Huang Yi-Ning, Hsu Chien-Ning, Hou Chih-Yao, Chen Shin-Yu, Tain You-Lin
Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Department of Pharmacy, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Nutrients. 2024 Nov 27;16(23):4076. doi: 10.3390/nu16234076.
Resveratrol is recognized as a promising nutraceutical with antihypertensive and prebiotic properties; however, its bioavailability in vivo is limited. To enhance its bioactivity, we developed resveratrol butyrate esters (RBEs). This study investigates whether RBEs can mitigate hypertension induced by chronic kidney disease (CKD) and exacerbated by microplastics (MPs) exposure in juvenile rats.
Three-week-old male Sprague Dawley rats were fed either regular chow or 0.5% adenine chow for three weeks. The adenine-fed CKD rats (N = 8 per group) received either 5 μM MPs (10 mg/L) or MPs combined with RBE (25 mg/L) in their drinking water from weeks 3 to 9.
Our results indicate that MP exposure worsened CKD-induced hypertension, while RBE treatment resulted in a reduction in systolic BP by 15 mmHg (155 ± 2 mmHg vs. 140 ± 1 mmHg, < 0.05). The combined exposure to adenine and MPs was associated with nitric oxide (NO) deficiency, which RBE treatment alleviated. Additionally, our findings revealed that RBE modulated both the classical and nonclassical renin-angiotensin system (RAS), contributing to its protective effects. We also observed changes in gut microbiota composition, increased butyric acid levels, and elevated renal GPR41 expression associated with RBE treatment.
In conclusion, in this juvenile rat model of combined CKD and MP exposure, RBE demonstrates antihypertensive effects by modulating NO levels, the RAS, gut microbiota, and their metabolites.
白藜芦醇被认为是一种具有抗高血压和益生元特性的有前景的营养保健品;然而,其体内生物利用度有限。为提高其生物活性,我们开发了白藜芦醇丁酸酯(RBEs)。本研究调查RBEs是否能减轻幼年大鼠由慢性肾脏病(CKD)诱导并因微塑料(MPs)暴露而加剧的高血压。
给3周龄雄性斯普拉格-道利大鼠喂食普通饲料或含0.5%腺嘌呤的饲料,持续3周。从第3周开始至第9周,给喂食腺嘌呤的CKD大鼠(每组8只)的饮用水中添加5 μM MPs(10 mg/L)或MPs与RBE(25 mg/L)的混合物。
我们的结果表明,MPs暴露使CKD诱导的高血压恶化,而RBE治疗使收缩压降低了15 mmHg(155±2 mmHg对140±1 mmHg,P<0.05)。腺嘌呤和MPs联合暴露与一氧化氮(NO)缺乏有关,而RBE治疗减轻了这种缺乏。此外,我们的研究结果显示,RBE调节了经典和非经典肾素-血管紧张素系统(RAS),从而产生其保护作用。我们还观察到肠道微生物群组成的变化、丁酸水平的升高以及与RBE治疗相关的肾脏GPR41表达的升高。
总之,在这个CKD和MPs暴露联合的幼年大鼠模型中,RBE通过调节NO水平、RAS、肠道微生物群及其代谢产物发挥抗高血压作用。