Planta Med 2003; 69(4): 332-336
DOI: 10.1055/s-2003-38878
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Stimulatory Effect of Paeoniflorin on Adenosine Release to Increase the Glucose Uptake into White Adipocytes of Wistar Rat

Lap-Ming Tang1 , I-Min Liu2, 3 , Juei-Tang Cheng3
  • 1Department of Emergency Medicine, Mackay Memorial Hospital, Taipei City, Taiwan, R.O.C.
  • 2Department of Pharmacy, Tajen Institute of Technology, Yen-Pou, Ping Tung Shien, Taiwan, R.O.C.
  • 3Department of Pharmacology, College of Medicine, National Cheng Kung University, Tainan City, Taiwan, R.O.C.
Weitere Informationen

Publikationsverlauf

Received: July 5, 2002

Accepted: December 7, 2002

Publikationsdatum:
23. April 2003 (online)

Abstract

The present study investigated the role of adenosine in the stimulatory action of paeoniflorin on in vitro glucose transport. Paeoniflorin increased the uptake of a radiolabeled, non-metabolizable glucose derivative into isolated white adipocytes of Wistar rat in a concentration-dependent manner and this action was abolished by the antagonist, 8-cyclopentyltheophylline, at concentrations sufficient to block the adenosine A1 receptor. However, paeoniflorin failed to displace the binding of [3 H]-8-cyclopentyl-1,3-dipropylxanthine in the isolated cerebrocortex of Wistar rat. Direct activation of the adenosine A1 receptor does not seem to be responsible for the action of paeoniflorin. The stimulatory effect of paeoniflorin on radioactive glucose uptake was abolished in isolated rat white adipocytes pre-incubated with the adenosine deaminase at concentrations sufficient to metabolize endogenous adenosine. Mediation of endogenous adenosine in the action of paeoniflorin was further supported by the assay of adenosine released into the medium from rat white adipocytes incubated with paeoniflorin. These findings suggest that paeoniflorin could induce the release of adenosine from isolated rat white adipocytes and the released adenosine may activate the adenosine A1 receptor to enhance glucose uptake.

