Protective effects of valsartan on gentamicin induced tubular injury through down regulation of urinary N-acetyl-Y-D-glucosaminidase in rats (Record no. 15809)
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fixed length control field | a |
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control field | OSt |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20211229104328.0 |
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fixed length control field | 211229b xxu||||| |||| 00| 0 eng d |
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Original cataloging agency | AIKTC-KRRC |
Transcribing agency | AIKTC-KRRC |
100 ## - MAIN ENTRY--PERSONAL NAME | |
9 (RLIN) | 15185 |
Author | Li, Qi Xiong |
245 ## - TITLE STATEMENT | |
Title | Protective effects of valsartan on gentamicin induced tubular injury through down regulation of urinary N-acetyl-Y-D-glucosaminidase in rats |
250 ## - EDITION STATEMENT | |
Volume, Issue number | Vol.83(1), Jan-Feb |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Place of publication, distribution, etc. | Mumbai |
Name of publisher, distributor, etc. | Indian Journal of Pharmaceutical Science |
Year | 2021 |
300 ## - PHYSICAL DESCRIPTION | |
Pagination | 69-75p. |
520 ## - SUMMARY, ETC. | |
Summary, etc. | Urinary N-acetyl- β-D-glucosaminidase is a marker of early tubular damage. Therefore, the current study was to investigate effects and its underling mechanisms of valsartan on gentamicin induced renal tubular injury through urinary N-acetyl- β-D-glucosaminidase parameter variety in rats. Animals were divided into four groups consisting of 12 rats each. The study lasted for 10 d. Rats were treated in two batches on the 6 th and 11 th d of the experiment, with 6 rats in each group. Control group rats were administered with distilled water (10 ml/kg) daily via an intragastric gavage; gentamicin group rats were given gentamicin 100 mg/kg/d intraperitoneally; valsartan (10 mg/kg/d, intragastric gavage)+gentamicin group; valsartan (20 mg/kg/d, intragastric gavage)+gentamicin group. Rats treated with gentamicin showed significant elevation in the activity and expression of urinary N-acetyl- β-D-glucosaminidase as compared with the control group; the activities of superoxide dismutase, glutathione peroxidase and catalase were lower while malondialdehyde was higher in kidney tissues; urinary protein content was not changed; serum creatinine and blood urea nitrogen were increased. Moreover, pathological damage of the renal tubules was serious in gentamicin treated rats. Valsartan significantly inhibited activity and expression of urinary N-acetyl- β-D-glucosaminidase in a dose dependent manner; dramatically increased superoxide dismutase, glutathione peroxidase and catalase activities and markedly decreased malondialdehyde levels in kidney tissues; renal tubular structural damages were also effectively ameliorated by valsartan. These results show that changes of urinary N-acetyl- β-D- glucosaminidase levels can re flect the extent of renal tubular injury, that valsartan has protective role on gentamicin-induced renal tubular injury by down-regulation urinary N-acetyl- β-D-glucosaminidase, and its down-regulation urinary N-acetyl- β-D-glucosaminidase effect may be due to its antioxidant properties in kidney tissues. |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
9 (RLIN) | 4639 |
Topical term or geographic name entry element | PHARMACEUTICS |
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9 (RLIN) | 15186 |
Co-Author | Jiang, Xiao Ye |
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Place, publisher, and date of publication | New Delhi |
Title | Indian journal of pharmaceutical sciences |
856 ## - ELECTRONIC LOCATION AND ACCESS | |
URL | https://www.ijpsonline.com/articles/protective-effects-of-valsartan-on-gentamicin-induced-tubular-injury-through-down-regulation-of-urinary-nacetylbdglucosa.pdf |
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 | 2021-12-29 | 2021-2022626 | 2021-12-29 | 2021-12-29 | Articles Abstract Database |