Ma Hai-Qiu, Ebrahimi Forough, Low Bin-Seng, Khan Nurzalina Abdul Karim, Chan Kit-Lam
School of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800, Minden, Penang, Malaysia.
School of Medicine, Taylor's University, 47500, Subang Jaya, Selangor, Malaysia.
Phytother Res. 2017 Dec;31(12):1875-1882. doi: 10.1002/ptr.5930. Epub 2017 Sep 26.
Eurycoma longifolia Jack is popularly sought in Southeast Asian countries for traditional remedies to improve sexual performance and fertility. 13α(21)-Epoxyeurycomanone and eurycomanone, two major quassinoids in a root extract (TAF2) were reported to improve rat spermatogenesis and fertility. Unfortunately, these quassinoids possess low bioavailability because of high aqueous solubility and low lipid membrane permeability. Often, other possible barriers may be P-glycoprotein (P-gp) efflux in the gut and presystemic hepatic metabolism. The present study attempted to solve these problems by formulating a lipid-based solid dispersion (TAF2-SD) of optimized mixture of TAF2 and emulsifiers, which was then orally administered to rats prior to sperm count analysis. The TAF2-SD-treated rats showed significantly twofold (p < 0.001) and fourfold (p < 0.001) higher sperm count than did TAF2-treated and vehicle-treated (control) rats, respectively. The study also demonstrated no significant in vitro ileal absorption changes of the quassinoids by P-gp efflux inhibitors and concentration change or secondary metabolite formation upon in vitro incubation with rat liver homogenates, suggesting that P-gp-mediated efflux and presystemic metabolism were not limiting their bioavailability. Further study on orally TAF2-treated rats confirmed that the area under the curve and bioavailability curve of each quassinoid in the absence and presence of ketoconazole were unchanged. Copyright © 2017 John Wiley & Sons, Ltd.
长叶刺蒺藜在东南亚国家广受欢迎,被用于传统疗法以提高性功能和生育能力。据报道,根部提取物(TAF2)中的两种主要苦味素13α(21)-环氧刺蒺藜酮和刺蒺藜酮可改善大鼠精子发生和生育能力。不幸的是,由于这些苦味素具有高水溶性和低脂质膜通透性,其生物利用度较低。通常,其他可能的障碍可能是肠道中的P-糖蛋白(P-gp)外排和肝前体代谢。本研究试图通过制备TAF2与乳化剂的优化混合物的脂质基固体分散体(TAF2-SD)来解决这些问题,然后在精子计数分析前将其口服给予大鼠。与TAF2处理组和赋形剂处理组(对照组)大鼠相比,TAF2-SD处理组大鼠的精子计数分别显著高出两倍(p < 0.001)和四倍(p < 0.001)。该研究还表明,P-gp外排抑制剂对苦味素的体外回肠吸收没有显著变化,并且与大鼠肝匀浆体外孵育后浓度没有变化或没有形成次级代谢产物,这表明P-gp介导的外排和肝前体代谢并没有限制它们的生物利用度。对口服TAF2处理大鼠的进一步研究证实,在不存在和存在酮康唑的情况下,每种苦味素的曲线下面积和生物利用度曲线均未改变。版权所有© 2017 John Wiley & Sons, Ltd.