The cross-link breaker, N-phenacylthiazolium bromide prevents vascular advanced glycation end-product accumulation

被引:96
作者
Cooper, ME [1 ]
Thallas, V
Forbes, J
Scalbert, E
Sastra, S
Darby, I
Soulis, T
机构
[1] Univ Melbourne, Austin & Repatriat Med Ctr, Dept Med, W Heidelberg, Vic 3081, Australia
[2] IRIS, Courbevoie, France
[3] Royal Melbourne Inst Technol, Dept Human Biol, Bundoora, Vic, Australia
基金
英国医学研究理事会;
关键词
glycation; vascular; thiazolium; cross-link breaker;
D O I
10.1007/s001250051355
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. Advanced glycation is postulated to have a pivotal role in mediating diabetic vascular complications. The emergence of thiazolium compounds such as N-phenacylthiazolium bromide which cleave preformed advanced glycation end products (AGEs) has allowed us to explore the effects of these agents on the vascular AGE accumulation and hypertrophy associated with diabetes. Methods. Control and streptozotocin diabetic rats were selected at random for no treatment or treatment with. N-phenacylthiazolium bromide (10 mg/kg intraperitoneally) and followed for 3 weeks. In a separate study, intervention with N-phenacylthiazolium bromide was delayed until after 3 weeks of diabetes and then given for 3 weeks (total of 6 weeks). Results. Diabetes was associated with increased mesenteric vascular advanced glycation end products, as assessed by radioimmunoassay and immunohistochemistry. This increase in vascular AGE accumulation was prevented by N-phenacylthiazolium bromide treatment. Diabetes-associated mesenteric vascular hypertrophy was attenuated by treatment with N-phenacylthiazolium bromide only if given from the time of induction of diabetes. Conclusion/interpretation. Cross-link breakers seem to be effective in preventing or reversing accumulation of advanced glycation end-products in blood vessels and have the potential to play a part in the treatment of diabetic vascular complications.
引用
收藏
页码:660 / 664
页数:5
相关论文
共 15 条
[1]   LILLY LECTURE 1993 - GLYCATION AND DIABETIC COMPLICATIONS [J].
BROWNLEE, M .
DIABETES, 1994, 43 (06) :836-841
[2]   VALIDATION IN AWAKE RATS OF A TAIL-CUFF METHOD FOR MEASURING SYSTOLIC PRESSURE [J].
BUNAG, RD .
JOURNAL OF APPLIED PHYSIOLOGY, 1973, 34 (02) :279-282
[3]   DIABETES-ASSOCIATED MESENTERIC VASCULAR HYPERTROPHY IS ATTENUATED BY ANGIOTENSIN-CONVERTING ENZYME-INHIBITION [J].
COOPER, ME ;
RUMBLE, J ;
KOMERS, R ;
HECHENG, D ;
JANDELEIT, K ;
SHEUNGTO, C .
DIABETES, 1994, 43 (10) :1221-1228
[4]   AMINOGUANIDINE, A NOVEL INHIBITOR OF NITRIC-OXIDE FORMATION, PREVENTS DIABETIC VASCULAR DYSFUNCTION [J].
CORBETT, JA ;
TILTON, RG ;
CHANG, K ;
HASAN, KS ;
IDO, Y ;
WANG, JL ;
SWEETLAND, MA ;
LANCASTER, JR ;
WILLIAMSON, JR ;
MCDANIEL, ML .
DIABETES, 1992, 41 (04) :552-556
[5]   Renal fate of circulating advanced glycated end products (AGE): Evidence for reabsorption and catabolism of AGE-peptides by renal proximal tubular cells [J].
Gugliucci, A ;
Bendayan, M .
DIABETOLOGIA, 1996, 39 (02) :149-160
[6]   ADVANCED GLYCOSYLATION ENDPRODUCTS BLOCK THE ANTIPROLIFERATIVE EFFECT OF NITRIC-OXIDE - ROLE IN THE VASCULAR AND RENAL COMPLICATIONS OF DIABETES-MELLITUS [J].
HOGAN, M ;
CERAMI, A ;
BUCALA, R .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (03) :1110-1115
[7]   AMINOGUANIDINE TREATMENT INCREASES ELASTICITY AND DECREASES FLUID FILTRATION OF LARGE ARTERIES FROM DIABETIC RATS [J].
HUIJBERTS, MSP ;
WOLFFENBUTTEL, BHR ;
BOUDIER, HAJS ;
CRIJNS, FRL ;
KRUSEMAN, ACN ;
POITEVIN, P ;
LEVY, BI .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) :1407-1411
[8]   Angiotensin converting enzyme inhibition reduces the expression of transforming growth factor-β1 and type IV collagen in diabetic vasculopathy [J].
Rumble, JR ;
Gilbert, RE ;
Cox, A ;
Wu, L ;
Cooper, ME .
JOURNAL OF HYPERTENSION, 1998, 16 (11) :1603-1609
[9]   Vascular hypertrophy in experimental diabetes - Role of advanced glycation end products [J].
Rumble, JR ;
Cooper, ME ;
Soulis, T ;
Cox, A ;
Wu, L ;
Youssef, S ;
Jasik, M ;
Jerums, G ;
Gilbert, RE .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (05) :1016-1027
[10]  
Schwedler S., 1998, Journal of the American Society of Nephrology, V9, p641A