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1.
Biochem Biophys Res Commun ; 504(4): 916-920, 2018 10 12.
Article in English | MEDLINE | ID: mdl-30224059

ABSTRACT

Catabolism of the branched-chain amino acids (BCAAs: leucine, isoleucine, and valine) is regulated by the branched-chain α-ketoacid dehydrogenase (BCKDH) complex, which in turn is regulated by phosphorylation catalyzed by BCKDH kinase (BDK). Thiamine pyrophosphate (TPP) is required as a coenzyme for the E1 component of the BCKDH complex and can also bring about activation of the complex by inhibiting BDK. The present study shows that free Ca2+ in the physiological range greatly increases the sensitivity of BDK to inhibition by TPP (IC50 of 2.5 µM in the presence of 1 µM free Ca2+). This novel mechanism may be responsible for the stimulation of BCAA oxidation by conditions that increase mitochondrial free Ca2+ levels, e.g. in skeletal muscle during exercise.


Subject(s)
Calcium/metabolism , Protein Kinases/metabolism , Thiamine Pyrophosphate/metabolism , 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)/metabolism , Animals , Calcium/pharmacology , Male , Mitochondria, Muscle/metabolism , Muscle, Skeletal/metabolism , Phosphorylation , Protein Kinase Inhibitors/pharmacology , Rats, Sprague-Dawley , Serine/metabolism , Thiamine Pyrophosphate/pharmacology
2.
World J Surg Oncol ; 10: 99, 2012 May 31.
Article in English | MEDLINE | ID: mdl-22651848

ABSTRACT

BACKGROUND: Nitric oxide (NO) has been reported to be a key mediator in hepatocyte proliferation during liver regeneration. NO is the oxidative metabolite of L-arginine, and is produced by a family of enzymes, collective termed nitric oxide synthase (NOS). Thus, administration of L-arginine might enhance liver regeneration after a hepatectomy. Another amino acid, L-glutamine, which plays an important role in catabolic states and is a crucial factor in various cellular and organ functions, is widely known to enhance liver regeneration experimentally. Thus, the present study was undertaken to evaluate the effects of an L-arginine supplement on liver regeneration, and to compared this with supplementation with L-glutamine and L-alanine (the latter as a negative control), using a rat partial hepatectomy model. METHODS: Before and after a 70% hepatectomy, rats received one of three amino acid solutions (L-arginine, L-glutamine, or L-alanine). The effects on liver regeneration of the administered solutions were examined by assessment of restituted liver mass, staining for proliferating cell nuclear antigen (PCNA), and total RNA and DNA content 24 and 72 hours after the operation. RESULTS: At 72 hours after the hepatectomy, the restituted liver mass, the PCNA labeling index and the DNA quantity were all significantly higher in the L-arginine and L-glutamine groups than in the control. There were no significant differences in those parameters between the L-arginine and L-glutamine groups, nor were any significant differences found between the L-alanine group and the control. CONCLUSION: Oral supplements of L-arginine and L-glutamine enhanced liver regeneration after hepatectomy in rats, suggesting that an oral arginine supplement can clinically improve recovery after a major liver resection.


Subject(s)
Arginine/administration & dosage , Hepatectomy , Liver Diseases/surgery , Liver Regeneration/drug effects , Administration, Oral , Alanine/administration & dosage , Animals , DNA/genetics , Glutamine/administration & dosage , Immunoenzyme Techniques , Male , Polymerase Chain Reaction , Proliferating Cell Nuclear Antigen/metabolism , RNA/genetics , Rats , Rats, Wistar
3.
JPEN J Parenter Enteral Nutr ; 36(3): 337-43, 2012 May.
Article in English | MEDLINE | ID: mdl-22038205

ABSTRACT

It has been reported that branched-chain amino acid (BCAA) administration stimulates glucose uptake into muscles and whole body glucose oxidation in rats. The authors examined the effect of decreased plasma BCAA concentrations induced by clofibrate treatment on glucose tolerance in rats. Since clofibrate, a drug for hyperlipidemia (high serum triglyceride concentration), is a potent inhibitor of the branched-chain α-keto acid dehydrogenase kinase, clofibrate treatment (0.2 g/kg body weight) activated the hepatic branched-chain α-keto acid dehydrogenase complex, resulting in decreased plasma BCAA concentrations by 30% to 50% from the normal level. An intraperitoneal glucose tolerance test was conducted after clofibrate administration, and the results showed that peak plasma glucose concentration and the area under the curve of glucose concentration during the intraperitoneal glucose tolerance test were significantly higher in clofibrate-treated rats than in control rats. This impaired glucose tolerance in the clofibrate-treated rats was ameliorated by administration of BCAAs (0.45 g/kg body weight, leucine:isoleucine:valine = 2:1:1), which kept plasma BCAA concentrations at normal levels during the intraperitoneal glucose tolerance test. These results suggest that plasma BCAAs play an important role in maintaining normal glucose tolerance in rats.


