Effects of Combined Exercise Training on Modulating Fine Particulate Matter–Induced Skeletal Muscle Damage in Offspring Gestationally Exposed

IF 9.1 1区 医学 Q1 GERIATRICS & GERONTOLOGY
Zilin Wang, Wenduo Liu, Hyun-Jaung Sim, Jeong-Chae Lee, Sung-Ho Kook, Sang Hyun Kim
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Abstract

Background

Fine particulate matter has developmental toxicity, and midgestation is an important period for the development of foetal skeletal muscle. The ability of exercise to modulate skeletal muscle damage in mice exposed to PM2.5 during gestation remains unclear.

Methods

Pregnant C57BL/6 mice were exposed to 50 μg/m3 PM2.5 for 2 h on five consecutive days starting at embryonic day 12.5 (E12.5d). Combined exercise (treadmill endurance training and weighted ladder resistance training) was followed for 8 weeks in the 4-week-old offspring to verify the regulatory effect of exercise.

Results

Offspring exposed to PM2.5 during gestation showed lower body weight (male, −44.3%; female, −44.8%; p < 0.001), lower skeletal muscle mass (male: TA fibre size, −42%, p < 0.001; TA mass, −37%, p < 0.01; gastrocnemius mass, −46.5%, p < 0.001; female: TA fibre size, −51.6%, p < 0.001; TA mass, −29.8%, p < 0.05; gastrocnemius mass, −40.7%, p < 0.01) and mitochondrial (size decreased for TEM; male: PGC-1α, +78.1%, p < 0.05; Tfam, +591.3%, p < 0.001; FIS-1, +627%, p < 0.001; female: Tfam, +452%, p < 0.01; FIS-1, +345.6%, p < 0.01) dysfunction (at 4 weeks old). They also showed catch-up growth (between 3 and 8 weeks of age; male average weight gain level, +57.9%, p < 0.01; female average weight gain level, +66%, p < 0.05), although they still showed significant mitochondrial damage and impaired glucose metabolism (at 13 weeks of age; male: mitochondrial damage for TEM; Tfam, −46%, p < 0.01; PINK-1, −33.8%, p < 0.05; Parkin, −62%, p < 0.01; PFK-1, −17%, p < 0.05; female: mitochondrial damage for TEM; PFK-1, −28.7%, p < 0.01). Combined exercise was unable to regulate the skeletal muscle system disorder that occurred in male offspring exposed to PM2.5 during pregnancy. However, it activated the mitophagy (PINK-1, +94.6%, p < 0.05; Parkin, +90.2%, p < 0.001) in female offspring exposed to PM2.5 during pregnancy, thereby improving mitochondrial damage.

Conclusions

Combined exercise had bidirectional, sex-specific effects: Male offspring exhibited reduced responsiveness to exercise, with persistent mitochondrial damage, whereas female offspring showed improved mitochondrial health through increased mitophagy flux.

Abstract Image

联合运动训练对妊娠期接触细颗粒物子代骨骼肌损伤的调节作用
细颗粒物具有发育毒性,妊娠中期是胎儿骨骼肌发育的重要时期。在妊娠期暴露于PM2.5的小鼠中,运动调节骨骼肌损伤的能力尚不清楚。方法C57BL/6妊娠小鼠从胚胎第12.5天(E12.5d)开始,连续5天暴露于50 μg/m3 PM2.5环境2 h。对4周龄幼鼠进行8周的联合运动(跑步机耐力训练和加权阶梯阻力训练),验证运动的调节作用。结果妊娠期暴露于PM2.5的子代体重降低(雄性为- 44.3%,雌性为- 44.8%,p < 0.001),骨骼肌质量降低(雄性:TA纤维大小为- 42%,p < 0.001; TA质量为- 37%,p < 0.01;腓肠肌质量为- 46.5%,p < 0.001;雌性:TA纤维大小为- 51.6%,p < 0.001; TA质量为- 29.8%,p < 0.05;腓肠肌质量为- 40.7%,p < 0.01),线粒体(TEM尺寸减小;雄性:PGC-1α, +78.1%, p < 0.05;Tfam, +591.3%, p < 0.001;fis1, +627%, p < 0.001;女:Tfam, +452%, p < 0.01;FIS-1, +345.6%, p < 0.01)功能障碍(4周龄)。他们还显示追赶生长(年龄3至8周;男性平均体重水平,+ 57.9%,p & lt; 0.01;女性平均体重水平,+ 66%,p & lt; 0.05),尽管他们仍然显示显著的线粒体损伤和葡萄糖代谢(年龄在13周;男:TEM线粒体损伤;Tfam,−46%,p & lt; 0.01;粉1,−33.8%,p & lt; 0.05;帕金,−62%,p & lt; 0.01; PFK-1,−17%,p & lt; 0.05;女:TEM线粒体损伤;PFK-1,−28.7%,p & lt; 0.01)。联合运动无法调节在怀孕期间暴露于PM2.5的雄性后代发生的骨骼肌系统紊乱。然而,它激活了怀孕期间暴露于PM2.5的雌性后代的线粒体自噬(PINK-1, +94.6%, p < 0.05; Parkin, +90.2%, p < 0.001),从而改善了线粒体损伤。结论:联合运动具有双向的、性别特异性的影响:雄性后代对运动的反应性降低,线粒体持续损伤,而雌性后代通过增加线粒体自噬通量,线粒体健康得到改善。
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来源期刊
Journal of Cachexia Sarcopenia and Muscle
Journal of Cachexia Sarcopenia and Muscle MEDICINE, GENERAL & INTERNAL-
CiteScore
13.30
自引率
12.40%
发文量
234
审稿时长
16 weeks
期刊介绍: The Journal of Cachexia, Sarcopenia and Muscle is a peer-reviewed international journal dedicated to publishing materials related to cachexia and sarcopenia, as well as body composition and its physiological and pathophysiological changes across the lifespan and in response to various illnesses from all fields of life sciences. The journal aims to provide a reliable resource for professionals interested in related research or involved in the clinical care of affected patients, such as those suffering from AIDS, cancer, chronic heart failure, chronic lung disease, liver cirrhosis, chronic kidney failure, rheumatoid arthritis, or sepsis.
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