A second site of vasopressin action on [1-14C]oleate metabolism in isolated rat hepatocytes: increased formation of 14CO2.
نویسندگان
چکیده
White-adipose-tissue lipogenesis showed a similar response to that of brown fat after glucose and insulin treatment in the three conditions, though the rates were severalfold lower in white adipose tissue. The differences in the basal lipogenesis in brown fat in the virgin, lactating and weaned states may be related to the plasma insulin concentration. Plasma insulin decreases during lactation (Robinson et al., 1978), but increases on weaning (Agius et af., 1979), and brown-adipose-tissue lipogenesis shows a similar pattern. The failure of glucose to elicit the same increase in lipogenesis during lactation as insulin suggests either that the insulin response to a glucose load may be decreased during lactation and weaning or that brown fat has a decreased sensitivity to insulin. The fate of the newly synthesized fatty acids in brown adipose tissue after a glucose load is not known. However, if the newly synthesized lipids are catabolized within the tissue, the decreased rate of lipogenesis during lactation may be important in the direction of substrates to the mammary gland by preventing the ultimate oxidation of lipogenic precursors in brown fat.
منابع مشابه
Impairment of effects of vasopressin on [1-14C]oleate metabolism in hepatocytes from obese (ob/ob) mice.
In hepatocytes from lean mice vasopressin decreased ketogenesis and increased 14CO2 production from [1-14C]oleate and glucose release; these effects were Ca2+-dependent. None of these effects of vasopressin were obtained with hepatocytes from obese (ob/ob) mice. Similarly, adrenaline did not increase 14CO2 production in these hepatocytes, but it stimulated glucose release. Possible reasons for ...
متن کاملEffects of mepacrine on the oxidation of [1-14C]oleate in isolated rat hepatocytes.
In isolated rat hepatocytes, mepacrine stimulated the conversion of [1-14C]oleate into 14CO2 and depressed the formation of acid-soluble products from [1-14C]oleate. The action of mepacrine on [1-14C]oleate oxidation was not affected by exogenously applied phospholipase A2 (from Crotalus adamanteus venom) or arachidonic acid. It is suggested that mepacrine may exert its metabolic effects in iso...
متن کاملMitochondrial glycerol-3-phosphate acyltransferase-1 directs the metabolic fate of exogenous fatty acids in hepatocytes.
Because excess triacylglycerol (TAG) in nonadipose tissues is closely associated with the development of insulin resistance, interest has increased in the metabolism of long-chain acyl-CoAs toward beta-oxidation or the synthesis and storage of TAG. To learn whether a mitochondrial isoform of glycerol-3-phosphate acyltransferase (mtGPAT1) competes with carnitine palmitoyltransferase I (CPT I) fo...
متن کاملMetabolic effects of bacitracin in isolated rat hepatocytes.
Bacitracin is a proteolytic inhibitor which interacts with the intracellular processing of insulin. Its effects on pyruvate, fatty acid and amino acid metabolism were examined in rat hepatocyte suspensions. Bacitracin (0.25-1.0 mM) increased the oxidation of [1-14C]pyruvate by 50-70% and presumably therefore increased the flux through pyruvate dehydrogenase. This was found both in the presence ...
متن کاملAccumulation of methylmalonic acid caused by vitamin B12-deficiency disrupts normal cellular metabolism in rat liver.
To clarify the relationship between intracellular concentrations of methylmalonic acid and metabolic and growth inhibition in vitamin B12-deficient rats, hepatic methylmalonic acid levels were assayed and inhibition of glucose and glutamic acid metabolism by methylmalonic acid was studied in isolated hepatocytes. Vitamin B12-deficient rats (14 weeks old) excreted more urinary methylmalonic acid...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Biochemical Society transactions
دوره 8 5 شماره
صفحات -
تاریخ انتشار 1980