Subject(s)
Amino Acids, Branched-Chain/blood , Clofibrate/pharmacology , Glucose Intolerance/etiology , Hypolipidemic Agents/pharmacology , Animals , Blood Glucose/analysis , Glucose Tolerance Test , Liver/enzymology , Male , Protein Kinase Inhibitors/pharmacology , Protein Kinases , Rats , Rats, Sprague-Dawley
4.
Biochem Biophys Res Commun ; 393(2): 303-7, 2010 Mar 05.
Article in English | MEDLINE | ID: mdl-20138840

ABSTRACT

Branched-chain alpha-keto acid dehydrogenase (BCKDH) kinase (BDK) is responsible for the regulation of BCKDH complex, which is the rate-limiting enzyme in the catabolism of branched-chain amino acids (BCAAs). In the present study, we investigated the expression and activity of hepatic BDK in spontaneous type 2 diabetes using hyperinsulinemic Zucker diabetic fatty rats aged 9weeks and hyperglycemic, but not hyperinsulinemic rats aged 18weeks. The abundance of hepatic BDK mRNA and total BDK protein did not correlate with changes in serum insulin concentrations. On the other hand, the amount of BDK bound to the complex and its kinase activity were correlated with alterations in serum insulin levels, suggesting that hyperinsulinemia upregulates hepatic BDK. The activity of BDK inversely corresponded with the BCKDH complex activity, which was suppressed in hyperinsulinemic rats. These results suggest that insulin regulates BCAA catabolism in type 2 diabetic rats by modulating the hepatic BDK activity.


Subject(s)
Amino Acids, Branched-Chain/metabolism , Diabetes Mellitus, Type 2/enzymology , Insulin/metabolism , Liver/enzymology , Protein Kinases/metabolism , Animals , Diabetes Mellitus, Type 2/blood , Disease Models, Animal , Insulin/blood , Male , Protein Kinases/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Rats, Zucker
5.
Yakugaku Zasshi ; 128(1): 129-33, 2008 Jan.
Article in Japanese | MEDLINE | ID: mdl-18176064

ABSTRACT

The antioxidative activity of phenylpropanoid compound extracts from nutmeg (Myristica fragragrans Houttuyn) seed was determined. The antioxidant activity was evaluated using the 1,1-diphenyl-2-picrylhydrazyl radical-scavenging method, superoxide disumutase assay, ferric thiocyanate assay, and radical-scavenging effect assay with electron-spin resonance. High antioxidant activity was found in monoterpenoid extracts including terpinene-4-ol (3), alpha-terpineol (4), and 4-allyl-2,6-dimethoxyphenol (12). Compound, 12 expressed particularly high antioxidant activity.


Subject(s)
Antioxidants/isolation & purification , Monoterpenes/isolation & purification , Myristica/chemistry , Seeds/chemistry , Antioxidants/pharmacology , Monoterpenes/pharmacology
6.
J Colloid Interface Sci ; 246(2): 288-95, 2002 Feb 15.
Article in English | MEDLINE | ID: mdl-16290413

ABSTRACT

Chitosan-derived polymer surfactants, sulfated N-acyl-chitosan (S-Cn-Chitosan), were synthesized and compared with commonly used low-molecular-weight surfactants, sodium dodecyl sulfate (SDS), dodecyltrimethyl ammonium chloride (DTAC), and octaethyleneglycol mono n-dodecyl ether (BL8SY), in their interaction with a lipid membrane using a spin probe method. A suspension of dipalmitoylphosphatidyl-choline (DPPC) spin-labeled strongly (10%) with a spin probe, 1-palmitoyl-2-(12-doxyl) stearoyl-phosphatidylcholine, was mixed with the surfactant solutions. The dissolution time of the DPPC membrane was estimated from the peak height change vs time, which was caused by the decrease in spin-exchange interaction. The times were 2, 4, and 70 s for BL8SY, SDS, and DTAC and 1.2 and 8.8 h for S-C10-Chitosan and S-C14-Chitosan, respectively, showing that the dissolution of the lipid membrane with polymer surfactants was far slower than that with low-molecular-weight surfactants. In addition, the time depended on the length of the alkyl chains of the polymer surfactants. Simulations of the ESR spectra of the DPPC-surfactant systems containing small amounts of surfactants were carried out in order to examine how the membrane structure was changed by the incorporation of surfactant molecules. By this analysis, it was revealed that the rigidity of the membrane was decreased by the addition of low-molecular-weight surfactants in the order of DTAC>SDS>BL8SY, inverse to the order of dissolution times. S-Cn-Chitosan, in contrast, increased the rigidity of the membrane, suggesting that polymer surfactants adhered to the lipid membrane and tightly enfolded the riposome anchoring their alkyl chains.


Subject(s)
1,2-Dipalmitoylphosphatidylcholine/metabolism , Chitosan/chemistry , Membranes, Artificial , Polymers/chemistry , Spin Labels , Surface-Active Agents/chemistry , 1,2-Dipalmitoylphosphatidylcholine/chemistry , Chitosan/metabolism , Polymers/metabolism , Surface-Active Agents/metabolism
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