM) also competitively inhibited PDE3. However, 3-MQ (10 - 100 μM) did not competitively inhibit PDE1 and 5, although it had a tendency to competitively inhibit PDE1 at concentrations of 10 - 30 μM. The present results showed that Ki value of 3-MQ was similar to that of milrinone in PDE3, and was not significantly different from that of Ro 20 - 1724 in PDE4, respectively. In conclusion, 3-MQ was revealed to be a selective and competitive PDE3/PDE4 inhibitor, although its inhibitory effect on PDE4 was not potent. Therefore, 3-MQ may have a potential in the treatment of asthma beside its antiviral activity.

Abbreviations

3-MQ:3-O-methylquercetin

PDE:phosphodiesterase

cAMP:adenosine 3′,5′ cyclic monophosphate

cGMP:guanosine 3′,5′ cyclic monophosphate

EGTA:ethylene glycol-bis(β-aminoethyl ether), N,N,N′,N′-tetraacetic acid

EDTA:ethylenediaminetetraacetic acid

BSA:bovine serum albumin

PMSF:phenylmethanesulfonyl fluoride

EHNA:erythro-9-(2-hydroxy-3-nonyl)-adenine HCl

Ro 20-1724:4-(3-butoxy-4-methoxybenzyl)-2-imidazolidinone

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Prof. Dr. Wun-Chang Ko

Graduate Institute of Pharmacology

School of Medicine

Taipei Medical University

250 Wu-Hsing St.

Taipei 110

Taiwan, R.O.C.

Email: wc_ko@tmu.edu.tw

Fax: +886-2-2377-7639