Key Laboratory of Animal Physiology and Biochemistry, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China; MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.
Key Laboratory of Animal Physiology and Biochemistry, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China; MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.
Poult Sci. 2024 Jun;103(6):103734. doi: 10.1016/j.psj.2024.103734. Epub 2024 Apr 5.
Dietary supplementation with bioactive substances that can regulate lipid metabolism is an effective approach for reducing excessive fat deposition in chickens. Genistein (GEN) has the potential to alleviate fat deposition; however, the underlying mechanism of GEN's fat-reduction action in chickens remains unclear. Therefore, the present study aimed to explore the underlying mechanism of GEN on the reduction of fat deposition from a novel perspective: intercellular transmission of adipokine between adipocytes and hepatocytes. The findings showed that GEN enhanced the secretion of adiponectin (APN) in chicken adipocytes, and the enhancement effect of GEN was completely blocked when the cells were pretreated with inhibitors targeting estrogen receptor β (ERβ) or proliferator-activated receptor γ (PPARγ) signals, respectively. Furthermore, the results demonstrated that both co-treatment with GEN and APN or treatment with the medium supernatant (Med SUP) derived from chicken adipocytes treated with GEN significantly decreased the content of triglyceride and increased the protein levels of ERβ, Sirtuin 1 (SIRT1) and phosphor-AMP-activated protein kinase (p-AMPK) in chicken hepatocytes compared to the cells treated with GEN or APN alone. Moreover, the increase in the protein levels of SIRT1 and p-AMPK induced by GEN and APN co-treatment or Med SUP treatment were blocked in chicken hepatocytes pretreated with the inhibitor of ERβ signals. Importantly, the up-regulatory effect of GEN and APN co-treatment or Med SUP treatment on the protein level of p-AMPK was also blocked in chicken hepatocytes pretreated with a SIRT1 inhibitor; however, the increase in the protein level of SIRT1 induced by GEN and APN co-treatment or Med SUP treatment was not reversed when the hepatocytes were pretreated with an AMPK inhibitor. In conclusion, the present study demonstrated that GEN enhanced APN secretion by activating the ERβ-Erk-PPARγ signaling pathway in chicken adipocytes. Subsequently, adipocyte-derived APN synergized with GEN to activate the ERβ-mediated SIRT1-AMPK signaling pathway in chicken hepatocytes, ultimately reducing fat deposition. These findings provide substantial evidence from a novel perspective, supporting the potential use of GEN as a dietary supplement to prevent excessive fat deposition in poultry.
膳食补充具有调节脂代谢的生物活性物质是减少鸡体内脂肪过度沉积的有效方法。染料木黄酮(GEN)具有减轻脂肪沉积的潜力;然而,GEN 减少鸡脂肪沉积的作用机制尚不清楚。因此,本研究旨在从一个新的角度探讨 GEN 减少脂肪沉积的潜在机制:脂肪细胞和肝细胞之间的脂肪因子的细胞间传递。研究结果表明,GEN 增强了鸡脂肪细胞中脂联素(APN)的分泌,当细胞分别用雌激素受体β(ERβ)或过氧化物酶体增殖物激活受体γ(PPARγ)信号的抑制剂预处理时,GEN 的增强作用完全被阻断。此外,结果表明,与单独用 GEN 或 APN 处理的细胞相比,同时用 GEN 和 APN 处理或用 GEN 处理的鸡脂肪细胞的上清液(Med SUP)处理可显著降低鸡肝细胞中甘油三酯的含量,并增加 ERβ、Sirtuin 1(SIRT1)和磷酸化 AMP 激活蛋白激酶(p-AMPK)的蛋白水平。此外,在鸡肝细胞中用 ERβ 信号抑制剂预处理后,GEN 和 APN 共处理或 Med SUP 处理诱导的 SIRT1 和 p-AMPK 蛋白水平的增加被阻断。重要的是,在鸡肝细胞中用 SIRT1 抑制剂预处理后,GEN 和 APN 共处理或 Med SUP 处理对 p-AMPK 蛋白水平的上调作用也被阻断;然而,当用 AMPK 抑制剂预处理肝细胞时,GEN 和 APN 共处理或 Med SUP 处理诱导的 SIRT1 蛋白水平的增加并未逆转。总之,本研究表明,GEN 通过激活鸡脂肪细胞中的 ERβ-Erk-PPARγ 信号通路增强了 APN 的分泌。随后,脂肪细胞衍生的 APN 与 GEN 协同激活鸡肝细胞中的 ERβ 介导的 SIRT1-AMPK 信号通路,最终减少脂肪沉积。这些发现从一个新的角度提供了充分的证据,支持将 GEN 作为膳食补充剂用于预防家禽中脂肪过度沉积的潜力。