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Domest Anim Endocrinol ; 34(3): 269-77, 2008 Apr.
Article in English | MEDLINE | ID: mdl-17897805

ABSTRACT

In this study the hypothesis that irreversible glucose loss results in an 'uncoupling' of the somatotrophic axis (increasing plasma GH levels and decreasing plasma IGF-I) was tested. During periods of negative energy balance the somatotrophic axis respond by increasing plasma GH and decreasing plasma IGF-I levels. In turn, elevated GH repartitions nutrient by increasing lipolysis and protein synthesis, and decreases protein degradation. Irreversible glucose loss was induced using sub-cutaneous injections of phloridizin. Seven non-lactating cows were treated with 8g/day phloridizin (PHZ) and seven control animals (CTRL, 0g/day), while being restricted to a diet of 80% maintenance. PHZ treatment increased urinary glucose excretion (P<0.001), resulting in hypoglycemia (P<0.001). As a response to this glucose loss, the PHZ treated animals had elevated plasma NEFA (P<0.005) and BHBA (P<0.001) levels. Average plasma insulin concentrations were not altered with PHZ treatment (P=0.059). Plasma GH was not different between the two groups (P>0.1), whereas plasma IGF-I levels decreased significantly (P<0.001) with PHZ treatment. The decline in plasma IGF-I concentrations was mirrored by a decrease in the abundance of hepatic IGF-I mRNA (P=0.005), in addition the abundance of hepatic mRNA for both growth hormone receptors (GHR(tot) and GHR(1A)) was also decreased (P<0.05). Therefore, the irreversible glucose loss resulted in a partial 'uncoupling' of the somatotrophic axis, as no increase in plasma GH levels occurred although plasma IGF-I levels, hepatic IGF-I mRNA declined, and the abundance of liver GH receptor mRNA declined.


Subject(s)
Adaptation, Physiological/physiology , Cattle Diseases/metabolism , Glucose/metabolism , Malnutrition/veterinary , 3-Hydroxybutyric Acid/blood , Animals , Cattle , Fatty Acids, Nonesterified/blood , Female , Glycosuria/veterinary , Growth Hormone/blood , Hypoglycemia/veterinary , Insulin-Like Growth Factor I/analysis , Insulin-Like Growth Factor I/genetics , Lipolysis/physiology , Liver/chemistry , Malnutrition/metabolism , Phlorhizin/administration & dosage , Protein Biosynthesis/physiology , RNA, Messenger/analysis
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