Biological Sciences Department, Center for Coastal Marine Sciences, California Polytechnic State University, San Luis Obispo, CA 93407, USA.
Lynker Technology, 202 Church St SE #536, Leesburg, VA 20175, USA; Under Contract to Environmental and Fisheries Sciences Division, Northwest Fisheries Science Center, National Marine Fisheries Service, National Oceanic and Atmospheric Administration, Seattle, WA 98112, USA.
Comp Biochem Physiol A Mol Integr Physiol. 2023 Aug;282:111444. doi: 10.1016/j.cbpa.2023.111444. Epub 2023 May 16.
Fish adjust rates of somatic growth in the face of changing food consumption. As in other vertebrates, growth in fish is regulated by the growth hormone (Gh)/insulin-like growth factor-1 (Igf1) endocrine axis, and changes in food intake impact growth via alterations to Gh/Igf1 signaling. Understanding the time course by which the Gh/Igf1 axis responds to food consumption is crucial to predict how rapidly changes in food abundance might lead to altered growth dynamics. Here, we looked at the response times of plasma Igf1 and liver Igf1 signaling-associated gene expression to refeeding after food deprivation in juvenile gopher rockfish (Sebastes carnatus), one of several species of northern Pacific Ocean Sebastes rockfishes targeted by fisheries or utilized for aquaculture. Gopher rockfish were fasted for 30 d, after which a subset was fed to satiation for 2 h, while other rockfish continued to be fasted. Refed fish exhibited higher hepatosomatic index (HSI) values and increased Igf1 after food consumption. Gene transcripts for Gh receptor 1 (ghr1), but not ghr2, increased in the liver 2-4 d after eating. Transcripts encoding igf1also increased in the liver of refed fish by 4 d after feeding, only to return to levels similar as continually fasted rockfish by 9 d after feeding. Liver mRNA abundances for Igf binding protein (Igfbp) genes igfbp1a, igfbp1b, and igfbp3a declined within 2 d of feeding. These findings provide evidence that circulating Igf1 in rockfish reflects a fish's feeding experience within the previous few days, and suggest that feeding-induced increases in Igf1 are being mediated in part by altered liver sensitivity to Gh due to upregulated Gh receptor 1 expression.
鱼类会根据食物消耗的变化来调整体生长速度。与其他脊椎动物一样,鱼类的生长受生长激素(Gh)/胰岛素样生长因子 1(Igf1)内分泌轴的调节,而食物摄入的变化会通过改变 Gh/Igf1 信号来影响生长。了解 Gh/Igf1 轴对食物摄入的反应时间对于预测食物丰度的变化如何迅速导致生长动态的改变至关重要。在这里,我们研究了在经历食物剥夺后重新进食时,血浆 Igf1 和肝脏 Igf1 信号相关基因表达对再进食的反应时间,这是北太平洋几种 Sebastes 石斑鱼(Sebastes carnatus)之一,这些石斑鱼是渔业的目标或用于水产养殖。幼鱼石斑鱼被禁食 30 天,然后一部分鱼被喂食至饱食 2 小时,而其他鱼继续禁食。再进食的鱼表现出更高的肝体比(HSI)值和更高的 Igf1 水平。Gh 受体 1(ghr1)的基因转录物,但不是 ghr2,在进食后 2-4 天在肝脏中增加。进食后 4 天,再进食鱼的肝脏中编码 Igf1 的转录物也增加,但到喂食后 9 天,其水平又恢复到与持续禁食的石斑鱼相似的水平。肝脏中 Igf 结合蛋白(Igfbp)基因 igfbp1a、igfbp1b 和 igfbp3a 的 mRNA 丰度在进食后 2 天内下降。这些发现表明,石斑鱼循环中的 Igf1 反映了鱼类在过去几天的摄食经历,并表明摄食诱导的 Igf1 增加部分是由于 Gh 受体 1 表达上调导致肝脏对 Gh 的敏感性增加而介导的。