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Selenide Chitosan Sulfate Improved the Hepatocyte Activity, Growth Performance, and Anti-oxidation Capacity by Activating the Thioredoxin Reductase of Chickens In Vitro and In Vivo
Ist Teil von
Biological trace element research, 2022-08, Vol.200 (8), p.3798-3807
Ort / Verlag
New York: Springer US
Erscheinungsjahr
2022
Quelle
SpringerNature Journals
Beschreibungen/Notizen
Chicken hepatocytes were cultured in vitro and 240 specific pathogen-free (SPF) white leghorns chickens (7 days old) were obtained. The hepatocytes and chickens were randomly allocated to one of six treatment groups: control group; chitosan (COS) group; sodium selenite (Na
2
SeO
3
) group; selenide chitosan (COS-Se) group; chitosan sulfate (LS-COS) group; and selenide chitosan sulfate (LS-COS-Se) group. Our results showed that LS-COS-Se increased (
P
< 0.05) the activities of thioredoxin reductase (TXNRD), anti-superoxide anion radical (antiO
2
−
), and superoxide dismutase (SOD), the mRNA levels of thioredoxin reductase 1 (TXNRD1) and thioredoxin reductase 3 (TXNRD3), and the chicken body weight, but reduced (
P
< 0.05) the malondialdehyde (MDA) content and the lactate dehydrogenase (LDH) activity. Compared with COS and LS-COS, the LS-COS-Se treatment increased (
P
< 0.05) the activities of TXNRD, SOD, catalase (CAT), and the mRNA levels of TXNRD1 and TXNRD3, but reduced (
P
< 0.05) the MDA content in vitro, whereas, in vivo, it increased (
P
< 0.05) body weight on day 28; the activities of TXNRD, antiO
2
−
, and SOD; and the mRNA levels of TXNRD1 and TXNRD3. Compared with Na
2
SeO
3
and COS-Se, the LS-COS-Se treatment increased (
P
< 0.05) the TXNRD and SOD activities, the mRNA levels of TXNRD1 and TXNRD3 in vitro, increased (
P
< 0.05) the chicken body weight on day 28, and the TXNRD, antiO
2
−
, and SOD activities, but reduced (
P
< 0.05) the MDA content. These results indicated that LS-COS-Se was a useful antioxidant that improved hepatocyte activity, growth performance, and anti-oxidation capacity in hepatocytes (in vitro) and SPF chicken (in vivo) by activating the TXNRD system.