Nephroprotective potential of syringic acid in experimental diabetic nephropathy: Focus on oxidative stress and autophagy (Record no. 19742)
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control field | OSt |
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control field | 20230811165904.0 |
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fixed length control field | 230811b xxu||||| |||| 00| 0 eng d |
040 ## - CATALOGING SOURCE | |
Original cataloging agency | AIKTC-KRRC |
Transcribing agency | AIKTC-KRRC |
100 ## - MAIN ENTRY--PERSONAL NAME | |
9 (RLIN) | 21524 |
Author | Sherkhane, Bhoomika |
245 ## - TITLE STATEMENT | |
Title | Nephroprotective potential of syringic acid in experimental diabetic nephropathy: Focus on oxidative stress and autophagy |
250 ## - EDITION STATEMENT | |
Volume, Issue number | Vol.55(1), Jan-Feb |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Place of publication, distribution, etc. | Mumbai |
Name of publisher, distributor, etc. | Wolter Kluwer |
Year | 2022 |
300 ## - PHYSICAL DESCRIPTION | |
Pagination | 34-42p. |
520 ## - SUMMARY, ETC. | |
Summary, etc. | Diabetic nephropathy (DN) is a chronic hyperglycemic manifestation of microvascular damage in the kidneys. Widespread research in this area suggests the involvement of perturbed redox homeostasis and autophagy in renal cells phrase- promote the progression of DN. MATERIALS AND METHODS: Reframed sentences-The present study investigates the pharmacological effect of Syringic acid (SYA), in streptozotocin (STZ, 55 mg/kg, i.p) induced diabetic nephropathy model and in high glucose (30 mM) challenged rat renal epithelial cells (NRK 52E) cells with a focus on oxidative stress and autophagy mechanisms. RESULTS: Both in vivo and in vitro experimental data revealed elevated oxidative stress markers along with compromised levels of nuclear factor erythroid 2-related factor 2 (Nrf2), a pivotal cellular redox-regulated transcription factor in renal cells upon glycemic stress. Elevated blood glucose also reduced the autophagy process as indicated by low expression of light chain (LC) 3-IIB in diabetic kidney and in NRK 52E cells subjected to excess glucose. SYA (25 and 50 mg/kg, p.o.) administration for 4 weeks to diabetic rats, Reframed sentence-preserved the renal function as evidenced by reduced serum creatinine levels as well as improved urine creatinine and urea levles as compared to non treated diabetic animals. At the molecular level, SYA improved renal expression of Nrf2 and autophagy-related proteins (Atg5, Atg3, and Atg7) in diabetic rats. Similarly, SYA (10 and 20 μM) co-treatment in high glucose-treated NRK 52E cells displayed increased levels of Nrf2 and autophagy induction. CONCLUSION: Results from this study signify the renoprotective effect of SYA and highlight the modulation of oxidative stress and autophagy mechanisms to mitigate diabetic kidney disease. Keywords: Antioxidant enzymes, autophagy, diabetic nephropathy, oxidative stress, syringic acid |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
9 (RLIN) | 4774 |
Topical term or geographic name entry element | PHARMACOLOGY |
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9 (RLIN) | 21525 |
Co-Author | Yerra, Veera Ganesh |
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Place, publisher, and date of publication | Andheri - Mumbai Wolters Kluwer India Private Limited |
International Standard Serial Number | 0253-7613 |
Title | Indian Journal of Pharmacology |
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URL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204897/ |
Link text | Click here |
942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
Source of classification or shelving scheme | |
Koha item type | Articles Abstract Database |
Withdrawn status | Lost status | Source of classification or shelving scheme | Damaged status | Not for loan | Permanent Location | Current Location | Shelving location | Date acquired | Barcode | Date last seen | Price effective from | Koha item type |
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School of Pharmacy | School of Pharmacy | Archieval Section | 2023-08-11 | 2023-1153 | 2023-08-11 | 2023-08-11 | Articles Abstract Database |