Kawaida Mia Y, Kwon Oh Sung, Ahn Ahram, Reiter Amanda S, Tillquist Nicole M, Noh Sung Gi, Lee Jung W, Moore Timothy E, Reed Sarah A
Department of Animal Science, University of Connecticut, Storrs, Connecticut, USA.
Department of Kinesiology, University of Connecticut, Storrs, Connecticut, USA.
Physiol Rep. 2025 Apr;13(8):e70346. doi: 10.14814/phy2.70346.
This study investigated the effects of astaxanthin (ASTX) supplementation on oxidative status during a deconditioning-reconditioning cycle. Twelve polo ponies were assigned to no supplementation (CON) or an ASTX supplemented group, which received oral administration of a supplement containing 75 mg ASTX daily for 32 weeks. Polo ponies underwent a 16-week deconditioning period (DECON) followed by a 16-week reconditioning program (RECON). Submaximal exercise tests (SETs) were performed at the beginning of the study (Baseline), after DECON, and after RECON. Blood samples were collected at -30, 0, 15, 30, and 60 min relative to each SET for oxidative status analysis. Muscle samples were collected 2 weeks before (Pre-Ex) and 2 h after (Post-Ex) each SET for muscle oxidative status and gene expression analyses. Pre-Ex muscles were analyzed for high-resolution respirometry. Circulating glutathione peroxidase (GPX) activity was increased (p ≤ 0.02) and protein carbonylation was decreased in ASTX (p ≤ 0.05). Muscle oxidative status was affected by DECON and reconditioning (p ≤ 0.05). ASTX increased gene expression of PPARGC1A after reconditioning (p ≤ 0.05). Deconditioning reduced oxidative phosphorylation at complex I and II (p = 0.01). Thus, a deconditioning-reconditioning cycle had greater impacts on muscle oxidative capacity than ASTX supplementation.
本研究调查了补充虾青素(ASTX)对去适应 - 再适应周期中氧化状态的影响。将12匹马球用马分为不补充组(CON)和ASTX补充组,后者每天口服含75毫克ASTX的补充剂,持续32周。马球用马经历了16周的去适应期(DECON),随后是16周的再适应计划(RECON)。在研究开始时(基线)、DECON后和RECON后进行次最大运动测试(SET)。在每次SET相对应的 -30、0、15、30和60分钟采集血样用于氧化状态分析。在每次SET前2周(运动前)和后2小时(运动后)采集肌肉样本用于肌肉氧化状态和基因表达分析。对运动前的肌肉进行高分辨率呼吸测定分析。ASTX组循环谷胱甘肽过氧化物酶(GPX)活性增加(p≤0.02),蛋白质羰基化减少(p≤0.05)。肌肉氧化状态受去适应和再适应影响(p≤0.05)。再适应后ASTX增加了PPARGC1A的基因表达(p≤0.05)。去适应降低了复合体I和II处的氧化磷酸化(p = 0.01)。因此,去适应 - 再适应周期对肌肉氧化能力的影响大于补充ASTX。