Hu Yangyang, Yang Ke, Zhang Weiyun, Xue Mengxiao, Li Tingting, Wang Shengchen, Cui Xiaoyan, Zhang Liyang, Hu Yun, Luo Xugang
Poultry Mineral Nutrition Laboratory, College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066004, China.
Animals (Basel). 2024 Mar 21;14(6):979. doi: 10.3390/ani14060979.
A prior investigation revealed that a lack of Zinc (Zn) could hinder intestinal cell proliferation in broiler chickens; however, the mechanisms responsible for this effect remain unclear. We aimed to investigate the possible mechanisms of dietary Zn deficiency in inhibiting the jejunal cell proliferation of broilers. For this study, a total of 112 chickens (21 days old) were randomly divided into two treatments (seven replicate cages per treatment, eight chickens per replicate cage): the control group (CON) and the Zn deficiency group. The duration of feeding was 21 d. Chickens in the control group were provided with a basal diet containing an extra addition of 40 mg Zn/kg in the form of Zn sulfate, whereas chickens in the Zn deficiency group were given the basal diet with no Zn supplementation. The results indicated that, in comparison to the CON, Zn deficiency increased ( < 0.05) the duodenal and jejunal crypt depth (CD) of broilers on d 28 and jejunal and ileal CD on d 35, and decreased ( < 0.05) the duodenal, jejunal, and ileal villus height/crypt depth (VH/CD) on d 28 and the jejunal VH, jejunal and ileal villus surface area, and VH/CD on d 35. Furthermore, Zn deficiency decreased ( < 0.0001) the number of proliferating cell nuclear antigen-positive cells and downregulated ( < 0.01) the mRNA or protein expression levels of phosphatidylinositol 3-kinase (PI3K), phosphorylated PI3K, phosphorylated serine-threonine kinase (AKT), phosphorylated mechanistic target of rapamycin (mTOR), G protein-coupled receptor 39 (GPR39), and extracellular-regulated protein kinase, but upregulated ( < 0.05) the mRNA or protein expression levels of P38 mitogen-activated protein kinase, c-jun N-terminal kinase (JNK) 1 and JNK2, and phosphorylated protein kinase C in the jejunum of the broilers on d 42. It was concluded that dietary Zn deficiency inhibited cell proliferation possibly via the GPR39-mediated suppression of the PI3K/AKT/mTOR signaling pathway in the jejunum of broilers.
先前的一项调查显示,锌(Zn)缺乏会阻碍肉鸡肠道细胞的增殖;然而,造成这种影响的机制仍不清楚。我们旨在研究日粮锌缺乏抑制肉鸡空肠细胞增殖的可能机制。在本研究中,总共112只鸡(21日龄)被随机分为两种处理组(每组7个重复笼,每个重复笼8只鸡):对照组(CON)和锌缺乏组。饲养期为21天。对照组的鸡被给予基础日粮,额外添加40 mg Zn/kg硫酸锌形式的锌,而锌缺乏组的鸡则被给予不添加锌的基础日粮。结果表明,与对照组相比,锌缺乏使28日龄肉鸡的十二指肠和空肠隐窝深度(CD)以及35日龄肉鸡的空肠和回肠CD增加(P<0.05),并使28日龄肉鸡的十二指肠、空肠和回肠绒毛高度/隐窝深度(VH/CD)以及35日龄肉鸡的空肠VH、空肠和回肠绒毛表面积以及VH/CD降低(P<0.05)。此外,锌缺乏使增殖细胞核抗原阳性细胞数量减少(P<0.0001),并使磷脂酰肌醇3激酶(PI3K)、磷酸化PI3K、磷酸化丝氨酸-苏氨酸激酶(AKT)、磷酸化雷帕霉素靶蛋白(mTOR)、G蛋白偶联受体39(GPR39)和细胞外调节蛋白激酶的mRNA或蛋白表达水平下调(P<0.01),但使42日龄肉鸡空肠中P38丝裂原活化蛋白激酶、c-jun氨基末端激酶(JNK)1和JNK2以及磷酸化蛋白激酶C的mRNA或蛋白表达水平上调(P<0.05)。得出的结论是,日粮锌缺乏可能通过GPR39介导的对肉鸡空肠中PI3K/AKT/mTOR信号通路的抑制来抑制细胞增殖。