Literature DB >> 3987975

Renal hypertrophy in experimental diabetes. Changes in pentose phosphate pathway activity.

K A Steer, M Sochor, P McLean.   

Abstract

An examination was made of the effect of different periods of experimental diabetes on the activity of the pentose phosphate pathway in rat kidney. A rapid increase in kidney weight, expressed both in absolute terms and in terms of body weight, occurred shortly after the induction of diabetes. The activity of the enzymes of the oxidative segment of the pentose phosphate pathway and the flux of glucose through the pathway were both increased during the first 7 days after induction of diabetes. Thereafter, enzyme activity returned toward control levels, but the increased functional activity of the pathway, as measured using specifically labeled glucose, persisted. In contrast, transketolase was significantly depressed at the time of most rapid kidney growth. A positive correlation was found between the rate of kidney growth and the change in activity of glucose-6-phosphate dehydrogenase and a negative correlation with changes in transketolase activity. The possible roles of the oxidative and nonoxidative segments of the pentose phosphate pathway in the kidney in early diabetes-induced renal hypertrophy are discussed.

Entities:  

Mesh:

Year:  1985        PMID: 3987975     DOI: 10.2337/diab.34.5.485

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  14 in total

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2.  Effect of in vitro glucose and diabetic hyperglycemia on mouse kidney protein synthesis: relevance to diabetic microangiopathy.

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3.  Concentration of phosphoribosyl pyrophosphate in the kidney during development and in experimental diabetic hypertrophy.

Authors:  S Kunjara; M Sochor; A Adeoya; P McLean; A L Greenbaum
Journal:  Biochem J       Date:  1986-03-15       Impact factor: 3.857

4.  Hepatic phosphoribosyl pyrophosphate concentration. Regulation by the oxidative pentose phosphate pathway and cellular energy status.

Authors:  S Kunjara; M Sochor; S A Ali; A L Greenbaum; P McLean
Journal:  Biochem J       Date:  1987-05-15       Impact factor: 3.857

5.  CRISPR-Mediated Single Nucleotide Polymorphism Modeling in Rats Reveals Insight Into Reduced Cardiovascular Risk Associated With Mediterranean G6PD Variant.

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6.  Serum metabolites are associated with all-cause mortality in chronic kidney disease.

Authors:  Jiun-Ruey Hu; Josef Coresh; Lesley A Inker; Andrew S Levey; Zihe Zheng; Casey M Rebholz; Adrienne Tin; Lawrence J Appel; Jingsha Chen; Mark J Sarnak; Morgan E Grams
Journal:  Kidney Int       Date:  2018-06-02       Impact factor: 10.612

7.  A role for glycosphingolipid accumulation in the renal hypertrophy of streptozotocin-induced diabetes mellitus.

Authors:  I Z Zador; G D Deshmukh; R Kunkel; K Johnson; N S Radin; J A Shayman
Journal:  J Clin Invest       Date:  1993-03       Impact factor: 14.808

8.  Selective impairment of hindquarters vasodilator responses to bradykinin in conscious Wistar rats with streptozotocin-induced diabetes mellitus.

Authors:  R J Kiff; S M Gardiner; A M Compton; T Bennett
Journal:  Br J Pharmacol       Date:  1991-06       Impact factor: 8.739

9.  Renal hypertrophy in experimental diabetes. The activity of the 'de novo' and salvage pathways of purine [corrected] synthesis.

Authors:  S Kunjara; S J Beardsley; A L Greenbaum
Journal:  Biochem J       Date:  1988-02-01       Impact factor: 3.857

10.  Renal hypertrophy in experimental diabetes. Effect of diabetes on the pathways of glucose metabolism: differential response in adult and immature rats.

Authors:  M Sochor; S Kunjara; A L Greenbaum; P McLean
Journal:  Biochem J       Date:  1986-03-15       Impact factor: 3.857

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