It was previously found that pertussis toxin (PTX) pretreatment inhibits the activation of extracellular signal-regulated kinases ERK1 (p44 mapk ) and ERK2 (p42 mapk ) in hepatocytes in response to either agonists that bind to heptahelical receptors or epidermal growth factor (EGF), suggesting a rol
Hormonal control of gluconeogenesis in rainbow trout hepatocytes: Regulatory role of pyruvate kinase
β Scribed by Petersen, T. D. P. ;Hochachka, P. W. ;Suarez, R. K.
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 731 KB
- Volume
- 243
- Category
- Article
- ISSN
- 0022-104X
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β¦ Synopsis
Gluconeogenesis from lactate in hepatocytes from rainbow trout is activated by glucagon and inhibited by insulin in a dose-dependent fashion. The maximal responses to both hormones occur within their probable physiological concentration ranges. Gluconeogenic activation by glucagon is accompanied by a profound inhibition of pyruvate kinase activity. This is reflected in increases in both the So.5 and nH for phosphoenolpyruvate and increased sensitivity to inhibition by MgATP compared to the enzyme isolated from cells not treated with hormone (control). Gluconeogenic inhibition by insulin is accompanied by activation of pyruvate kinase activity. This is observed as decreases in both the S0.5 and nH for phosphoenolpyruvate and a decreased sensitivity to inhibition by MgATP compared to enzyme isolated from control cells. These results indicate that insulin and glucagon are involved in the regulation of hepatic gluconeogenesis in trout and that their effects are mediated, at least partly, through the control of pyruvate kinase activity.
MATERIALS AND METHODS
Animals
Rainbow trout (Salmo gairdneri, Richardson) of both sexes (200-400 gm) were ob- tained from a local trout farm and kept in dechlorinated and aerated running freshwater at 10-15Β°C. The fish were maintained on Address reprint requests t o R.K. Suarez.
π SIMILAR VOLUMES
The role of diacylglycerol (DAG) in hormonal induction of S phase was investigated in primary cultures of rat hepatocytes. In this model, several agonists that bind to G protein-coupled receptors act as comitogens when added to the cells soon after plating (i.e., in Go/early Gl phase), while the cel