## Abstract The effect of the chronic administration of α‐MSH on the incorporation of tritiated tyrosine into noradrenalin and dopamine and of tritiated tryptophan into serotonin was studied in different regions of the rat brain. α‐MSH increased the incorporation of tritiated tryptophan into seroto
The effect of α-melanocyte stimulating hormone on gentamicin-induced acute nephrotoxicity in rats
✍ Scribed by Meltem Kolgazi; Serap Arbak; Inci Alican
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 253 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0260-437X
- DOI
- 10.1002/jat.1191
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The effect of α‐melanocyte stimulating hormone (α‐MSH) was investigated on gentamicin‐induced acute renal injury in rats. Sprague‐Dawley rats (200–250 g; n = 8–10) were treated with gentamicin sulphate (GEN; 80 mg kg^−1^) or saline intraperitoneally for 7 consecutive days. α‐MSH was administered at a dose of 25 µg rat^−1^ day^−1^ following GEN or saline injections. On day 8, all animals were decapitated. Trunk blood and 24 h urine were collected to measure the serum creatinine levels, blood urea nitrogen (BUN) levels and to calculate the creatinine clearance values. The kidneys were excised for histological evaluation and for the measurement of malondialdehyde (MDA) levels, glutathione (GSH) contents and myeloperoxidase (MPO) activity. Treatment with α‐MSH reduced the severity of the renal lesions microscopically, decreased MDA content and MPO activity and restored GSH in kidney samples. However, it did not restore the impaired renal function tests due to GEN challenge. In conclusion, α‐MSH treatment has a beneficial effect on GEN‐induced acute nephrotoxicity, as confirmed by histological evaluation and biochemical assays; but it does not improve GEN‐induced renal dysfunction. The mechanism of the protective effect could be attributed, at least in part, to decreased tissue leukocyte infiltration and thus, to decreased oxygen‐derived reactive metabolite production. Copyright © 2007 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
Peptidoglycan-polysaccharide fragments derived from cell walls of bacteria such as group A, but not group D, streptococci are arthritogenic in certain laboratory animals. For instance, systemic administration of these fragments into rats may induce a chronic polyarthritis which clinically, histologi
## Abstract Acute and subchronic administration of N‐methyl‐D‐aspartate antagonists to rats in the early postnatal period has been reported to produce widespread and selectively cortical neurotoxicity, respectively. To resolve this apparent discrepancy, we sought to clarify these data by determinin
The effects of glucose on CYP2E1 expression in rats with acute renal failure induced by uranyl nitrate (U-ARF) have been reported. CYP2E1 was significantly induced (2.3-fold) in rats with U-ARF compared with that in control rats. In contrast, CYP2E1 expression was significantly decreased in rats wit