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生长育肥公猪急性热应激挑战期间米托醌的治疗效果。

Therapeutic effects of mitoquinol during an acute heat stress challenge in growing barrows.

机构信息

Department of Animal Science, Iowa State University, Ames, IA 50011, USA.

Department of Animal and Poultry Sciences, Virginia Tech, Blacksburg, VA 24061, USA.

出版信息

J Anim Sci. 2024 Jan 3;102. doi: 10.1093/jas/skae161.

DOI:10.1093/jas/skae161
PMID:38860702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11208932/
Abstract

Study objectives were to determine the effects of mitoquinol (MitoQ, a mitochondrial-targeted antioxidant) on biomarkers of metabolism and inflammation during acute heat stress (HS). Crossbred barrows [n = 32; 59.0 ± 5.6 kg body weight (BW)] were blocked by BW and randomly assigned to 1 of 4 environmental-therapeutic treatments: 1) thermoneutral (TN) control (n = 8; TNCon), 2) TN and MitoQ (n = 8; TNMitoQ), 3) HS control (n = 8; HSCon), or 4) HS and MitoQ (n = 8; HSMitoQ). Pigs were acclimated for 6 d to individual pens before study initiation. The trial consisted of two experimental periods (P). During P1 (2 d), pigs were fed ad libitum and housed in TN conditions (20.6 ± 0.8 °C). During P2 (24 h), HSCon and HSMitoQ pigs were exposed to continuous HS (35.2 ± 0.2 °C), while TNCon and TNMitoQ remained in TN conditions. MitoQ (40 mg/d) was orally administered twice daily (0700 and 1800 hours) during P1 and P2. Pigs exposed to HS had increased rectal temperature, skin temperature, and respiration rate (+1.5 °C, +6.8 °C, and +101 breaths per minute, respectively; P < 0.01) compared to their TN counterparts. Acute HS markedly decreased feed intake (FI; 67%; P < 0.01); however, FI tended to be increased in HSMitoQ relative to HSCon pigs (1.5 kg vs. 0.9 kg, respectively; P = 0.08). Heat-stressed pigs lost BW compared to their TN counterparts (-4.7 kg vs. +1.6 kg, respectively; P < 0.01); however, the reduction in BW was attenuated in HSMitoQ compared to HSCon pigs (-3.9 kg vs. -5.5 kg, respectively; P < 0.01). Total gastrointestinal tract weight (empty tissue and luminal contents) was decreased in HS pigs relative to their TN counterparts (6.2 kg vs. 8.6 kg, respectively; P < 0.01). Blood glucose increased in HSMitoQ relative to HSCon pigs (15%; P = 0.04). Circulating non-esterified fatty acids (NEFA) increased in HS compared to TN pigs (P < 0.01), although this difference was disproportionately influenced by elevated NEFA in HSCon relative to HSMitoQ pigs (251 μEq/L vs. 142 μEq/L; P < 0.01). Heat-stressed pigs had decreased circulating insulin relative to their TN counterparts (47%; P = 0.04); however, the insulin:FI ratio tended to increase in HS relative to TN pigs (P = 0.09). Overall, circulating leukocytes were similar across treatments (P > 0.10). Plasma C-reactive protein remained similar among treatments; however, haptoglobin increased in HS relative to TN pigs (48%; P = 0.03). In conclusion, acute HS exposure negatively altered animal performance, inflammation, and metabolism, which were partially ameliorated by MitoQ.

摘要

研究目的是确定米托醌(MitoQ,一种靶向线粒体的抗氧化剂)对急性热应激(HS)期间代谢和炎症生物标志物的影响。杂交公猪[n = 32;59.0 ± 5.6 kg 体重(BW)]按 BW 分组并随机分配到 4 种环境治疗处理之一:1) 常温对照(TNCon),2) 常温+MitoQ(TNMitoQ),3) HS 对照(HSCon),或 4) HS+MitoQ(HSMitoQ)。猪在开始研究前适应了 6 天的个体围栏。试验包括两个实验期(P)。在 P1(2 天)期间,猪自由采食并在 TN 条件下饲养(20.6 ± 0.8°C)。在 P2(24 小时)期间,HSCon 和 HSMitoQ 猪持续暴露于 HS(35.2 ± 0.2°C),而 TNCon 和 TNMitoQ 则保持在 TN 条件下。MitoQ(40mg/d)在 P1 和 P2 期间每天口服两次(0700 和 1800 小时)。与 TN 对应物相比,暴露于 HS 的猪的直肠温度、皮肤温度和呼吸率分别升高了 1.5°C、6.8°C 和 101 次/分钟(P < 0.01)。急性 HS 显著降低了采食量(FI;67%;P < 0.01);然而,与 HSCon 猪相比,HSMitoQ 猪的 FI 趋于增加(分别为 1.5 kg 和 0.9 kg;P = 0.08)。与 TN 对应物相比,HS 应激猪的 BW 减轻(分别为-4.7 kg 和+1.6 kg;P < 0.01);然而,与 HSCon 猪相比,HSMitoQ 猪 BW 的减少量减少(分别为-3.9 kg 和-5.5 kg;P < 0.01)。与 TN 对应物相比,总胃肠道重量(空组织和腔内容物)减少(分别为 6.2 kg 和 8.6 kg;P < 0.01)。与 HSCon 猪相比,HSMitoQ 猪的血糖升高(15%;P = 0.04)。与 TN 猪相比,循环非酯化脂肪酸(NEFA)在 HS 中增加(P < 0.01),尽管 HSCon 猪的 NEFA 升高不成比例地影响了 HSMitoQ 猪(251 μEq/L 和 142 μEq/L;P < 0.01)。与 TN 对应物相比,HS 应激猪的循环胰岛素减少(47%;P = 0.04);然而,与 TN 猪相比,HS 猪的胰岛素:FI 比值趋于增加(P = 0.09)。总的来说,循环白细胞在处理之间相似(P > 0.10)。血浆 C 反应蛋白在处理之间保持相似;然而,与 TN 猪相比,触珠蛋白增加(48%;P = 0.03)。总之,急性 HS 暴露对动物性能、炎症和代谢产生了负面影响,这些负面影响部分被 MitoQ 减轻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d39/11208932/0cb33ea79ae8/skae161_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d39/11208932/e4d9f170ee9d/skae161_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d39/11208932/0cb33ea79ae8/skae161_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d39/11208932/e4d9f170ee9d/skae161_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d39/11208932/0cb33ea79ae8/skae161_fig2.jpg

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