Department of Physiology and Pharmacology, Center for Hypertension and Personalized Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
Am J Physiol Heart Circ Physiol. 2022 Mar 1;322(3):H466-H473. doi: 10.1152/ajpheart.00486.2021. Epub 2022 Feb 11.
With an aging global population, identifying novel therapeutics are necessary to increase longevity and decrease the deterioration of essential end organs such as the vasculature. Secondary alcohol, 1,3-butanediol (1,3-BD), is commonly administered to stimulate the biosynthesis of the most abundant ketone body β-hydroxybutyrate (βHB), in lieu of nutrient deprivation. However, suprapharmacological concentrations of 1,3-BD are necessary to significantly increase systemic βHB, and 1,3-BD per se can cause vasodilation at nanomolar concentrations. Therefore, we hypothesized that 1,3-BD could be a novel antiaging therapeutic, independent of βHB biosynthesis. To test this hypothesis, we administered a low-dose (5%) 1,3-BD to young and old Wistar-Kyoto (WKY) rats via drinking water for 4 wk and measured indices of vascular function and metabolism posttreatment. We observed that low-dose 1,3-BD was sufficient to reverse age-associated endothelial-dependent and -independent dysfunction, and this was not associated with increased βHB bioavailability. Further analysis of the direct vasodilator mechanisms of 1,3-BD revealed that it is predominantly an endothelium-dependent vasodilator through activation of potassium channels and nitric oxide synthase. In summary, we report that 1,3-BD, at a concentration that does not stimulate βHB biosynthesis, could be a nutraceutical that can reverse the age-associated decline in vascular function. These results emphasize that 1,3-BD has multiple, concentration-dependent mechanisms of action. Therefore, we suggest alternative approaches to study the physiological and cardiovascular effects of βHB. 1,3-Butanediol (1,3-BD) is often administered to stimulate the biosynthesis of the most abundant ketone body, β-hydroxybutyrate (βHB), and its purported salubrious effects. Here, we report that a low dose of 1,3-BD (5%) is sufficient to reverse age-associated vascular dysfunction, independent of βHB. Therefore, low-dose 1,3-BD could be a novel therapeutic to increase blood flow and improve the quality of life in the elderly.
随着全球人口老龄化,有必要寻找新的治疗方法来延长寿命并减缓血管等重要器官的恶化。1,3-丁二醇(1,3-BD)是一种常用的药物,可用于刺激最丰富的酮体β-羟基丁酸(βHB)的生物合成,以代替营养剥夺。然而,需要超药理学浓度的 1,3-BD 才能显著增加系统中的βHB,而 1,3-BD 本身在纳摩尔浓度下就可以引起血管扩张。因此,我们假设 1,3-BD 可以作为一种独立于βHB 生物合成的新型抗衰老治疗方法。为了验证这一假设,我们通过饮用水向年轻和年老的 Wistar-Kyoto(WKY)大鼠给予低剂量(5%)的 1,3-BD,持续 4 周,并在治疗后测量血管功能和代谢的指标。我们观察到,低剂量的 1,3-BD 足以逆转与年龄相关的内皮依赖性和非依赖性功能障碍,并且这与增加的βHB 生物利用度无关。对 1,3-BD 的直接血管扩张机制的进一步分析表明,它主要是一种通过激活钾通道和一氧化氮合酶的内皮依赖性血管扩张剂。总之,我们报告说,1,3-BD 可以在不刺激βHB 生物合成的浓度下,作为一种营养保健品,逆转与年龄相关的血管功能下降。这些结果强调了 1,3-BD 具有多种浓度依赖性作用机制。因此,我们建议采用替代方法来研究βHB 的生理和心血管作用。1,3-丁二醇(1,3-BD)常被用于刺激最丰富的酮体β-羟基丁酸(βHB)的生物合成,以及其据称的有益作用。在这里,我们报告低剂量的 1,3-BD(5%)足以逆转与年龄相关的血管功能障碍,而与βHB 无关。因此,低剂量的 1,3-BD 可能是一种新的治疗方法,可以增加老年人的血流量并提高生活质量。