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抗氧化补充剂作为一种新型手段,可阻断含果糖饮料再水化后反复热应激引起的肾脏损伤。

Antioxidant supplements as a novel mean for blocking recurrent heat stress-induced kidney damage following rehydration with fructose-containing beverages.

机构信息

Lab. Renal Physiopathology, Dept. of Nephrology, INC Ignacio Chávez. Mexico City, Mexico.

Danone Research, Palaiseau, France.

出版信息

Free Radic Biol Med. 2019 Sep;141:182-191. doi: 10.1016/j.freeradbiomed.2019.06.016. Epub 2019 Jun 15.

Abstract

Recently repeated heat stress and dehydration have been reported to cause oxidative stress and kidney damage that is enhanced by rehydrating with fructose solutions. We hypothesized that antioxidants might provide a novel way to prevent kidney damage. To test this hypothesis, mild heat stress was induced by exposing rats to 37 °C during 1 h in a closed chamber. The supplementation with water-soluble antioxidants (Antiox), ascorbic acid 1% plus N-acetyl cysteine 600 mg/L was done either in the 10% fructose 2 h rehydration fluid immediately after heat stress (Fructose 10% + Antiox), and/or in the tap water (Water + Antiox) for the remainder of the day, or in both fluids. After 4 weeks, control rats exposed to heat with fructose rehydration developed impaired renal function, tubular injury, intrarenal oxidative stress, a reduction in Nrf2-Keap1 antioxidant pathway, stimulation of vasopressin and the intrarenal polyol-fructokinase pathway. In contrast, dosing the antioxidants in the tap water (i.e., before the heat exposure and rehydration with fructose) preserved renal function, prevented renal tubule dysfunction and avoided the increase in systemic blood pressure. These effects were likely due to the amplification of the antioxidant defenses through increased Nrf2 nuclear translocation stimulated by the antioxidants and by the prevention of polyol fructokinase pathway overactivation. More studies to understand the mechanisms implicated in this pathology are warranted as there is recent evidence that they may be operating in humans as well.

摘要

最近有报道称,反复的热应激和脱水会导致氧化应激和肾脏损伤,而用果糖溶液进行补液会加重这种损伤。我们假设抗氧化剂可能提供一种预防肾脏损伤的新方法。为了验证这一假设,我们通过将大鼠置于封闭室中 37°C 下 1 小时来诱导轻度热应激。在热应激后立即用 10%果糖 2 小时补液液(果糖 10%+Antiox)和/或在自来水(水+Antiox)中补充水溶性抗氧化剂(Antiox)、抗坏血酸 1%加 N-乙酰半胱氨酸 600mg/L,持续一天,或在两种液体中补充。4 周后,暴露于热应激和果糖补液的对照组大鼠出现肾功能受损、肾小管损伤、肾内氧化应激、Nrf2-Keap1 抗氧化途径减少、血管加压素刺激和肾内多元醇-果糖激酶途径激活。相比之下,在自来水中补充抗氧化剂(即在暴露于热应激和用果糖补液之前)可以保护肾功能,防止肾小管功能障碍,并避免全身血压升高。这些作用可能是由于抗氧化剂刺激 Nrf2 核易位,增加抗氧化防御,以及防止多元醇果糖激酶途径过度激活,从而增强了抗氧化防御。需要进一步研究以了解该病理学中涉及的机制,因为最近有证据表明,这些机制在人类中也可能起作用。

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