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Gen Comp Endocrinol ; 261: 89-96, 2018 05 15.
Artículo en Inglés | MEDLINE | ID: mdl-29407384

RESUMEN

A study was carried out to assess the regulation of compensatory growth under different restriction feeding regimes in Labeo rohita juveniles by the interaction of various feed intake and growth regulating genes. A 60 day feeding trial was conducted with five treatment groups, Control (3% body weight, bw), T1 (alternate days), T2 (0.5% bw), T3 (1% bw) and T4 (2% bw) and feeding was done for first 30 days of the trial. For next 30 days, all the treatment groups were fed at a rate of 3% bw as in the control group. There was significant (p < 0.05) difference in the weight gain among the treatment groups with lowest FCR and highest PER was found in T2 group. Ghrelin gene mRNA levels were upregulated during first 30th days of the trial with highest expression levels in the T2 group. The expression levels of leptin gene mRNA were found significantly different (p < 0.05) among the treatments, which was down-regulated during initial 30 days and upregulated as the experiment progress towards 60th day. The IGF-1 mRNA expression levels were upregulated more in liver compared to the muscle tissue. The results of the study suggest that increased ghrelin levels and decreased leptin levels lead to hyperphagia during the onset of refeeding, which further triggers the compensatory growth in L. rohita. The present study describes the molecular mechanism behind the compensatory growth following a different feed restriction regime in L. rohita which is regulated due to the interaction of different energy homeostasis and growth regulating genes.


Asunto(s)
Cyprinidae/crecimiento & desarrollo , Cyprinidae/fisiología , Conducta Alimentaria , Animales , Peso Corporal , Regulación de la Expresión Génica , Ghrelina/genética , Ghrelina/metabolismo , Factor I del Crecimiento Similar a la Insulina/genética , Factor I del Crecimiento Similar a la Insulina/metabolismo , Leptina/genética , Leptina/metabolismo , Hígado/metabolismo , ARN Mensajero/genética , ARN Mensajero/metabolismo , Receptores de Ghrelina/genética , Receptores de Ghrelina/metabolismo
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