Antioxidant effect of doxycycline decreases MMP activity and blood pressure in SHR

被引:40
作者
Antonio, Raquel C. [1 ]
Ceron, Carla S. [1 ]
Rizzi, Elen [1 ]
Coelho, Eduardo B. [2 ]
Tanus-Santos, Jose E. [1 ]
Gerlach, Raquel F. [3 ]
机构
[1] Fac Med Ribeirao Preto, Dept Pharmacol, Ribeirao Preto, SP, Brazil
[2] Fac Med Ribeirao Preto, Dept Internal Med, Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Dent Sch Ribeirao Preto, Dept Morphol & Physiol, BR-14040904 Ribeirao Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Hypertension; SHR; Doxycycline; Oxidative stress; MMPs; CIRCULATING MATRIX METALLOPROTEINASES; VASCULAR DYSFUNCTION; OXIDATIVE STRESS; HYPERTENSION; INHIBITION; MATRIX-METALLOPROTEINASE-9; TETRACYCLINES; INVOLVEMENT; APOPTOSIS; RECEPTOR;
D O I
10.1007/s11010-013-1848-7
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Increased matrix metalloproteinase (MMP) levels are involved in vascular remodeling of hypertension. In this study, we hypothesized that doxycycline (a MMP inhibitor) could exert antioxidant effects, reverse establish vascular remodeling, and lower blood pressure in spontaneously hypertensive rats (SHR). SHR and Wistar-Kyoto rats received either doxycycline at 30 mg/kg/day by gavage or vehicle. Systolic blood pressure (SBP) was assessed weekly by tail cuff. After 5 weeks of treatment, morphologic changes in the aortic wall were studied in hematoxylin/eosin sections. MMP activity and expression were determined by in situ zymography using DQ gelatin and immunofluorescence for MMP-2. Dihydroethidium was used to evaluate aortic reactive oxygen species (ROS) production by fluorescence microscopy. Doxycycline reduced SBP by 25 mmHg. However, the antihypertensive effects were not associated with significant reversal of hypertension-induced vascular hypertrophy. SHR showed increased aortic MMP-2 levels which co-localized with higher aortic MMP activity and ROS levels, and all those biochemical alterations associated with hypertension were blunted by treatment with doxycycline. These results show that MMP inhibition with doxycycline in SHR with established hypertension resulted in antioxidant effects, lower gelatinolytic activity, and antihypertensive effects which were not associated with reversal of hypertension-induced vascular remodeling.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 33 条
[1]
Different involvement of extracellular matrix components in small and large arteries during chronic NO synthase inhibition [J].
Bouvet, C ;
Gilbert, LA ;
Girardot, D ;
deBlois, D ;
Moreau, P .
HYPERTENSION, 2005, 45 (03) :432-437
[2]
Castier Y, 2009, ANTIOXID REDOX SIGN, V11, P1641, DOI 10.1089/ARS.2008.2393
[3]
Metalloproteinase inhibition ameliorates hypertension and prevents vascular dysfunction and remodeling in renovascular hypertensive rats [J].
Castro, Michele A. ;
Rizzi, Elen ;
Figueiredo-Lopes, Livia ;
Fernandes, Karla ;
Bendhack, Lusiane A. ;
Pitol, Dimitrius Leonardo ;
Gerlach, Raquel E. ;
Tanus-Santos, Jose E. .
ATHEROSCLEROSIS, 2008, 198 (02) :320-331
[4]
Castro MM, 2013, CURR DRUG TARGETS, V14, P335
[5]
Doxycycline ameliorates 2K-1C hypertension-induced vascular dysfunction in rats by attenuating oxidative stress and improving nitric oxide bioavailability [J].
Castro, Michele M. ;
Rizzi, Elen ;
Ceron, Carla S. ;
Guimaraes, Danielle A. ;
Rodrigues, Gerson J. ;
Bendhack, Lusiane M. ;
Gerlach, Raquel F. ;
Tanus-Santos, Jose Eduardo .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2012, 26 (03) :162-168
[6]
Matrix metalloproteinases: Targets for doxycycline to prevent the vascular alterations of hypertension [J].
Castro, Michele M. ;
Tanus-Santos, Jose E. ;
Gerlach, Raquel F. .
PHARMACOLOGICAL RESEARCH, 2011, 64 (06) :567-572
[7]
Antioxidant treatment reduces matrix metalloproteinase-2-induced vascular changes in renovascular hypertension [J].
Castro, Michele M. ;
Rizzi, Elen ;
Rodrigues, Gerson J. ;
Ceron, Carla S. ;
Bendhack, Lusiane M. ;
Gerlach, Raquel F. ;
Tanus-Santos, Jose E. .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 46 (09) :1298-1307
[8]
Pyrrolidine dithiocarbamate down-regulates vascular matrix metalloproteinases and ameliorates vascular dysfunction and remodelling in renovascular hypertension [J].
Cau, S. B. A. ;
Guimaraes, D. A. ;
Rizzi, E. ;
Ceron, C. S. ;
Souza, L. L. ;
Tirapelli, C. R. ;
Gerlach, R. F. ;
Tanus-Santos, J. E. .
BRITISH JOURNAL OF PHARMACOLOGY, 2011, 164 (02) :372-381
[9]
Spironolactone and hydrochlorothiazide exert antioxidant effects and reduce vascular matrix metalloproteinase-2 activity and expression in a model of renovascular hypertension [J].
Ceron, C. S. ;
Castro, M. M. ;
Rizzi, E. ;
Montenegro, M. F. ;
Fontana, V. ;
Salgado, M. C. O. ;
Gerlach, R. F. ;
Tanus-Santos, J. E. .
BRITISH JOURNAL OF PHARMACOLOGY, 2010, 160 (01) :77-87
[10]
Time course involvement of matrix metalloproteinases in the vascular alterations of renovascular hypertension [J].
Ceron, Carla S. ;
Rizzi, Elen ;
Guimaraes, Danielle A. ;
Martins-Oliveira, Alisson ;
Cau, Stefany B. ;
Ramos, Junia ;
Gerlach, Raquel F. ;
Tanus-Santos, Jose E. .
MATRIX BIOLOGY, 2012, 31 (04) :261-270