Quantification of Meranzin Hydrate in Rat Hippocampus and Plasma by LC–MS/MS: A Compound Derived from Chaihu–Shugan–San Displays Antidepressant Potential

• Published in: Chromatographia 2015-02, Vol.78 (3-4), p.221-229
• Main Authors: Huang, Xi, He, Yijing, Huang, Weihua, Tan, Zhirong, Peng, Jingbo, Wang, Yicheng, Guo, Ying, Hu, Dongli, Ou-Yang, Dong-sheng, Wang, Yang, Luo, Min, Chen, Yao
• Format: Article
• Language: English
• Subjects: acetonitrile; Analytical Chemistry; antidepressants; Chemistry; Chemistry and Materials Science; Chromatography; hippocampus; intragastric administration; ionization; Laboratory Medicine; Original; Pharmacy; Proteomics; rats
• ISSN: 0009-5893; 1612-1112
• DOI: 10.1007/s10337-014-2838-y

Meranzin hydrate (MH), a compound derived from Chaihu–Shugan–San (CSS), displayed potent preclinical antidepressant functions. In this study, an LC–MS/MS method was developed and validated to quantify the MH in rat hippocampus and plasma. Tert-butyl methyl ether and irbesartan were used as the extraction reagent and the internal standard (IS), respectively. Chromatographic separation was achieved on a C₁₈column using the mobile phase, which consisted of a 20 mM solution of ammonium formate and acetonitrile at a ratio of 60:40. The flow rate was set at 0.3 mL min⁻¹. The detection was performed by multiple reactions monitored in a positive ion mode via electrospray ionization. The transitions were monitored by m/z 279.1 → 188.9 for MH and m/z 429.0 → 206.9 for IS. Linear calibration curves were obtained in the concentration range of 0.70–278.29 ng mL⁻¹, with a lower limit of quantification of 0.70 ng mL⁻¹. The intra- and inter-day precision values were below 11.9 % relative standard deviation, and the accuracy was from 90.5 to 107.5 %. The recovery was from 85.7 to 89.5 %. The LC–MS/MS method was applied to quantify the MH in hippocampus tissue compared with that in plasma after intragastric administration of MH (9 mg kg⁻¹) to rats. The results showed that the AUC₍₀–₄₈₀₎, AUC₍₀–ᵢₙfᵢₙᵢₜy₎, and Cₘₐₓvalues of MH in plasma were much higher than those values in the hippocampus of rats. Our study established a sensitive, reliable, and specific LC–MS/MS method for quantification of MH and confirmed the existence of MH in the rat hippocampus, which may contribute to antidepression mechanism research for MH in further study.