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通过脑靶向递送载咖啡因转铁蛋白脂质体提高SD大鼠的身体机能。

Boosting physical performance in SD rats through brain-targeted delivery of caffeine-loaded transferrin liposomes.

作者信息

Yun Hezhang, Su Wenbo, You Ting, Wang Jing, Ying Yuxuan, Wang Can, Ren Yuyi, Lu Bin, Li Yi, Liu Chang

机构信息

School of Physical Education, Zhejiang Guangsha Vocational and Technical University of Construction, Dongyang, 322100, China.

School of Sport Science, Beijing Sport University, Beijing, 100084, China.

出版信息

Heliyon. 2024 Jul 14;10(14):e34617. doi: 10.1016/j.heliyon.2024.e34617. eCollection 2024 Jul 30.

DOI:10.1016/j.heliyon.2024.e34617
PMID:39114047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11305279/
Abstract

This study aimed to explore the impact of caffeine (CAF) encapsulated in transferrin-modified, sterically-stabilized liposomes (Tf-SSL) on the physical performance of rats, specifically forelimb grip strength, running, and swimming. The brain-targeted drug delivery system, Tf-SSL, was used for the administration of caffeine. 168 male Sprague-Dawley (SD) rats were randomly assigned to different groups, including swimming, running, running wheel, and strength groups. Each group was further subdivided into high, medium, and low dose free caffeine (HCAF, MCAF, LCAF) and Tf-SSL CAF groups, along with a control group (CON). The strength, swimming, and running groups underwent training for four weeks, three times per week. The running wheel group was placed in rearing cages for a one-week adaptation period. After the final training session, the resistance, swimming, running, and running wheel exercise capacities of the rats were tested. The rats were administered treatment via tail vein injection, while the blank CON group received 0.9 % saline solution without treatment throughout the entire process. The results demonstrated a Tf-SSL CAF group encapsulation rate of 70.58 ± 5.14 %. Increasing the concentration of supplemented caffeine led to enhanced forelimb grip strength in rats, with significant differences observed in HCAF alone group, medium-dose Tf-SSL CAF (MTf-SSL CAF), and high-dose Tf-SSL CAF (HTf-SSL CAF) groups compared to the CON group. In the running and swimming experiments, higher caffeine supplementation concentrations correlated with increased running and swimming time to exhaustion, and the MTf-SSL CAF group showed longer running and swimming time compared to the HCAF alone group. The results of rat striatal dopamine levels indicated that increased caffeine supplementation concentrations led to higher dopamine secretion, with significantly different striatal concentrations in the HCAF group, MTf-SSL CAF group, and HTf-SSL CAF group compared to the CON group. The running wheel experiment revealed that rats in the medium- and high-dose Tf-SSL CAF groups exhibited greater 6-h running distances than the HCAF group and CON group. In conclusion, caffeine supplementation improved the physical performance of rats, with the high concentration CAF group outperforming the low and medium concentration groups. Furthermore, Tf-SSL CAF demonstrated superior physical enhancement compared to caffeine supplementation alone.

摘要

本研究旨在探讨包裹于转铁蛋白修饰的空间稳定脂质体(Tf-SSL)中的咖啡因(CAF)对大鼠身体机能的影响,具体包括前肢握力、跑步和游泳能力。采用脑靶向给药系统Tf-SSL来给予咖啡因。168只雄性Sprague-Dawley(SD)大鼠被随机分为不同组,包括游泳组、跑步组、跑轮组和力量组。每组又进一步细分为高、中、低剂量游离咖啡因(HCAF、MCAF、LCAF)组和Tf-SSL CAF组,以及一个对照组(CON)。力量组、游泳组和跑步组进行为期四周的训练,每周三次。跑轮组置于饲养笼中进行为期一周的适应期。在最后一次训练 session 后,测试大鼠的耐力、游泳、跑步和跑轮运动能力。通过尾静脉注射给予大鼠治疗,而空白CON组在整个过程中接受0.9%生理盐水溶液,不进行治疗。结果显示Tf-SSL CAF组的包封率为70.58±5.14%。增加补充咖啡因的浓度可提高大鼠的前肢握力,与CON组相比,单独的HCAF组、中剂量Tf-SSL CAF(MTf-SSL CAF)组和高剂量Tf-SSL CAF(HTf-SSL CAF)组观察到显著差异。在跑步和游泳实验中,较高的咖啡因补充浓度与增加的跑步和游泳至力竭时间相关,并且MTf-SSL CAF组的跑步和游泳时间比单独的HCAF组长。大鼠纹状体多巴胺水平的结果表明,增加咖啡因补充浓度会导致更高的多巴胺分泌,与CON组相比,HCAF组、MTf-SSL CAF组和HTf-SSL CAF组的纹状体浓度有显著差异。跑轮实验表明,中、高剂量Tf-SSL CAF组的大鼠在6小时内的跑步距离比HCAF组和CON组更长。总之,补充咖啡因可改善大鼠的身体机能,高浓度CAF组优于低浓度和中浓度组。此外,与单独补充咖啡因相比,Tf-SSL CAF表现出更优异的身体机能增强效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/d0b44302312f/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/ede539f37459/gr1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/aef91ba7b495/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/624d0e456a17/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/133d5f73da54/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/d0b44302312f/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/ede539f37459/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/33700e22134d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/aef91ba7b495/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/624d0e456a17/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/133d5f73da54/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/11305279/d0b44302312f/gr6.jpg

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