Hossain Sanowar, Yousaf Muhammad, Liu Yang, Chang Dennis, Zhou Xian
Department of Pharmacy, Pabna University of Science and Technology, Pabna, Bangladesh.
Department of Bioinformatics and Biotechnology, Government College University, Faisalabad, Pakistan.
Front Pharmacol. 2022 Apr 4;13:876183. doi: 10.3389/fphar.2022.876183. eCollection 2022.
With the growing interest in the medicinal use of propolis, numerous studies have reported significant interactions between propolis extract and pharmaceutical drugs which may result in great clinical benefits or risks. The present study aims to review the drug-herb interactions of the full-spectrum propolis extract and main pharmaceutical drugs from the pharmacodynamic and pharmacokinetic aspects and elucidate the underlying pharmacological mechanisms. A literature search was conducted between June 2021 and February 2022 in Google Scholar, PubMed, MEDLINE, and EMBASE databases to include English studies from years 2000 to 2022 that evaluated the interaction of full-spectrum propolis extract and standard pharmaceutical drugs/cytochromes P450s. Studies that looked into geopropolis, propolis fractions, and isolated compounds, or interaction of propolis with foods, bioactive molecules, or receptors other than standard pharmaceutical drugs were excluded. From a pharmacodynamic perspective, propolis extract exhibited positive or synergistic interaction with several chemotherapeutic drugs by enhancing antitumor activity, sensitizing the chemoresistance cell lines, and attenuating multi-organ toxicity. The molecular mechanisms were associated with upregulating the apoptotic signal and immunomodulatory activity and attenuating oxidative damage. Propolis extract also enhanced the anti-bacterial and antifungal activities of many antimicrobial drugs against sensitive and resistant organisms, with an effect against the gram-positive bacteria stronger than that of the gram-negative bacteria. The synergistic action was related to strengthened action on interfering cell wall integrity and protein synthesis. The strong antioxidant activity of propolis also strengthened the therapeutic effect of metformin in attenuating hyperglycemia and pancreatic damage, as well as mitigating oxidative stress in the liver, kidney, and testis. In addition, propolis showed a potential capacity to enhance short-term and long-term memory function together with donepezil and improve motor function with levodopa and parasite killing activity with praziquantel. Pharmacokinetic studies showed inhibitory activities of propolis extracts on several CYP450 enzymes and . However, the effects on those CYP450 were deemed insignificant in humans, which may be attributed to the low bioavailability of the contributing bioactive compounds when administered in the body. The enhanced bioactivities of propolis and main pharmaceutical drugs support using propolis in integrative medicine in anti-cancer, anti-microbial, antidiabetic, and neurological disorders, with a low risk of altered pharmacokinetic activities.
随着人们对蜂胶药用价值的兴趣日益浓厚,众多研究报告了蜂胶提取物与药物之间存在显著相互作用,这可能带来巨大的临床益处或风险。本研究旨在从药效学和药代动力学方面综述全谱蜂胶提取物与主要药物之间的药物 - 草药相互作用,并阐明其潜在的药理机制。于2021年6月至2022年2月在谷歌学术、PubMed、MEDLINE和EMBASE数据库中进行文献检索,纳入2000年至2022年评估全谱蜂胶提取物与标准药物/细胞色素P450相互作用的英文研究。排除研究地蜂胶、蜂胶馏分和分离化合物,或蜂胶与食物、生物活性分子或除标准药物之外的受体相互作用的研究。从药效学角度来看,蜂胶提取物通过增强抗肿瘤活性、使化疗耐药细胞系敏感化以及减轻多器官毒性,与多种化疗药物表现出正向或协同相互作用。其分子机制与上调凋亡信号和免疫调节活性以及减轻氧化损伤有关。蜂胶提取物还增强了许多抗菌药物对敏感和耐药菌的抗菌和抗真菌活性,对革兰氏阳性菌的作用强于革兰氏阴性菌。协同作用与加强干扰细胞壁完整性和蛋白质合成的作用有关。蜂胶强大的抗氧化活性还增强了二甲双胍在减轻高血糖和胰腺损伤以及减轻肝脏、肾脏和睾丸氧化应激方面的治疗效果。此外,蜂胶显示出与多奈哌齐一起增强短期和长期记忆功能、与左旋多巴改善运动功能以及与吡喹酮杀灭寄生虫活性的潜在能力。药代动力学研究表明蜂胶提取物对几种CYP450酶有抑制活性。然而,对这些CYP450的影响在人体中被认为不显著,这可能归因于相关生物活性化合物在体内给药时生物利用度较低。蜂胶与主要药物增强的生物活性支持在综合医学中使用蜂胶治疗癌症、抗菌、抗糖尿病和神经系统疾病,药代动力学活性改变的风险较低。