The effect of anagliptin on intimal hyperplasia of rat carotid artery after balloon injury.
The effect of anagliptin on intimal hyperplasia of rat carotid artery after balloon injury.
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阿格列汀对大鼠颈动脉球囊损伤后内膜增生的影响
DOI:
10.3892/mmr.2017.7667
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发表时间:
2017-12
影响因子:
3.4
通讯作者:
Chen C
中科院分区:
文献类型:
--
作者:
Li Q;Wu X;Liu Y;Zhang M;Bai X;Chen C
The present study evaluated the effect of anagliptin on intimal hyperplasia following carotid artery injury in Sprague-Dawley rats. Sprague-Dawley rats weighing 280–300 g were injured using a 2F Fogarty balloon embolectomy catheter. The rats were divided into injury-(saline) and anagliptin-(10 mg/kg/day) treated groups. vascular injuries were induced in the left carotid artery, followed by evaluation of neointima formation at 28 days. The right and left carotid arteries were harvested and evaluated with histological evaluation, and the plasma activity of glucagon-like peptide 1 receptor (GLP-1), stromal cell-derived factor (SDF)-1α, interleukin (IL)-6, IL-1β and tumor necrosis factor (TNF)-α were detected by ELISA analysis. Treatment with anagliptin decreased balloon injury-induced neointima formation, compared with the injury group (P<0.01). Body weight and food consumption did not alter following treatment with anagliptin. Anagliptin caused an increase in the serum active GLP-1 concentration, compared with the injury group. In addition, serum SDF-1α was significantly decreased by treatment with anagliptin (P<0.001). Anagliptin altered the serum activity of IL-6, IL-1β and TNF-α (P<0.01). The results of the present study demonstrated that anagliptin appeared to attenuate neointimal formation by inhibiting inflammatory cytokines and chemokines following balloon injury, and that treatment with a dipeptidyl peptidase 4 inhibitor may be useful for future preclinical studies and potentially for the inhibition of thrombosis formation following percutaneous coronary intervention.
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影响因子:
--
作者:
Paneghetti L;Ng YS
通讯作者:
Ng YS
影响因子:
24
作者:
McDonald RA;Halliday CA;Miller AM;Diver LA;Dakin RS;Montgomery J;McBride MW;Kennedy S;McClure JD;Robertson KE;Douglas G;Channon KM;Oldroyd KG;Baker AH
通讯作者:
Baker AH
DOI:
10.1161/circinterventions.116.003698
发表时间:
2016-08-01
影响因子:
5.6
作者:
Cassese, Salvatore;Hoppmann, Petra;Kastrati, Adnan
通讯作者:
Kastrati, Adnan
影响因子:
20.1
作者:
Abi-Younes, S;Sauty, A;Luster, AD
通讯作者:
Luster, AD
影响因子:
9.8
作者:
Hirano, Tsutomu;Yamashita, Satoko;Goto, Moritaka
通讯作者:
Goto, Moritaka