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基于微乳液的药物递送系统将胡椒生物碱鉴定为抗肥胖化合物。

Microemulsion-based drug delivery system identifies pepper alkaloids as anti-obesity compounds.

作者信息

Meng Tian-Kai, Han Ruo-Lei, Ma Peng, Chen Shu-Xin, Qi Bo-Han, Wang Zi-Xuan, Li Xiao-Yu, Deng Han-Song

机构信息

Yangzhi Rehabilitation Hospital, Sunshine Rehabilitation Center, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.

出版信息

Acta Pharmacol Sin. 2025 Mar 20. doi: 10.1038/s41401-025-01521-x.

Abstract

Obesity is a significant contributor to various metabolic diseases such as heart disease and diabetes. Due to the adverse effects of synthetic anti-obesity drugs, natural products from functional food plants, which mimic the effects of synthetic chemicals, present promising alternatives. However, many natural plant-derived compounds are poorly soluble in water, resulting in low bioavailability within the gastrointestinal tract, a key limitation for the effectiveness of many hydrophobic substances. In this study we developed a microemulsion-based drug delivery system in Drosophila, which effectively enhanced the solubility of hydrophobic compounds without noticeable effects on food intake or survival in fruit flies. This system consisted of cremophor EL, ethanol and ethyl oleate (7:6:1), which enabled the establishment of an emulsion-based liquid high-fat diet (LHFD) model, followed by a pilot screening of 161 standard substances from traditional Chinese medicine. We found that piperine (PIP), an alkaloid derived from black pepper, significantly decreased triacylglycerol (TAG) levels in both the intestine and in whole flies. We demonstrated that piperine (1 mg/ml) significantly elevated cytosolic Ca levels in enterocytes by activating Transient receptor potential (TRP) channels. TRPV1 agonists such as capsaicin and evodiamine (another alkaloid identified during the screening) also exhibited anti-obesity effects. Increased Ca levels resulted in the suppression of dietary lipase Magro expression through the activation of the transcription factor cAMP response element binding protein (CREB). Furthermore, hydrophobic compounds in the microemulsion were successfully delivered to distal tissues including liver and brain blood vessels in mice, and PIP in the microemulsion was sufficient to reduce body weight in mice. In conclusion, we have developed a microemulsion-based U-GLAD platform for drug delivery, and piperine is identified as a weight-controlling compound, providing a novel approach to the treatment of obesity and its associated symptoms.

摘要

肥胖是多种代谢性疾病(如心脏病和糖尿病)的重要促成因素。由于合成抗肥胖药物的副作用,来自功能性食用植物的天然产物,其模拟合成化学物质的作用,提供了有前景的替代方案。然而,许多天然植物衍生化合物在水中溶解度很差,导致在胃肠道内生物利用度低,这是许多疏水性物质有效性的关键限制。在本研究中,我们在果蝇中开发了一种基于微乳液的药物递送系统,其有效提高了疏水性化合物的溶解度,而对果蝇的食物摄入量或存活率没有明显影响。该系统由聚氧乙烯蓖麻油EL、乙醇和油酸乙酯(7:6:1)组成,能够建立基于乳液的液体高脂饮食(LHFD)模型,随后对161种中药标准物质进行初步筛选。我们发现胡椒碱(PIP),一种从黑胡椒中提取的生物碱,显著降低了肠道和整个果蝇中的三酰甘油(TAG)水平。我们证明胡椒碱(1mg/ml)通过激活瞬时受体电位(TRP)通道显著提高肠细胞中的胞质钙水平。TRPV1激动剂如辣椒素和吴茱萸碱(筛选过程中鉴定出的另一种生物碱)也表现出抗肥胖作用。钙水平升高导致通过激活转录因子cAMP反应元件结合蛋白(CREB)抑制膳食脂肪酶Magro的表达。此外,微乳液中的疏水性化合物成功递送至小鼠的远端组织,包括肝脏和脑血管,微乳液中的PIP足以减轻小鼠体重。总之,我们开发了一种基于微乳液的U-GLAD药物递送平台,并且胡椒碱被鉴定为一种体重控制化合物,为肥胖及其相关症状的治疗提供了一种新方法。

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