Supplementing L-Citrulline Can Extend Lifespan in C. elegans and Attenuate the Development of Aging-Related Impairments of Glucose Tolerance and Intestinal Barrier in Mice.
L-シトルリン補充はC. elegansの寿命を延長し、マウスの加齢に伴う耐糖能障害と腸管バリア障害の発症を軽減する (機械翻訳の邦題)
記録の確認項目
- 研究デザイン
- その他の原著論文
- 対象
- 動物
- 出版年
- 2023
- 出典
- doi.org
- 抄録の表示
- 表示あり
- 出版状態
- 有効な記録
- 状態確認日
- 2026/08/17
- 収集日
- 2026/08/03
- 鮮度
- 確認期限内
- 確認段階
- 自動処理
- 記録状態
- 公開
日本語要約(機械生成)
L-シトルリン(L-Cit)の寿命延長効果と加齢関連障害への影響を検討した。C. elegansではL-Cit処理により寿命が有意に延長した。12ヶ月齢のC57BL/6JマウスにL-Citを16または32週間投与したところ、対照群で見られた老化マーカーの増加と耐糖能障害がL-Cit投与群で軽減され、腸管バリア機能の保護と小腸のNO2-レベルの低下が認められた。一方、腸内細菌叢には顕著な差は見られなかった。薬理学的用量のL-Citは、C. elegansの寿命延長とマウスの加齢関連障害に対して有益な効果を持つ可能性が示唆された。
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抄録
L-Citrulline (L-Cit) is discussed to possess a protective effect on intestinal barrier dysfunction but also to diminish aging-associated degenerative processes. Here, the effects of L-Cit on lifespan were assessed in C. elegans, while the effects of L-Cit on aging-associated decline were determined in C57BL/6J mice. For lifespan analysis, C. elegans were treated with ±5 mM L-Cit. Twelve-month-old male C57BL/6J mice (n = 8-10/group) fed a standard chow diet received drinking water ± 2.5 g/kg/d L-Cit or 5 g/kg/d hydrolyzed soy protein (Iso-N-control) for 16 or 32 weeks. Additionally, 4-month-old C57BL/6J mice were treated accordingly for 8 weeks. Markers of senescence, glucose tolerance, intestinal barrier function, and intestinal microbiota composition were analyzed in mice. L-Cit treatment significantly extended the lifespan of C. elegans. The significant increase in markers of senescence and signs of impaired glucose tolerance found in 16- and 20-month-old control mice was attenuated in L-Cit-fed mice, which was associated with protection from intestinal barrier dysfunction and a decrease in NO2- levels in the small intestine, while no marked differences in intestinal microbiota composition were found when comparing age-matched groups. Our results suggest that pharmacological doses of L-Cit may have beneficial effects on lifespan in C. elegans and aging-associated decline in mice.
MeSH
DOI 10.3390/biom13111579
PMID 38002262
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