Brain Sciences (Sep 2020)

Mitigating Effects of <i>Liriope platyphylla</i> on Nicotine-Induced Behavioral Sensitization and Quality Control of Compounds

  • Dahye Yoon,
  • In Soo Ryu,
  • Woo Cheol Shin,
  • Minhan Ka,
  • Hyoung-Geun Kim,
  • Eun Young Jang,
  • Oc-Hee Kim,
  • Young-Seob Lee,
  • Joung-Wook Seo,
  • Dae Young Lee

DOI
https://doi.org/10.3390/brainsci10090654
Journal volume & issue
Vol. 10, no. 9
p. 654

Abstract

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In this study we investigated the mitigating effects of Liriope platyphylla Wang et Tang extract on behavioral sensitization and the quantification of its major compounds. The extract of L. platyphylla reduces the expression of tyrosine hydroxylase (TH) protein, which is increased by nicotine, back to normal levels, and increases the expression of dopamine transporter (DAT) protein, which is reduced by nicotine, back to normal levels in PC12 cells. In this study, rats received nicotine (0.4 mg/kg, subcutaneously) only for seven days and then received extract of L. platyphylla (200 or 400 mg/kg, oral) 1 h prior to nicotine administration for an additional seven days. The extract of L. platyphylla reduced locomotor activity compared to the nicotine control group in rats. The extract of L. platyphylla significantly attenuated the repeated nicotine-induced DAT protein expression in the nucleus accumbens (NAc), but there was no effect on increased TH protein expression in the dorsal striatum. These findings suggest that L. platyphylla extract has a mitigating effect on nicotine-induced behavioral sensitization by modulating DAT protein expression in the NAc. For quality control of L. plathyphylla, spicatoside A and D, which are saponin compounds, were quantified in the L. platyphylla extract. The amounts of spicatoside A and D in L. platyphylla extract obtained from ultra-high-performance liquid chromatography with tandem mass spectrometry were 0.148 and 0.272 mg/g, respectively. The identification of these compounds in L. platyphylla, which can be used for quality control, provides important information for the development of drugs to treat nicotine dependence.

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