L-Citrulline Influences the Body Temperature, Heat Shock Response and Nitric Oxide Regeneration of Broilers Under Thermoneutral and Heat Stress Condition.
L-シトルリンは熱中立および熱ストレス条件下のブロイラーの体温、熱ショック応答、一酸化窒素再生に影響する (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
- 未確定
- 出版年
- 2021
- 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)
本研究は、急性熱ストレス(HS)下のブロイラーに対するL-シトルリン(L-Cit) supplementationの効果を検討した。Ross 308ブロイラー288羽を、熱中立(TNZ)またはHS(35℃、5時間)環境下で、対照食またはL-Cit添加食(1%)を与えた。HSは耳、直腸、深部体温を上昇させ、呼吸数を増加させたが、L-Citは平均深部体温を低下させた。抗酸化能では、HSでスーパーオキシドジスムターゼが増加し、L-Citはカタラーゼとグルタチオンペルオキシダーゼ活性を促進した。視床下部では、HSがHSP90を増加させたが、L-CitはHSF1とHSP60のmRNA発現を低下させ、TNZ下でHSF3を低下させた。血漿一酸化窒素(NO)はHSで増加したが、L-CitはNO産生を抑制し、総NOS活性を増加させた。アルギナーゼ活性はHSで増加したが、L-Citは抑制した。TNZ下では、L-CitはiNOS-COX2の発現と血清PGE2濃度を低下させた。以上より、L-Citは体温調節、抗酸化防御、熱ショック応答、NO再生に影響し、体温の中枢調節に関与する可能性が示唆された。
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抄録
Heat stress (HS) adversely affects several physiological responses in organisms, but the underlying molecular mechanisms involved are yet to be fully understood. L-Citrulline (L-Cit) is a nutraceutical amino acid that is gaining research interest for its role in body temperature regulation and nitric oxide synthesis. This study investigated whether dietary supplementation with L-Cit (1% of basal diet) could ameliorate the effects of acute HS on thermotolerance, redox balance, and inflammatory responses of broilers. Ross 308 broilers (288 chicks) were subjected to two environments; thermoneutral at 24°C (TNZ) or HS at 35°C for 5 h, and fed two diets; control or L-Cit. The results showed that HS increased the ear, rectal (RT), and core body (CBT) temperatures of broilers, along with higher respiratory rate. The RT and CBT readings were intermittently affected with time effect, whereas, L-Cit supplementation lowered the mean CBT than the control diet. Antioxidant assays showed that superoxide dismutase was increased during HS, while, catalase was promoted by L-Cit supplementation. In addition, L-Cit induced glutathione peroxidase activity compared to the control diet during HS. Hypothalamic heat shock protein (HSP)-90 was upregulated by HS, but L-Cit downregulated heat shock factor (HSF)-1, and HSP 60 mRNA expressions. HSF 3 mRNA expression was downregulated by L-Cit under TNZ condition. More so, HS increased the plasma nitric oxide (NO) concentration but lowered the total NO synthase (tNOS) activity. In contrast, L-Cit supplementation limited NO production but increased the tNOS activity. Arginase activity was increased in the control fed group during HS but L-Cit supplementation lowered this effect. The NOS-COX pathway was significantly affected under TNZ condition, since L-Cit supplementation downregulated the mRNA expression of iNOS-COX2 in the hypothalamus, and further reduced the serum PGE2 concentration. Together, these data indicates that L-Cit influenced the antioxidant defense, heat shock response and nitric oxide regeneration both under thermoneutral and HS conditions; and that L-Cit may be directly and/or indirectly involved in the central regulation of body temperature.
DOI 10.3389/fphys.2021.671691
PMID 34456742
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