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N-hexacosanol ameliorates streptozotocin-induced diabetic rat nephropathy.

Abstract
In this study we investigated the effects of N-hexacosanol on streptozotocin-induced rat diabetic nephropathy. Diabetes was induced in 8-week-old male Sprague-Dawley rats by administering an intraperitoneal injection of streptozotocin (50 mg/kg). The rats were divided into four groups and maintained for 8 weeks: control rats, diabetic rats without treatment with N-hexacosanol, and diabetic rats treated with N-hexacosanol (2 mg/kg and 8 mg/kg i.p. every day). Although N-hexacosanol failed to modify the diabetic status, increases in serum creatinine as well as in kidney weight were significantly reduced. The malonaldehyde and transforming growth factor beta-1 (TGF-beta1) concentrations as well as the protein kinase C (PKC) activities in the diabetic kidney were significantly higher than those of the control, which were decreased by treatment with N-hexacosanol. Histological examinations revealed that N-hexacosanol significantly ameliorated diabetic-induced tubulointerstitial pathological changes. Our data suggest that N-hexacosanol could prevent increases in the malonaldehyde and TGF-beta1 concentrations and PKC activities in the kidney, and ameliorate diabetic-induced nephropathy.
AuthorsMotoaki Saito, Yukako Kinoshita, Itaru Satoh, Chiko Shinbori, Tomoharu Kono, Takuya Hanada, Jiro Uemasu, Hiroto Suzuki, Masashi Yamada, Keisuke Satoh
JournalEuropean journal of pharmacology (Eur J Pharmacol) Vol. 544 Issue 1-3 Pg. 132-7 (Aug 21 2006) ISSN: 0014-2999 [Print] Netherlands
PMID16859672 (Publication Type: Journal Article)
Chemical References
  • Fatty Alcohols
  • Insulin
  • Transforming Growth Factor beta1
  • Malondialdehyde
  • Streptozocin
  • Creatinine
  • Protein Kinase C
  • 1-hexacosanol
Topics
  • Animals
  • Blood Urea Nitrogen
  • Creatinine (metabolism)
  • Diabetic Nephropathies (chemically induced, pathology)
  • Fatty Alcohols (pharmacology)
  • Insulin (metabolism)
  • Male
  • Malondialdehyde (metabolism)
  • Protein Kinase C (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Streptozocin (pharmacology)
  • Transforming Growth Factor beta1 (metabolism)

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