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大麻二酚(CBD)对大鼠脂质吸收和淋巴转运的影响。

The Impact of Cannabidiol (CBD) on Lipid Absorption and Lymphatic Transport in Rats.

作者信息

Zhu Qi, Yang Qing, Shen Ling, Xu Meifeng, Liu Min

机构信息

Department of Pathology and Laboratory Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA.

出版信息

Nutrients. 2025 Mar 15;17(6):1034. doi: 10.3390/nu17061034.

DOI:10.3390/nu17061034
PMID:40292467
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11944757/
Abstract

Cannabidiol (CBD) exerts diverse metabolic effects, yet its influence on intestinal lipid metabolism remains unclear. In this study, we investigated whether short-term (one-week) CBD treatment affects lipid absorption and transport through the lymphatic system using a validated lymph fistula model. CBD treatment significantly enhanced the transport of radiolabeled triglycerides through the lymphatic system. This effect appeared specific, as CBD did not substantially alter cholesterol output in the lymph. Chemical assays indicated that CBD treatment did not significantly alter total triglycerides, cholesterol, phospholipids, or non-esterified fatty acid levels in the lymph. However, it significantly enhanced the lymphatic output of apolipoprotein A4 (ApoA4) and apolipoprotein A1 (ApoA1). Additionally, gene expression analysis revealed a downregulation of vascular endothelial growth factor receptor 1 (Flt1) in the small intestine, leading to increased lymphatic lacteal permeability and altered lipid transport dynamics. These findings indicate that short-term CBD treatment modulates lymphatic lipid composition and apolipoprotein secretion by regulating lymphatic lacteal function, thereby influencing lipid transport and metabolism. This study provides novel insights into CBD's role in facilitating TG-rich lipoprotein transport via the lymphatic system, highlighting its potential therapeutic applications in lipid-related disorders.

摘要

大麻二酚(CBD)具有多种代谢作用,但其对肠道脂质代谢的影响尚不清楚。在本研究中,我们使用经过验证的淋巴瘘模型,研究了短期(一周)CBD治疗是否会影响脂质通过淋巴系统的吸收和运输。CBD治疗显著增强了放射性标记甘油三酯通过淋巴系统的运输。这种作用似乎具有特异性,因为CBD并未显著改变淋巴中胆固醇的输出。化学分析表明,CBD治疗并未显著改变淋巴中总甘油三酯、胆固醇、磷脂或非酯化脂肪酸的水平。然而,它显著增强了载脂蛋白A4(ApoA4)和载脂蛋白A1(ApoA1)的淋巴输出。此外,基因表达分析显示小肠中血管内皮生长因子受体1(Flt1)下调,导致淋巴乳糜管通透性增加和脂质运输动力学改变。这些发现表明,短期CBD治疗通过调节淋巴乳糜管功能来调节淋巴脂质组成和载脂蛋白分泌,从而影响脂质运输和代谢。本研究为CBD在促进富含甘油三酯的脂蛋白通过淋巴系统运输中的作用提供了新的见解,突出了其在脂质相关疾病中的潜在治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/550be7c4503f/nutrients-17-01034-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/49e7bcfbe893/nutrients-17-01034-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/8051ba838d0e/nutrients-17-01034-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/178b35811512/nutrients-17-01034-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/9b63706f4f39/nutrients-17-01034-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/550be7c4503f/nutrients-17-01034-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/49e7bcfbe893/nutrients-17-01034-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/8051ba838d0e/nutrients-17-01034-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/178b35811512/nutrients-17-01034-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/9b63706f4f39/nutrients-17-01034-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/11944757/550be7c4503f/nutrients-17-01034-g005.jpg

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Nutrients. 2025 Mar 15;17(6):1034. doi: 10.3390/nu17061034.
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本文引用的文献

1
The Modulatory Effects and Therapeutic Potential of Cannabidiol in the Gut.大麻二酚在肠道中的调节作用和治疗潜力。
Cells. 2024 Sep 26;13(19):1618. doi: 10.3390/cells13191618.
2
Apolipoprotein A1 and high-density lipoprotein limit low-density lipoprotein transcytosis by binding SR-B1.载脂蛋白A1和高密度脂蛋白通过结合SR-B1限制低密度脂蛋白的转胞吞作用。
J Lipid Res. 2024 Apr;65(4):100530. doi: 10.1016/j.jlr.2024.100530. Epub 2024 Mar 12.
3
The Effect of Orally Administered Δ9-Tetrahydrocannabinol (THC) and Cannabidiol (CBD) on Obesity Parameters in Mice.
口服 Δ9-四氢大麻酚(THC)和大麻二酚(CBD)对小鼠肥胖参数的影响。
Int J Mol Sci. 2023 Sep 7;24(18):13797. doi: 10.3390/ijms241813797.
4
Chylomicrons Regulate Lacteal Permeability and Intestinal Lipid Absorption.乳糜微粒调节乳糜管通透性和肠道脂质吸收。
Circ Res. 2023 Aug 4;133(4):333-349. doi: 10.1161/CIRCRESAHA.123.322607. Epub 2023 Jul 18.
5
Inhibition of Vascular Inflammation by Apolipoprotein A-IV.载脂蛋白A-IV对血管炎症的抑制作用。
Front Cardiovasc Med. 2022 Jun 30;9:901408. doi: 10.3389/fcvm.2022.901408. eCollection 2022.
6
Effects of Cannabidiol on Locomotor Activity.大麻二酚对运动活性的影响。
Life (Basel). 2022 Apr 27;12(5):652. doi: 10.3390/life12050652.
7
Sexual dimorphism in intestinal absorption and lymphatic transport of dietary lipids.膳食脂质在肠道吸收和淋巴转运中的性别二态性。
J Physiol. 2021 Nov;599(22):5015-5030. doi: 10.1113/JP281621. Epub 2021 Oct 31.
8
Inclusion of Medium-Chain Triglyceride in Lipid-Based Formulation of Cannabidiol Facilitates Micellar Solubilization In Vitro, but In Vivo Performance Remains Superior with Pure Sesame Oil Vehicle.在大麻二酚的脂质制剂中加入中链甘油三酯有助于体外胶束增溶,但纯芝麻油载体的体内性能仍然更优。
Pharmaceutics. 2021 Aug 27;13(9):1349. doi: 10.3390/pharmaceutics13091349.
9
The Endocannabinoid System: A Potential Target for the Treatment of Various Diseases.内源性大麻素系统:治疗各种疾病的潜在靶点。
Int J Mol Sci. 2021 Aug 31;22(17):9472. doi: 10.3390/ijms22179472.
10
Natural sesame oil is superior to pre-digested lipid formulations and purified triglycerides in promoting the intestinal lymphatic transport and systemic bioavailability of cannabidiol.天然芝麻油优于预消化脂肪乳剂和纯化甘油三酯,可促进大麻二酚的肠淋巴转运和全身生物利用度。
Eur J Pharm Biopharm. 2021 May;162:43-49. doi: 10.1016/j.ejpb.2021.02.013. Epub 2021 Mar 5.