Related Experiment Video
Updated: May 10, 2025

04:23
The Creation of a Rat Model for Osteosarcopenia via Ovariectomy
Published on: February 21, 2025
180
Deciphering the relationship between sarcopenia and aging: A combined text mining and bioinformatics approach
Takahiro Kamihara1, Takuya Omura2, Atsuya Shimizu1
1Department of Cardiology, National Center for Geriatrics and Gerontology, Obu, Japan.
Geriatrics & Gerontology International
|April 21, 2025
Summary
Sarcopenia, an age-related muscle disease, is linked to oxidative stress regulation, specifically nicotinamide adenine dinucleotide phosphate oxidase pathways, rather than a complete failure of autophagy.
Area of Science:
- Gerontology
- Molecular Biology
- Bioinformatics
Background:
- Sarcopenia is an age-related muscle disease.
- Distinguishing sarcopenia from normal aging requires comprehensive analysis.
- Worldwide research on sarcopenia mechanisms is extensive.
Purpose of the Study:
- To differentiate gene-level changes in sarcopenia versus normal aging.
- To identify sarcopenia-specific molecular pathways using text mining and bioinformatics.
- To elucidate the underlying mechanisms of sarcopenia.
Main Methods:
- Text mining of PubMed articles on sarcopenia.
- Bioinformatics analysis of high-throughput sequencing data.
- Comparison of gene-level changes in sarcopenia and normal aging.
Main Results:
- Identified common pathways in sarcopenia and normal aging, including Interleukin-7.
- Phagosome-related pathways were not sarcopenia-specific.
- Genes in the nicotinamide adenine dinucleotide phosphate oxidase catalytic subunit family suggest oxidative stress involvement.
Conclusions:
- Sarcopenia may involve disrupted oxidative stress regulation, not a global autophagy failure.
- Nicotinamide adenine dinucleotide phosphate oxidase pathways are implicated in later stages of autophagy.
- Findings highlight oxidative stress as a key factor in sarcopenia pathogenesis.
Related Concept Videos
The Effect of Aging on Tissues
2.0K
Several body functions deteriorate with age. The external signs of aging are easily identifiable. For example, the skin becomes dry, less elastic, and thins out, forming wrinkles. The skin of the face begins to appear looser due to a decrease in the levels of elastic and collagen fibers in the connective tissue. Additionally, melanin production in the hair follicle decreases with age, resulting in gray hair. Moreover, the senses of sight and hearing decline, so glasses and hearing aids may...
2.0K
Bone Disorders
3.3K
Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
3.3K
Mitochondria
8.9K
Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
8.9K
Aging
24
Aging is a complex biological phenomenon influenced by various processes that affect cellular and systemic functions. Several prominent theories attempt to explain its mechanisms, highlighting cellular limitations, oxidative damage, and hormonal changes as central factors in aging.
Cellular Clock Theory
The cellular clock theory posits that the human lifespan is closely tied to the finite capacity of cells to divide, a phenomenon governed by telomeres, which are protective caps at the ends of...
Cellular Clock Theory
The cellular clock theory posits that the human lifespan is closely tied to the finite capacity of cells to divide, a phenomenon governed by telomeres, which are protective caps at the ends of...
24
PI3K/mTOR/AKT Signaling Pathway
3.3K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
3.3K
mTOR Signaling and Cancer Progression
3.6K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
The mTOR pathway or the...
3.6K

