A novel therapeutic drug (copper nicotinic acid complex) for non-alcoholic fatty liver

被引:24
作者
Salama, Ragaa H. M. [1 ]
Nassar, Ahmed Y. A.
Nafady, Allam A. M.
Mohamed, Hesham H. T.
机构
[1] Assiut Univ, Fac Med, Dept Med Biochem, Assiut 71516, Egypt
[2] Assiut Univ, Fac Vet Med, Dept Pathol, Assiut 71516, Egypt
[3] Al Azhar Univ, Fac Pharm, Dept Biochem, Assiut Branch, Assiut, Egypt
关键词
animal model; copper complex; fatty liver; nutrition;
D O I
10.1111/j.1478-3231.2007.01460.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Fatty liver is the accumulation of fat in liver cells, which leads to disruption of the normal liver structure and function. Methods: A non-alcoholic fatty liver rat model received copper (Cu) (I)-nicotinate complex [CuCl(HNA) 2] for 4 weeks. Results: Clinical signs and histopathological examinations showed obvious improvements in rats that received Cu complex who were continuously on an (HCFF) diet than those returned to standard diet with Cu complex. The improvement was matched in total lipids in sera and hepatic tissue, with disappearance of fat droplets from liver sections. Furthermore, the gain in body weight and the corresponding decrease in liver weight, decreased liver transaminases and alkaline phosphatase were prominent. The oxidative stress markers such as nitric oxide, lipid peroxides, glutathione and superoxide dismutase were obviously changed to healthy normal levels. Conclusion: The Cu complex may serve as a novel chemical restoring agent in fatty degenerated liver cells and for renewal of their structure and functions. However, clinical trials are required for more evaluation of the Cu complex in humans.
引用
收藏
页码:454 / 464
页数:11
相关论文
共 35 条
[1]  
ANDY YS, 2002, REV GASTROENTEROL DI, V2, P11
[2]   Levels of serum vitamin A, alpha-tocopherol and malondialdehyde in patients with non-alcoholic steatohepatitis: relationship with histopathologic severity [J].
Bahcecioglu, IH ;
Yalniz, M ;
Ilhan, N ;
Ataseven, H ;
Ozercan, IH .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2005, 59 (03) :318-323
[3]   DOWN-REGULATION OF NADPH-DIAPHORASE (NITRIC-OXIDE SYNTHASE) MAY ACCOUNT FOR THE PHARMACOLOGICAL ACTIVITIES OF CU(II)(2)(3,5-DIISOPROPYLSALICYLATE)(4) [J].
BAQUIAL, JGL ;
SORENSON, JRJ .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1995, 60 (02) :133-148
[4]   Prevalence of and risk factors for nonalcoholic fatty liver disease: The Dionysos Nutrition and Liver Study [J].
Bedogni, G ;
Miglioli, L ;
Masutti, F ;
Tiribelli, C ;
Marchesini, G ;
Bellentani, S .
HEPATOLOGY, 2005, 42 (01) :44-52
[5]  
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[6]   Pharmacokinetic distribution of 67Cu(II)2[3,5-diisopropyl(carboxy-14C)salicylate]4 among murine tissues [J].
Blincoe, C ;
Chidambaram, M ;
Salari, H ;
Bond, KB ;
Evans, DT ;
Gray-Kaufman, RA ;
Griffey, HB ;
Tranby, SG ;
Garner-Johnson, B ;
Lee, T ;
Sorenson, JRJ .
CURRENT MEDICINAL CHEMISTRY, 2004, 11 (22) :3007-3015
[7]   Histological characteristics and prognosis in patients with fatty liver [J].
Dam-Larsen, S ;
Franzmann, MB ;
Christoffersen, P ;
Larsen, K ;
Becker, U ;
Bendtsen, F .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2005, 40 (04) :460-467
[8]   Management of dyslipidemia in patients with complicated metabolic syndrome [J].
Davidson, MH .
AMERICAN JOURNAL OF CARDIOLOGY, 2005, 96 (4A) :22E-25E
[9]   Steatohepatitis: A tale of two "hits"? [J].
Day, CP ;
James, OFW .
GASTROENTEROLOGY, 1998, 114 (04) :842-845
[10]   A new model of acute liver steatosis induced in rats by fasting followed by refeeding a high carbohydrate fat free diet. Biochemical and morphological analysis [J].
Delzenne, NM ;
Hernaux, NA ;
Taper, HS .
JOURNAL OF HEPATOLOGY, 1997, 26 (04) :880-885