Literature DB >> 23843825

Oxidative stress and raloxifene.

Gurkan Akgol1, Arif Gulkesen, Salih Ozgocmen.   

Abstract

Entities:  

Keywords:  Bone Metabolism; Raloxifene

Year:  2012        PMID: 23843825      PMCID: PMC3693630          DOI: 10.5812/ijem.5341

Source DB:  PubMed          Journal:  Int J Endocrinol Metab        ISSN: 1726-913X


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Dear Editor, We read “Effects of raloxifene on bone metabolism in hemodialysis patients with type 2 diabetes” by Saito et al. (1) with a great interest. This paper shows that raloxifene works in diabetic or non-diabetic hemodialysis patients to reduce bone loss. This was shown by means of significant decrease in NTx and a significant increase in SOS measurements in both treatment groups compared to the un-treated control arms. We would like to draw attention to the possible anti-oxidant role of raloxifene regarding beneficial effects on the bone turnover markers as well as bone mass. The targeted population in this study consisted hemodialysis patients with type 2 diabetes who under a great oxidative stress related to both renal failure and diabetes (2, 3). We have previously demonstrated that women with post-menopausal osteoporosis had lower erythrocyte catalase (CAT) enzyme activity and higher erythrocyte malondialdehyde (MDA) levels (4). Interestingly, in another study we showed that raloxifene treatment for 3 months significantly enhanced CAT enzyme activity and reduced the MDA levels in women with PMO (5). Similar anti-oxidant effects of raloxifene were confirmed by others (6). Although neither discussed nor studied by means of enzymatic parameters, we would like to attract Authors’ attention to the potent anti-oxidant effect of raloxifene particularly in this special study population. Significant decrease in N-terminal cross-linking telopeptide of type I collagen (NTx) as well as oxidative stress parameters has been achieved with the use of potent anti-oxidants (lycopene) in patients with PMO (7). We think the results of this present study should also be admissible regarding the anti-oxidant effects of raloxifene particularly in hemodialysis patients with type 2 diabetes who are under great oxidative stress.
  7 in total

1.  Effects of calcitonin, risedronate, and raloxifene on erythrocyte antioxidant enzyme activity, lipid peroxidation, and nitric oxide in postmenopausal osteoporosis.

Authors:  Salih Ozgocmen; Huseyin Kaya; Ersin Fadillioglu; Zumrut Yilmaz
Journal:  Arch Med Res       Date:  2006-12-04       Impact factor: 2.235

2.  Effects of raloxifene on serum malondialdehyde, erythrocyte superoxide dismutase, and erythrocyte glutathione peroxidase levels in healthy postmenopausal women.

Authors:  Hakan Kaya; Okan Ozkaya; Mekin Sezik; Evrim Arslanoglu; Arzu Yilmaztepe; Engin Ulukaya
Journal:  Maturitas       Date:  2005-03-14       Impact factor: 4.342

Review 3.  Oxidative stress and diabetic kidney disease.

Authors:  Robert C Stanton
Journal:  Curr Diab Rep       Date:  2011-08       Impact factor: 4.810

4.  Supplementation with the antioxidant lycopene significantly decreases oxidative stress parameters and the bone resorption marker N-telopeptide of type I collagen in postmenopausal women.

Authors:  E S Mackinnon; A V Rao; R G Josse; L G Rao
Journal:  Osteoporos Int       Date:  2010-06-15       Impact factor: 4.507

Review 5.  Oxidative stress and inflammation: Implications in uremia and hemodialysis.

Authors:  Carmelo Libetta; Vincenzo Sepe; Pasquale Esposito; Francesco Galli; Antonio Dal Canton
Journal:  Clin Biochem       Date:  2011-07-12       Impact factor: 3.281

6.  Role of antioxidant systems, lipid peroxidation, and nitric oxide in postmenopausal osteoporosis.

Authors:  Salih Ozgocmen; Huseyin Kaya; Ersin Fadillioglu; Rabia Aydogan; Zumrut Yilmaz
Journal:  Mol Cell Biochem       Date:  2006-07-14       Impact factor: 3.396

7.  Effects of raloxifene on bone metabolism in hemodialysis patients with type 2 diabetes.

Authors:  Osamu Saito; Takako Saito; Shinji Asakura; Tetsu Akimoto; Makoto Inoue; Yasuhiro Ando; Shigeaki Muto; Eiji Kusano
Journal:  Int J Endocrinol Metab       Date:  2012-04-20
  7 in total

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