Inhibition of Tyrosine Hydroxylase by Palmatine

  • Published : 1996.08.01

Abstract

Palmatine, an protoberberine isoquinoline alkaloid, has been found to inhibit dopamine biosynthesis by reducing tyrosine hydroxylase (TH) activity in PC12 cells (Lee and Kim, 1996). We have therefore investigated the effects of palmatine on bovine adrenal TH. Palmatine showed a mild inhibition on bovine adrenal TH (36.4% inhibition at concentration of $200\muM$). Bovine adrenal TH was inhibited competitively by palmatine with a substrate L-tyrosine. The Ki value was found to be 0.67 mM. This result suggests that the inhibition of TH activity by palmatine may be partially involved in the reduction of dopamine biosynthesis in PC12 cells.

Keywords

References

  1. J. Med. Chem. v.33 Inhibition of monoamine oxidases A and B by simple isoquinoline alkaloids : Racemic and optically active 1,2,3,4-tetrahydro-, 3,4-dihydro-, and fully aromatic isoquinolines Bembeneck,M.E.;Abell,C.W.;Chrisey,L.A.
  2. Chin. J. Pharm. Anal. v.4 Dose dependent relationship of analgesic effect of Corydalis app.(Papaveraceae) in mice Chen,S.H.;Sha,N.H.
  3. Molekul. Biolog. v.28 Kinetic analysis of interaction of human immunodeficiency virus reverse transcriptase with alkaloids Gudima,S.O.;Memelova,L.V.;Borodulin,V.B.;Pokholok,D.K.;Mednikov,B.M.;Tolkachev,O.N.;Kochetkov,S.N.
  4. Japan J. Pharmacol. v.61 Effects of palmatine on motor activity and the concentration of central monoamines and its metabolites in rats Hsieh,M.T.;Su,S.H.;Tsai,H.Y.;Peng,W.T.;Hsieh,C.C.;Chen,C.F.
  5. Immunohistochemistry Oxford IBRO Handbook Preparation of catecholamine-synthesizing enzymes as immunogens for immunohistochemistry Joh,T.H.;Ross,M.E.;Cuello,A.C.(ed.)
  6. Cancer Lett. v.93 Berberine complexes with DNA in the berberine-induced apoptosis in human leukemic HL-60 cells Kuo,C.L.;Chou,C.C.;Yung,B.Y.M.
  7. Arch. Pharm. Res. v.17 Inhibitory effects of the root of Coptis japonica on catecholamine biosynthesis in PC12 cells Lee,M.K.;Park,W.K.;Kim,H.S.
  8. Planta Med. v.62 Inhibitory effects of the protoberberine alkaloids from the root of Coptis japonica on catecholamine biosynthesis in PC12 cells Lee,M.K.;Kim,H.S.
  9. J. Biol. Chem. v.193 Protein measurement with the Folin phenol reagent Lowry,O.H.;Rosebrough,N.J.;Farr,A.L.;Randall,R.J.
  10. Bull. Chin. Materia Med. v.10 Screening test of antiarrythmia effect of Corydalis turtschaninovii(Papaveraceae) in rats Ma,S.S.;Chen,K.G.;Ma,Y.L.;Bau,S.F.
  11. J. Neurochem. v.58 Inhibition of tyrosine hydroxylase by R and S enantimers salsolinol, 1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline Minami,M.;Takahashi,T.;Maruyama,A.;Takahashi,A.;Dostert,P.;Nagatsu,T.;Naoi,M.
  12. J. Biol. Chem. v.239 Tyrosine hydroxylase: The initial step in norepinephrine biosynthesis Nagatsu,T.;Levitt,M.;Udenfriend,S.
  13. J. Chromatogr. v.163 Highly sensitive assay for tyrosine hydroxylase activity by high-performance liquid chromatography Nagatau,T.;Oka,K.;Kato,K.
  14. J. Neurochem. v.50 Inhibition of type A monoamine oxidase by methylquinolines and structurally related compounds Naoi,M.;Nagatsu,T.
  15. Neurochem. Int. v.15 N-Methylisoquinolinim ion as an inhibitor of tyrosine hydroxylase, aromatic L-amino acid decarboxylase and monoamine oxidase Naoi,M.;Takahashi,T.;Darrez,H.;Kabeya,R.;Taguchi,E.
  16. Neurochem. Int. v.15 (±)Tetrahydroanisocycline and (±)tetrahydropalmatine binding to D₁and D ₂dopaminergic receptors in human putamen Vauquelin,G.;De Keyser,J.;Kanyinda,B.;Vanhaelen,M.
  17. J. Med. Chem. v.31 Protoberberine alkaloids as antimalarials Vennerstrom,J.L.;Klayman,D.L.