Dietary myo-inositol deficiency decreased the growth performances and impaired intestinal physical barrier function partly relating to nrf2, jnk, e2f4 and mlck signaling in young grass carp (Ctenopharyngodon idella). Issue 67 (August 2017)

• Record Type: Journal Article
• Authors: Li, Shuang-An; Jiang, Wei-Dan; Feng, Lin; Liu, Yang; Wu, Pei; Jiang, Jun; Kuang, Sheng-Yao; Tang, Ling; Tang, Wu-Neng; Zhang, Yong-An; Tang, Xu; Shi, He-Qun; Zhou, Xiao-Qiu
• Is Part Of: Fish & shellfish immunology. Issue 67(2017)
• Page Start: 475
• Page End: 492
• Publication Date: 2017-08
• Subjects: Myo-inositol -- Grass carp (Ctenopharyngodon idella) -- Intestine -- Antioxidant -- Apoptosis -- Proliferation -- Tight junction; Fishes -- Immunology -- Periodicals; Shellfish -- Immunology -- Periodicals; Poissons -- Immunologie -- Périodiques; Crustacés -- Immunologie -- Périodiques; 571.9617
• DOI: 10.1016/j.fsi.2017.06.032
• Languages: English
• ISSNs: 1050-4648

Abstract

Abstract: In this study, we investigated the effects of dietary myo -inositol on the growth and intestinal physical barrier functions of young grass carp ( Ctenopharyngodon idella ). A total of 540 young grass carp (221.83 ± 0.84 g) were fed six diets containing graded levels of myo -inositol (27.0, 137.9, 286.8, 438.6, 587.7 and 737.3 mg/kg) for 10 weeks. After the growth trial, fish were challenged with Aeromonas hydrophila for 14 days. The results indicated that compared with optimal myo -inositol levels, myo -inositol deficiency (27.0 mg/kg diet):(1) decreased glutathione (GSH) contents and antioxidant enzymes activities, and down-regulated the mRNA levels of antioxidant enzymes [not glutathione-S-transferase ( gst ) p1 and gstp2 ] and NF-E2-related factor 2 ( nrf2 ), whereas up-regulated the reactive oxygen species (ROS), malondialdehyde (MDA) and protein carbonyl (PC) contents, and the mRNA levels of Kelch-like-ECH-associated protein 1 ( keap1 ) in three intestinal segments of young grass carp ( P < 0.05).(2) Up-regulated cysteinyl aspartic acid-protease ( caspase )- 2, -3, -7, -8, -9, apoptotic protease activating factor-1 ( apaf-1 ), Bcl2-associated X protein ( bax ), fas ligand ( fasl ), gen-activated protein kinase ( p38mapk ) and c-Jun N-terminal protein kinase ( jnk ) mRNA levels, whereas down-regulated B-cell lymphoma-2 ( bcl-2 ), inhibitor of apoptosis proteins ( iap ) and myeloid cell leukemia-1 ( mcl-1 ) mRNA levels in three intestinal segments of young grass carp ( P < 0.05).(3) Down-regulated mRNA levels of cell cycle proteins cyclin b, cyclin d, cyclin e and E2F transcription factor 4 ( e2f4 ) in three intestinal segments of young grass carp ( P < 0.05).(4) Down-regulated the mRNA levels of zonula occludens ( zo ) 1, zo-2, occludin, claudin-b, -c, -f, -3c, -7a, -7b as well as -11, and up-regulated the mRNA levels of claudin-12, -15a (not -15b ) and myosin light chain kinase ( mlck ) in three intestinal segments of young grass carp ( P < 0.05). All above data indicated that dietary myo -inositol deficiency could damage physical barrier function in three intestinal segments of fish. Finally, the myo -inositol requirements based on the percent weight gain (PWG), reactive oxygen species (ROS) contents in the proximal intestine (PI), relative mRNA levels of caspase-2 (PI), cyclin b (MI) as well as claudin-b (PI) were estimated to be 276.7, 304.1, 327.9, 416.7 and 313.2 mg/kg diet, respectively. Highlights: Compared with optimal myo -inositol supplementation: ● Myo -inositol deficiency caused intestine hypertrophy and hemorrhages of fish. ● Myo -inositol deficiency promoted cell apoptosis, decreased antioxidant capacity and cell proliferation in fish intestine. ● Myo -inositol deficiency destructed tight junctional complexes in the intestine of fish.