Methionine metabolism via the transamination pathway in rat liver.
نویسندگان
چکیده
After incubation, the triacylglycerol-rich lipoproteins seen under the electron microscope appeared as partially degraded structures with atypical, discoid, flattened and lamellar forms. As shown in Table 1, heparin produced a significant increment in the hydrolysis of 3H-labelled esterified fatty acids and 14C-labelled acylglycerol glycerol from the 3Hand 14C-labelled triacylglycerol-rich lipoproteins in the medium. A significant proportion of the hydrolysed labelled lipids appeared incorporated into the tissue lipids at the end of incubation. Most of the 3H-labelled fatty acids appeared in their esterified form, whereas the I4C taken up by the tissue appeared distributed in unesterified fatty acids, esterified fatty acids and acylglycerol glycerol. The present results show that adipose tissue in uitro is able to utilize not only the fatty acids but also the glycerol moiety released by the action of lipoprotein lipase on the lipoprotein triacylglycerol. This effect is quantitatively small but effective, agreeing with the reported ability of adipose tissue to metabolize glycerol (Chaves & Herrera, 1978; Herrera & Ayanz, 1972). It may be significant in situations of hyperlipidaemia in the presence of augmented adipose-tissue lipoprotein lipase and glycerokinase activities, as in obesity (Rath et al., 1974; Treble & Mayer, 1963).
منابع مشابه
Identification of 3-methylthiopropionic acid as an intermediate in mammalian methionine metabolism in vitro.
The oxidative metabolism of methionine by a transaminative pathway was studied in rat and monkey tissue homogenates. Methionine was shown to undergo transamination followed by subsequent oxidation of its a-keto acid, a-keto-y-methiolbutyrate, to carbon dioxide in rat and monkey liver homogenates. Considerable transamination of methionine was observed in monkey kidney homogenates, but little of ...
متن کاملMethionine metabolism by rat muscle and other tissues. Occurrence of a new carnitine intermediate.
Perfused rat hindquarter preparations were shown to incorporate radioactivity from [U-14C]methionine into citrate-cycle intermediates, lactate, alanine, glutamate, glutamine and CO2. During perfusion, large amounts of methionine were also oxidized to methionine sulphoxide. The capacity for transamination of methionine or its oxo analogue, 4-methylthio-2-oxobutyrate, by muscle extracts was demon...
متن کاملInhibition of 5-Lipoxygenase inhibitor zileuton in high-fat diet-induced nonalcoholic fatty liver disease progression model
Objective(s): Arachidonic Acid/5-lipoxygenase (AA/5-LOX) pathway connects lipid metabolism and proinflammatory cytokine, which are both related to the development and progression of nonalcoholic fatty liver disease (NAFLD). Therefore, the present study was designed to investigate the role of AA/5-LOX pathway in progression of NAFLD, and the effect of zileuton, an inhibitor of 5-LOX, in this mod...
متن کاملIdentification of 2-keto-4-methylthiobutyrate as an intermediate compound in methionine synthesis from 5'-methylthioadenosine.
The synthesis of methionine from 5'-methylthioadenosine was examined in vitro using cell-free homogenates of rat liver. We had previously reported that methionine synthesized by this system contained carbons from the ribose moiety of 5'-methylthioadenosine (Backlund, P. S., Jr., and Smith, R. A. (1981) J. Biol. Chem. 256, 1533-1535). The present study examines some of the steps involved in this...
متن کاملMetabolic pathways of homoserine in the mammal.
The importance of homoserine in the metabolism of amino acids in a variety of living forms is now well established. This amino acid was found to be the common precursor of methionine and threonine in Neurospora crassa (1). Enzymes involved in the conversion of aspartic acid to threonine via homoserine have been studied in Escherichia coli (2-5) and in bakers’ yeast (6-S). The presence of homose...
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