2019
DOI: 10.1016/j.fsi.2019.04.296
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Effects of dietary supplementation with icariin on growth performance, antioxidant capacity and non-specific immunity of Chinese mitten crab (Eriocheir sinensis)

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Cited by 61 publications
(21 citation statements)
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“…ACP is a vital hydrolytic enzyme in phagocytic lysosomes [25,26], which participates in degradation of foreign proteins, carbohydrates, and lipids [27]. Our data revealed that the ACP activity was enhanced by exposure to TD 49 at various time intervals.…”
Section: Discussionmentioning
confidence: 71%
“…ACP is a vital hydrolytic enzyme in phagocytic lysosomes [25,26], which participates in degradation of foreign proteins, carbohydrates, and lipids [27]. Our data revealed that the ACP activity was enhanced by exposure to TD 49 at various time intervals.…”
Section: Discussionmentioning
confidence: 71%
“…Antioxidant status in fish, as determined by several antioxidant enzymes including CAT, SOD, GPx, and MDA have been considered as the first line of defensive biomarkers to protect cells and tissues from oxidative damage, caused by some free radicals such as superoxide anion (O 2-), hydrogen peroxide (H 2 O 2 ) and hydroxyl radical (OH) [80,81]. Glutathione peroxidase, GPx is an important antioxidant enzyme showing strong radical-scavenging capacity against free radicals and lipid peroxides [82].…”
Section: Plos Onementioning
confidence: 99%
“…A diet without ICA was used as the control (CON). The ingredients and proximal composition of the CON diet are the same as those reported previously (Zheng et al, 2019). The 32% fishmeal, 20% soybean meal, 13% peanut meal, 4.5% blood powder, and 2% rapeseed meal served as protein sources, and equal portions of fish oil and soybean oil (2.4%) were included as lipid sources.…”
Section: Diets Crab Management and Sample Collectionmentioning
confidence: 99%
“…Subsequently, a small piece of fresh ovary tissue was collected and fixed in Bouin's solution for ovarian histological analysis, and the remaining ovarian tissue and all the hepatopancreas tissue were quick-frozen in liquid nitrogen and stored at -80 • C for further analysis. Next, 0.5 mL of hemolymph was collected from each crab's second last pair of walking legs using a 1-mL sterile syringe, and mixed with pre-inhaled precooling crab anticoagulant solution at the ratio of 1:1 (Zheng et al, 2019), and immediately centrifuged at 9000 r/min and 4 • C for 20 min. The supernatant was collected and stored at -20 • C for later determination of VTG and gonadotropin releasing hormone (GnRH), FSH, and E 2 contents.…”
Section: Diets Crab Management and Sample Collectionmentioning
confidence: 99%