Literature DB >> 34222086

The effect of methylethylpiridinol addition to the therapy on the level of pigment epithelium-derived factor and oxidative status in patients with diabetic nephropathy: randomized controlled open-label clinical study.

Sergey Sergeevich Popov1, Elena Igorevna Anufrieva1, Evgenii Dmitrievich Kryl'skii2, Konstantin Konstantinovich Shulgin2, Aleksey Nikolaevich Verevkin2, Tatyana Nikolaevna Popova2, Aleksander Nikolaevich Pashkov1.   

Abstract

PURPOSE: The diabetic nephropathy is associated with oxidative stress and increases in pigment epithelium-derived factor (PEDF) level in the patient's blood. For the first time, authors investigated the effect of methylethylpiridinol addition to the therapy on oxidative status and pigment epithelium-derived factor concentrations, and examined the relationship between these indicators and clinical markers of pathology development.
METHODS: Study design: open label randomized controlled trial study. Authors assessed the effect of methylethylpiridinol addition to the therapy vs basic treatment on antioxidant and NADPH-generating enzymes activity, glutathione's concentration and free radical-induced oxidation's intensity using a spectrophotometric method and iron-induced biochemiluminescence. The pigment epithelium-derived factor concentration in the serum was measured by enzyme-linked immunosorbent assay.
RESULTS: Patients receiving combination therapy with methylethylpiridinol showed a more substantial increase in activity of glutathione peroxidase (Δ = 0.04 ± 0.11, p = 0.002), glutathione transferase (Δ = 0.12 ± 0.08, p < 0.001) and the concentration of reduced glutathione (Δ = 0.30 ± 0.17, p = 0.039). In addition, there was a significant decrease in PEDF level (Δ = -6.4 ± 5.4, p = 0.004). Correlation analysis showed a negative link between Δ postprandial glucose and Δ NADP-isocitrate dehydrogenase (-0.39, p = 0.033), Δ reduced glutathione and Δ postprandial glucose (-0.372, p = 0.043), Δ glutathione transferase and Δ PEDF (-0.37, p = 0.044).
CONCLUSIONS: The methylethylpiridinol addition to the therapy had a more potent stimulating effect on the patients' oxidative status in comparison with standard treatment, and reliably decreased pigment epithelium-derived factor level in patients' serum. The observed differences seem to be associated with the antioxidant activity of methylethylpiridinol which contributing to the mitigation of oxidative stress reducing at diabetes mellitus. © Springer Nature Switzerland AG 2021.

Entities:  

Keywords:  Antioxidant system; Diabetic nephropathy; Methylethylpiridinol; Oxidative stress; Pigment epithelium-derived factor

Year:  2021        PMID: 34222086      PMCID: PMC8212231          DOI: 10.1007/s40200-021-00802-6

Source DB:  PubMed          Journal:  J Diabetes Metab Disord        ISSN: 2251-6581


  27 in total

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3.  Diabetes causes inhibition of glucose-6-phosphate dehydrogenase via activation of PKA, which contributes to oxidative stress in rat kidney cortex.

Authors:  Yizhen Xu; Brent W Osborne; Robert C Stanton
Journal:  Am J Physiol Renal Physiol       Date:  2005-06-14

4.  Pigment epithelium-derived factor (PEDF) blocks angiotensin II signaling in endothelial cells via suppression of NADPH oxidase: a novel anti-oxidative mechanism of PEDF.

Authors:  Sho-Ichi Yamagishi; Kazuo Nakamura; Seiji Ueda; Seiya Kato; Tsutomu Imaizumi
Journal:  Cell Tissue Res       Date:  2005-04-22       Impact factor: 5.249

5.  Electrochemical detection of glutathione S-transferase: an important enzyme in the cell protective mechanism against oxidative stress.

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6.  [Investigation of Free Radical Processes in Substrates and Biological Samples by Means of induced Chemiluminescence].

Authors:  I M Piskarev; S V Trofimova; O E Burkhina; I P Ivanova
Journal:  Biofizika       Date:  2015 May-Jun

7.  Genetic Regulation of Pigment Epithelium-Derived Factor (PEDF): An Exome-Chip Association Analysis in Chinese Subjects With Type 2 Diabetes.

Authors:  Chloe Y Y Cheung; Chi-Ho Lee; Clara S Tang; Aimin Xu; Ka-Wing Au; Carol H Y Fong; Kelvin K K Ng; Kelvin H M Kwok; Wing-Sun Chow; Yu-Cho Woo; Michele M A Yuen; JoJo Hai; Kathryn C B Tan; Tai-Hing Lam; Hung-Fat Tse; Pak-Chung Sham; Karen S L Lam
Journal:  Diabetes       Date:  2018-10-10       Impact factor: 9.461

8.  Protective Role of PEDF-Derived Synthetic Peptide Against Experimental Diabetic Nephropathy.

Authors:  Y Ishibashi; T Matsui; J Taira; Y Higashimoto; S Yamagishi
Journal:  Horm Metab Res       Date:  2016-05-23       Impact factor: 2.936

9.  Glutathione homeostasis and functions: potential targets for medical interventions.

Authors:  Volodymyr I Lushchak
Journal:  J Amino Acids       Date:  2012-02-28

Review 10.  Oxidative Stress in Diabetic Nephropathy with Early Chronic Kidney Disease.

Authors:  Alejandra Guillermina Miranda-Díaz; Leonardo Pazarín-Villaseñor; Francisco Gerardo Yanowsky-Escatell; Jorge Andrade-Sierra
Journal:  J Diabetes Res       Date:  2016-07-20       Impact factor: 4.011

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1.  Clinical Application of the Classical Theory of Traditional Chinese Medicine in Diabetic Nephropathy.

Authors:  Jintong Pan; Huihui Li; Junhua Shi
Journal:  Comput Math Methods Med       Date:  2022-04-20       Impact factor: 2.809

  1 in total

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