Changes in serial sarcomere number of five hindlimb muscles across adult aging in rats.

IF 3.1 3区 医学 Q3 GERIATRICS & GERONTOLOGY
Gerontology Pub Date : 2025-06-22 DOI:10.1159/000546887
Avery Hinks, Geoffrey A Power
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引用次数: 0

Abstract

Introduction: The age-associated loss of muscle mass is partly accounted for by a reduction in muscle fascicle length (FL). Studies on rodents have confirmed this reduced FL is driven by a loss of sarcomeres aligned in series (serial sarcomere number; SSN) along a muscle. However, studies on rodents have focused primarily on rat plantar flexor SSN at two aging timepoints, leaving an incomplete view of age-related changes in SSN. Hence, this study investigated SSN as a contributor to the age-related loss of muscle mass in five hindlimb muscles across four aging timepoints in rats.

Methods: The soleus, medial gastrocnemius (MG), plantaris, tibialis anterior (TA), and vastus lateralis (VL) were obtained from 5 young (8 months), 5 middle-aged (20 months), 5 old (32 months), and 5 very old (36 months) male F344BN rats. After fixation of muscles in formalin and digestion in nitric acid, fascicles were teased out end-to-end to measure FL. SSN was determined by dividing FL by sarcomere length measured via laser diffraction. Muscle wet weight, anatomical cross-sectional area (ACSA), and physiological cross-sectional area (PCSA) were also determined for insight on age-related losses of whole-muscle mass and in-parallel muscle morphology.

Results: Age-related SSN loss was apparent after middle age for all muscles, with the plantaris showing the smallest (8%) and the VL the greatest (21%) differences between age groups. The MG and VL appeared to plateau in their SSN loss by 32 months, while the soleus and TA demonstrated continued decline from 32 to 36 months. In all muscles, an age-related lower SSN evidently contributed in part to the smaller muscle mass, alongside less contractile tissue in parallel (indicated by ACSA and PCSA).

Conclusion: As SSN is closely tied to biomechanical function, these findings present SSN as a distinct target for improving muscle performance in older adults.

成年大鼠后肢5块肌肉系列肌节数随衰老的变化。
简介:与年龄相关的肌肉质量损失部分是由肌肉束长度(FL)的减少引起的。对啮齿动物的研究已经证实,FL的减少是由排列成系列的肌节(serial sarcomere number;(SSN)沿着肌肉。然而,对啮齿动物的研究主要集中在两个衰老时间点的大鼠足底屈肌SSN,对SSN的年龄相关变化留下了不完整的看法。因此,本研究调查了SSN在大鼠四个衰老时间点的五块后肢肌肉中与年龄相关的肌肉质量损失。方法:选取5只幼年(8个月)、5只中年(20个月)、5只老年(32个月)、5只特高龄(36个月)雄性f3440大鼠,取比目鱼肌、腓肠肌内侧(MG)、足底肌、胫骨前肌(TA)、股外侧肌(VL)。将肌肉在福尔马林中固定并在硝酸中消化后,端到端梳理肌束来测量FL。SSN通过激光衍射测量的肌节长度除以FL来确定。还测定了肌肉湿重、解剖横截面积(ACSA)和生理横截面积(PCSA),以了解与年龄相关的全肌肉质量损失和平行肌肉形态。结果:年龄相关的SSN在中年后所有肌肉都明显下降,足底肌在年龄组之间的差异最小(8%),VL最大(21%)。MG和VL的SSN损失在32个月时趋于平稳,而比目鱼和TA在32至36个月期间持续下降。在所有肌肉中,与年龄相关的较低的SSN明显部分地导致了较小的肌肉质量,同时也导致了较少的收缩组织(由ACSA和PCSA显示)。结论:由于SSN与生物力学功能密切相关,这些发现表明SSN是改善老年人肌肉表现的一个独特目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gerontology
Gerontology 医学-老年医学
CiteScore
6.00
自引率
0.00%
发文量
94
审稿时长
6-12 weeks
期刊介绍: In view of the ever-increasing fraction of elderly people, understanding the mechanisms of aging and age-related diseases has become a matter of urgent necessity. ''Gerontology'', the oldest journal in the field, responds to this need by drawing topical contributions from multiple disciplines to support the fundamental goals of extending active life and enhancing its quality. The range of papers is classified into four sections. In the Clinical Section, the aetiology, pathogenesis, prevention and treatment of agerelated diseases are discussed from a gerontological rather than a geriatric viewpoint. The Experimental Section contains up-to-date contributions from basic gerontological research. Papers dealing with behavioural development and related topics are placed in the Behavioural Science Section. Basic aspects of regeneration in different experimental biological systems as well as in the context of medical applications are dealt with in a special section that also contains information on technological advances for the elderly. Providing a primary source of high-quality papers covering all aspects of aging in humans and animals, ''Gerontology'' serves as an ideal information tool for all readers interested in the topic of aging from a broad perspective.
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