Planta Med 2001; 67(7): 609-613
DOI: 10.1055/s-2001-17356
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Effects of Hydrastine Derivatives on Dopamine Biosynthesis in PC12 Cells

So Hee Kim1 , Jeong Soo Shin1 , Jae Joon Lee1 , Shou Yu Yin1 , Masaaki Kai2 , Myung Koo Lee1,*
  • 1 College of Pharmacy, Chungbuk National University, Kaeshin-Dong, Heungduk-Ku, Cheongju, Republic of Korea
  • 2 Faculty of Pharmaceutical Sciences, Nagasaki University, Bunkyo-Machi, Nagasaki, Japan
Further Information

Publication History

October 18, 2000

December 17, 2000

Publication Date:
24 September 2001 (online)

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Abstract

The effects of hydrastine derivatives on dopamine biosynthesis in PC12 cells were investigated. Treatments of PC12 cells with (1R,9S)-β-hydrastine hydrochloride [(+)-β-hydrastine HCl] and (1R,9S)-β-hydrastine [(-)-β-hydrastine] showed 50.6 % and 33.1 % inhibition of dopamine content at a concentration of 10 μM for 48 h. However, (1S,9R)-β-hydrastine [(+)-β-hydrastine] and hydrastinine hydrochloride did not reduce dopamine content. The IC50 values of (1R,9S)-β-hydrastine hydrochloride and (1R,9S)-β-hydrastine were 9.3 μM and 20.7 μM, respectively. Next, the intracellular mechanisms of (1R,9S)-β-hydrastine hydrochloride in PC12 cells were investigated. Dopamine content decreased at 6 h and reached a minimal level at 24 h after the exposure of PC12 cells to 20 μM (1R,9S)-β-hydrastine hydrochloride. Tyrosine hydroxylase (TH) activity was inhibited at 6 h following the treatment with (1R,9S)-β-hydrastine hydrochloride, and was maintained at a reduced level for up to 36 h in PC12 cells (17 - 27 % inhibition at 20 μM), whereas TH mRNA level was not found to alter for 24 h. However, the level of intracellular Ca++ concentration decreased by treatment with (1R,9S)-β-hydrastine hydrochloride at 20 μM by 18.4 % inhibition relative to the control level in PC12 cells. These results suggest that (1R,9S)-β-hydrastine hydrochloride contributes partially to the decrease in dopamine content by the inhibition of TH activity in PC12 cells.

References

Myung Koo Lee, Ph. D.

College of Pharmacy

Chungbuk National University

San 48, Kaeshin-Dong

Heungduk-Ku

Cheongju 361-763

Republic of Korea

Email: myklee@cbucc.chungbuk.ac.kr

Fax: +82 (043) 268-2732