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大麻成分与药物外排泵 BCRP 相互作用,显著增加血浆大麻素酸浓度。

Cannabis constituents interact at the drug efflux pump BCRP to markedly increase plasma cannabidiolic acid concentrations.

机构信息

Brain and Mind Centre, Discipline of Pharmacology, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.

Lambert Initiative for Cannabinoid Therapeutics, Brain and Mind Centre, The University of Sydney, 94 Mallett St, Camperdown, NSW, 2050, Australia.

出版信息

Sci Rep. 2021 Jul 22;11(1):14948. doi: 10.1038/s41598-021-94212-6.

Abstract

Cannabis is a complex mixture of hundreds of bioactive molecules. This provides the potential for pharmacological interactions between cannabis constituents, a phenomenon referred to as "the entourage effect" by the medicinal cannabis community. We hypothesize that pharmacokinetic interactions between cannabis constituents could substantially alter systemic cannabinoid concentrations. To address this hypothesis we compared pharmacokinetic parameters of cannabinoids administered orally in a cannabis extract to those administered as individual cannabinoids at equivalent doses in mice. Astonishingly, plasma cannabidiolic acid (CBDA) concentrations were 14-times higher following administration in the cannabis extract than when administered as a single molecule. In vitro transwell assays identified CBDA as a substrate of the drug efflux transporter breast cancer resistance protein (BCRP), and that cannabigerol and Δ-tetrahydrocannabinol inhibited the BCRP-mediated transport of CBDA. Such a cannabinoid-cannabinoid interaction at BCRP transporters located in the intestine would inhibit efflux of CBDA, thus resulting in increased plasma concentrations. Our results suggest that cannabis extracts provide a natural vehicle to substantially enhance plasma CBDA concentrations. Moreover, CBDA might have a more significant contribution to the pharmacological effects of orally administered cannabis extracts than previously thought.

摘要

大麻是一种由数百种生物活性分子组成的复杂混合物。这为大麻成分之间的药物相互作用提供了可能性,这种现象被药用大麻界称为“伴随效应”。我们假设大麻成分之间的药代动力学相互作用可能会极大地改变系统中的大麻素浓度。为了验证这一假设,我们比较了大麻提取物中口服给予大麻素与以等效剂量单独给予单个大麻素时的药代动力学参数。令人惊讶的是,大麻素酸(CBDA)在大麻提取物中的血浆浓度比单独给予时高 14 倍。体外 Transwell 测定鉴定出 CBDA 是药物外排转运蛋白乳腺癌耐药蛋白(BCRP)的底物,大麻二酚和 Δ-四氢大麻酚抑制了 CBDA 的 BCRP 介导的转运。位于肠道中的 BCRP 转运蛋白上的这种大麻素-大麻素相互作用会抑制 CBDA 的外排,从而导致血浆浓度增加。我们的结果表明,大麻提取物提供了一种天然载体,可以显著提高血浆 CBDA 浓度。此外,CBDA 可能对口服给予的大麻提取物的药理作用的贡献比以前认为的更大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be2/8298633/145b35482a0c/41598_2021_94212_Fig1_HTML.jpg

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