Antonopoulou Efthimia, Chouri Eleni, Feidantsis Konstantinos, Lazou Antigone, Chatzifotis Stavros
Laboratory of Animal Physiology, Department of Zoology, School of Biology, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Institute of Marine Biology, Biotechnology and Aquaculture, Hellenic Centre for Marine Research, 71003 Heraklion, Crete Greece.
J Biol Res (Thessalon). 2017 Dec 21;24:14. doi: 10.1186/s40709-017-0071-1. eCollection 2017 Dec.
Soybean is a common alternative protein source of plant origin in aquafeeds as it has a reasonably balanced amino acid profile and is widely available. This study aimed to investigate the influence of partial substitution of fish meal with soy meal on cytoprotective pathways and apoptosis in the digestive system of common dentex (), using the activation of Hsp70, p38 MAPK, Bcl-2 and caspase-3. The experimental approach involved feeding of common dentex with three isoprotein and isoenergetic diets that contained fish meal as a protein source (FM), partial replacement of fish meal by soy meal 25% (SM25) and 40% (SM40) for 3 months.
The SM40 diet induced Hsp70 activation only in the middle part of intestine. On the other hand, both SM25 and SM40 diets diminished the phosphorylation of p38 MAPK in the anterior and the middle part of intestine, whereas only SM25 induced p38 MAPK phosphorylation in the stomach. Moreover, a decrease in the levels of caspase-3 activity was observed in the middle and posterior intestine, as well as in the stomach after feeding with SM25 diets. Furthermore, Bcl-2 levels were increased by SM40 in the anterior and by SM25 in the middle part of intestine.
SM25 and SM40 diets elicited a tissue and soy concentration specific cellular and cell protective response in the different parts of the digestive tract in common dentex.
大豆是水产饲料中常见的植物源性替代蛋白质来源,因为其氨基酸组成较为平衡且广泛可得。本研究旨在通过检测热休克蛋白70(Hsp70)、p38丝裂原活化蛋白激酶(p38 MAPK)、Bcl-2和半胱天冬酶-3(caspase-3)的激活情况,研究用豆粕部分替代鱼粉对金头鲷消化系统细胞保护途径和细胞凋亡的影响。实验方法是用三种等蛋白、等能量的饲料喂养金头鲷,这三种饲料分别以鱼粉为蛋白质来源(FM)、用25%豆粕(SM25)和40%豆粕(SM40)部分替代鱼粉,持续喂养3个月。
SM40饲料仅在肠道中部诱导Hsp70激活。另一方面,SM25和SM40饲料均降低了肠道前部和中部p38 MAPK的磷酸化水平,而只有SM25诱导胃中p38 MAPK磷酸化。此外,喂食SM25饲料后,在肠道中部和后部以及胃中观察到caspase-3活性水平降低。此外,SM40使肠道前部的Bcl-2水平升高,SM25使肠道中部的Bcl-2水平升高。
SM25和SM40饲料在金头鲷消化道不同部位引发了组织和大豆浓度特异性的细胞及细胞保护反应。