ZERO WORLD RESEARCHアミノ酸・有機酸の学術文献データベース

L-citrulline supplementation reverses the impaired airway relaxation in neonatal rats exposed to hyperoxia.

L-シトルリン補充は高酸素曝露を受けた新生児ラットの気道弛緩障害を回復させる (機械翻訳の邦題)

Respiratory research2012Sopi RB, Zaidi SI, Mladenov M, et al.
研究デザインその他の原著論文
対象動物

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研究デザイン
その他の原著論文
対象
動物
出版年
2012
出典
doi.org
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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)

高酸素曝露は一酸化窒素合成酵素(NOS)へのL-アルギニン供給を制限し、NO産生を減少させることで気道弛緩を障害する。本研究では、高酸素曝露ラット気管平滑筋の弛緩障害に対するL-シトルリン補充の効果を検討した。12日齢ラットを7日間高酸素または室内空気に曝露し、電気刺激による弛緩反応を測定した。高酸素曝露により弛緩反応は有意に低下したが、L-シトルリン補充(in vivoおよびin vitro)により回復した。また、NOS阻害による弛緩低下もL-シトルリンで回復したが、アルギニノコハク酸合成酵素またはリアーゼ阻害によりその効果は消失した。これらの結果から、気道にはL-シトルリン/L-アルギニン回路が存在し、基質制限条件下でL-シトルリンがL-アルギニン源として重要であり、補充が高酸素による気道弛緩障害を回復させることが示された。

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抄録

Background: Hyperoxia is shown to impair airway relaxation via limiting L-arginine bioavailability to nitric oxide synthase (NOS) and reducing NO production as a consequence. L-arginine can also be synthesized by L-citrulline recycling. The role of L-citrulline supplementation was investigated in the reversing of hyperoxia-induced impaired relaxation of rat tracheal smooth muscle (TSM).Methods: Electrical field stimulation (EFS, 2-20 V)-induced relaxation was measured under in vitro conditions in preconstricted tracheal preparations obtained from 12 day old rat pups exposed to room air or hyperoxia (>95% oxygen) for 7 days supplemented with L-citrulline or saline (in vitro or in vivo). The role of the L-citrulline/L-arginine cycle under basal conditions was studied by incubation of preparations in the presence of argininosuccinate synthase (ASS) inhibitor [α-methyl-D, L-aspartate, 1 mM] or argininosuccinate lyase inhibitor (ASL) succinate (1 mM) and/or NOS inhibitor [Nω-nitro-L-arginine methyl ester; 100 μM] with respect to the presence or absence of L-citrulline (2 mM).Results: Hyperoxia impaired the EFS-induced relaxation of TSM as compared to room air control (p < 0.001; 0.5 ± 0.1% at 2 V to 50.6 ± 5.7% at 20 V in hyperoxic group: 0.7 ± 0.2 at 2 V to 80.0 ± 5.6% at 20 V in room air group). Inhibition of ASS or ASL, and L-citrulline supplementation did not affect relaxation responses under basal conditions. However, inhibition of NOS significantly reduced relaxation responses (p < 0.001), which were restored to control level by L-citrulline. L-citrulline supplementation in vivo and in vitro also reversed the hyperoxia-impaired relaxation. The differences were significant (p <0.001; 0.8 ± 0.3% at 2 V to 47.1 ± 4.1% at 20 V without L-citrulline; 0.9 ± 0.3% at 2 V to 68.2 ± 4.8% at 20 V with L-citrulline). Inhibition of ASS or ASL prevented this effect of L-citrulline.Conclusion: The results indicate the presence of an L-citrulline/L-arginine cycle in the airways of rat pups. L-citrulline recycling does not play a major role under basal conditions in airways, but it has an important role under conditions of substrate limitations to NOS as a source of L-arginine, and L-citrulline supplementation reverses the impaired relaxation of airways under hyperoxic conditions.

MeSH

AnimalsAnimals, NewbornCitrullineDietary SupplementsHyperoxiaMuscle RelaxationMuscle, SmoothOrgan Culture TechniquesRandom AllocationRatsRats, Sprague-DawleyTrachea

DOI 10.1186/1465-9921-13-68

PMID 22870905

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