References

  • 1 Hattori M, Shu Y Z, Shimizu M, Hayashi T, Morita N, Kobashi K, Xu G J, Namba T. Metabolism of paeoniflorin and related compounds by human intestinal bacteria.  Chem Pharm Bull. 1985;  33 3838-46
  • 2 Goto H, Shimada Y, Akechi Y. Endothelium-dependent vasodilator effect of extract prepared from the roots of Paeonia lactiflora on isolated rat aorta.  Planta Med. 1996;  62 436-9
  • 3 Satoh K, Nagai F, Ushiyama K, Yasuda I, Seto T, Kano I. Inhibition of Na+,K+-ATPase by 1,2,3,4,6-penta-O-galloyl-β-d-glucose, a major constituent of both Moutan cortex and Paeoniae radix.  Biochem Pharmacol. 1997;  53 611-4
  • 4 Yoshizaki M, Tomimori T, Yoshioka S, Namba T. Fundamental studies on the evaluation of the crude drugs. V. Quantitative analysis of constituents in crude drugs by rod-thin-layer chromatography with FID. (2). Determination of paeoniflorin and albiflorin in paeony roots (in Japanese).  Yakugaku Zasshi. 1977;  97 916-21
  • 5 Hsu F L, Lai C W, Cheng J T. Antihyperglycemic effects of paeoniflorin and 8-debenzoylpaeoniflorin, glucosides from the root of Paeonia lactiflora .  Planta Med. 1997;  63 323-5
  • 6 Watanabe H. Candidates for cognitive enhancer extracted from medicinal plants: paeoniflorin and tetramethylpyrazine.  Behav Brain Res. 1997;  83 135-41
  • 7 Abdel-Hafez A A, Meselhy M R, Nakamura N, Hattori M, Watanabe H, Mohamed T A, Mahfouz N M, El-Gendy M A. Potent anticonvulsant paeonimetabolin-I derivatives obtained by incubation of paeoniflorin and thiol compounds with Lactobacillus brevis .  Chem Pharm Bull. 1998;  46 1486-7
  • 8 Dezaki K, Kimura I, Miyahara K, Kimura M. Complementary effects of paeoniflorin and glycyrrhizin on intracellular Ca2+ mobilization in the nerve-stimulated skeletal muscle of mice.  Jpn J Pharmacol. 1995;  69 281-4
  • 9 Tamaya T, Sato S, Okada H H. Possible mechanism of steroid action of the plant herb extracts glycyrrhizin, glycyrrhetinic acid, and paeoniflorin: inhibition by plant herb extracts of steroid protein binding in the rabbit.  J Obs Gyn. 1986;  155 1134-9
  • 10 Ohta H, Matsumoto K, Watanabe H, Shimizu M. Involvement of β-adrenergic systems in the antagonizing effect of paeoniflorin on the scopolamine-induced deficit in radial maze performance in rats.  Jpn J Pharmacol. 1993;  62 345-9
  • 11 Lai C W, Hsu F L. Cheng JT. Stimulatory effect of paeoniflorin on adenosine A-1 receptors to increase the translocation of protein kinase C (PKC) and glucose transporter (GLUT 4) in isolated rat white adipocytes.  Life Sci. 1998;  62 591-5
  • 12 Smith U, Kuroda M, Simpson I A. Counter-regulation of insulin-stimulated glucose transport by catecholamines in the isolated rat adipose cell.  J Biol Chem. 1984;  259 8758-63
  • 13 Schwabe U, Schonhofer P S, Ebert R. Facilitation by adenosine of the action of insulin on the accumulation of adenosine 3′:5′-monophosphate, lipolysis, and glucose oxidation in isolated fat cells.  Eur J Biochem. 1974;  46 537-45
  • 14 Mersmann H J, Carey G B, Smith B O. Influence of nutritional weaning on porcine adipocyte beta-adrenergic and adenosine A1 receptors.  J Animal Sci. 1997;  75 2368-77
  • 15 Maemoto T, Finlayson K, Olverman H J, Akahane A, Horton R W, Butcher S P. Species differences in brain adenosine A1 receptor pharmacology revealed by use of xanthine and pyrazolopyridine based antagonists.  Br J Pharmacol. 1997;  122 1202-8
  • 16 Cheng J T, Liu I M, Chi T C, Shinozuka K, Lu F H, Wu T J, Chang C J. Role of adenosine in insulin-stimulated release of leptin from isolated white adipocytes of Wistar rats.  Diabetes. 2000;  49 20-4
  • 17 Pessin J E, Bell G I. Mammalian facilitative glucose transporter family: structure and molecular regulation.  Annu Rev Physiol. 1992;  54 911-30
  • 18 Saggerson E D, Jamal Z. Differences in the properties of A1-type adenosine receptors in rat white and brown adipocytes.  Biochem J. 1990;  269 157-61
  • 19 Liu I M, Lai T Y, Tsai C C, Cheng J T. Characterization of adenosine A1 receptor in cultured myoblast C2C12 cells of mice.  Auton Neurosci Basic & Clinic. 2001;  87 59-64
  • 20 Wong E H, Ooi S O, Loten E G, Sneyd J G. The action of adenosine in relation to that of insulin on the low-Km cyclic AMP phosphodiesterase in rat adipocytes.  Biochem J. 1985;  227 815-51
  • 21 Wong E H, Smith J A, Jarett L. Effect of adenosine on insulin activation of rat adipocyte pyruvate dehydrogenase.  FEBS Lett. 1984;  175 68-71
  • 22 Sakura N. Adenosine deaminase.  Jpn J Clin Med. 1995;  53 99-302
  • 23 Torres M, Molina P, Miras-Portugal M T. Adenosine transporters in chromaffin cells. Quantification by dipyridamol monoacetate.  FEBS Lett. 1986;  201 124-8

Prof. Juei-Tang Cheng

Department of Pharmacology, College of Medicine

National Cheng Kung University

Tainan City

Taiwan 70101

R.O.C.

Telefon: +886-6-237-2706

Fax: +886-6-238-6548

eMail: jtcheng@mail.ncku.edu.tw

    >