Novel role of curcumin combined with bone marrow transplantation in reversing experimental diabetes: Effects on pancreatic islet regeneration, oxidative stress, and inflammatory cytokines

被引:73
作者
El-Azab, Mona F. [1 ]
Attia, Fadia M. [2 ]
El-Mowafy, Abdalla M. [3 ]
机构
[1] Suez Canal Univ, Fac Pharm, Dept Pharmacol & Toxicol, Ismailia 41522, Egypt
[2] Suez Canal Univ, Fac Med, Dept Clin Pathol, Ismailia 41522, Egypt
[3] Mansoura Univ, Dept Biochem, Fac Pharm, Mansoura 35112, Egypt
关键词
Curcumin; Bone marrow transplantation; Diabetes; Antioxidant; Inflammation; Islet regeneration; NF-KAPPA-B; ANTIOXIDANT STATUS; BETA-CELL; LIPID-PEROXIDATION; DIETARY CURCUMIN; IN-VITRO; GLUCOSE; MODELS; DEATH; RATS;
D O I
10.1016/j.ejphar.2011.02.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Therapeutic utility of bone marrow transplantation in diabetes is an attractive approach. However, the oxidative stress generated by hyperglycemia may hinder beta-cell regeneration. The present study was undertaken to investigate the therapeutic potential of curcumin, a dietary spice with antioxidant activity, bone marrow transplantation, and their combined effects in the reversal of experimental diabetes. Diabetes was induced in mice by multiple low doses of streptozotocin. After the onset of diabetes, mice were treated with curcumin (10 mM; 100 mu l/mouse, i.p., for 28 days) or received a single bone marrow transplantation (106 unfractionated bone morrow cells), or both. Parameters of diabetes, integrity of pancreatic islets, pancreatic oxidative stress markers, and serum pro-inflammatory cytokines, were evaluated. Treatment with either curcumin or bone marrow transplantation significantly reversed streptozotocin-induced hyperglycemia/glucose intolerance, hypoinsulinemia, and damage of pancreatic islets. Interestingly, combination of curcumin and bone marrow transplantation elicited the most profound alleviation of such streptozotocin-evoked anomalies; including islet regeneration/insulin secretion. On the other hand, curcumin, either alone or combined with bone marrow transplantation, blunted the pancreatic lipid-peroxidation, up-regulated activities of the antioxidant enzymes, and suppressed serum levels of TNF-alpha and IL-1 beta. Curcumin and single bone marrow transplantation proved their therapeutic potential in reversing diabetes when used in combination. Curcumin, via its antioxidant and anti-inflammatory effects, evidently enhanced the ability of bone marrow transplantation to regenerate functional pancreatic islets. Hence, the use of natural antioxidants combined with other therapeutic regimens to induce pancreatic regeneration is a promising strategy in the management of diabetes. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 48
页数:8
相关论文
共 54 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   Bioavailability of curcumin: Problems and promises [J].
Anand, Preetha ;
Kunnumakkara, Ajaikumar B. ;
Newman, Robert A. ;
Aggarwal, Bharat B. .
MOLECULAR PHARMACEUTICS, 2007, 4 (06) :807-818
[3]  
BABU PS, 1995, MOL CELL BIOCHEM, V152, P13
[4]   INSULIN-DEPENDENT DIABETES-MELLITUS AS AN AUTOIMMUNE-DISEASE [J].
BACH, JF .
ENDOCRINE REVIEWS, 1994, 15 (04) :516-542
[5]   Reversal of experimental diabetes by multiple bone marrow transplantation [J].
Banerjee, M ;
Kumar, A ;
Bhonde, RR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 328 (01) :318-325
[6]  
Banerjee Meenal, 2003, JOP, V4, P137
[7]   Making new beta cells from stem cells [J].
Colman, A .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2004, 15 (03) :337-345
[8]   Glucose may induce cell death through a free radical-mediated mechanism [J].
Donnini, D ;
Zambito, AM ;
Perrella, G ;
AmbesiImpiombato, FS ;
Curcio, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 219 (02) :412-417
[9]   Anti-angiogenic effect of resveratrol or curcumin in Ehrlich ascites carcinoma-bearing mice [J].
El-Azab, Mona ;
Hishe, Hailemichael ;
Moustafa, Yasser ;
El-Awady, El-Sayed .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2011, 652 (1-3) :7-14
[10]   Prominent Chemopreventive and Chemoenhancing Effects for Resveratrol: Unraveling Molecular Targets and the Role of C-Reactive Protein [J].
El-Mowafy, A. M. ;
El-Mesery, M. E. ;
Salem, H. A. ;
Al-Gayyar, M. M. ;
Darweish, M. M. .
CHEMOTHERAPY, 2010, 56 (01) :60-65