ITH14001, a CGP37157-Nimodipine Hybrid Designed to Regulate Calcium Homeostasis and Oxidative Stress, Exerts Neuroprotection in Cerebral Ischemia

被引:22
作者
Buendia, Izaskun [1 ,2 ]
Tenti, Giammarco [3 ]
Michalska, Patrycja [1 ,2 ,4 ]
Mendez-Lopez, Iago [1 ,2 ,4 ]
Luengo, Enrique [1 ,2 ,4 ]
Satriani, Michele [1 ,2 ,3 ]
Padin-Nogueira, Fernando [1 ,2 ,4 ]
Lopez, Manuela G. [1 ,2 ,4 ]
Ramos, M. Teresa [3 ]
Garcia, Antonio G. [1 ,2 ,4 ]
Menendez, J. Carlos [3 ]
Leon, Rafael [1 ,2 ,4 ]
机构
[1] Univ Autonoma Madrid, Inst Teofilo Hernando, Madrid 28029, Spain
[2] Univ Autonoma Madrid, Dept Farmacol & Terapeut, Fac Med, Madrid 28029, Spain
[3] Univ Complutense, Fac Farm, Dept Quim Organ & Farmaceut, E-28040 Madrid, Spain
[4] Hosp Univ Princesa, Serv Farmacol Clin, Inst Invest Sanitaria, Madrid 28006, Spain
关键词
Calcium dyshomeostasis; cerebral ischemia; multitarget drugs; mitochondrial NCX; voltage dependent calcium channels; Nrf2; inducers; RAT HIPPOCAMPAL SLICES; MITOCHONDRIAL NA+/CA2+ EXCHANGER; CHROMAFFIN CELL-DEATH; PARKINSONS-DISEASE; ALZHEIMERS-DISEASE; CHANNEL ANTAGONISTS; PROTECTS NEURONS; DOUBLE-BLIND; GLUTAMATE; STROKE;
D O I
10.1021/acschemneuro.6b00181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During brain ischemia, oxygen and glucose deprivation induces calcium overload, extensive oxidative stress, neutoinflammation, and, finally, massive neuronal loss. In the search of a neuroprotective compound to mitigate this neuronal loss, we have designed and synthesized a new multitarget hybrid, (ITH14001) directed at the reduction of calcium overload by acting on two regulators of calcium homeostasis; the mitochondrial Na+/Ca2+-exchanger (mNCX). and L-type-voltage dependent calcium channels (VDCCs). This compound is a hybrid of CGP37157 (mNCX inhibitor) and nimodipine (L-type VDCCs blocker), and its pharmacological evaluation revealed a moderate ability to selectively inhibit both targets. These activities conferred concentration-dependent neuroprotection in two models of Ca2+ overload, such as toxicity induced by high K in the SH-SYSY cell line (60% protection at 30 mu M) and veratridine in hippocampal slices (26% protection at 10 mu M). It also showed neuroprotective effect against Oxidative stress, an activity related to its nitrogen radical scavenger effect and moderate induction of the Nif2-ARE pathway. Its Nrf2 induction capability was confirmed by the increase of the expression of the antioxidant and anti-inflammatory enzyme heme-oxygenase I (3-fold increase). In addition, the multitarget profile of ITH14001 led to anti-inflammatory properties, shown by the reduction of nitrites production induced by lipopolysaccharide in glial cultures. Finally, it showed protective effect in two acute models of cerebral ischemia in hippocampal slices, excitotoxicity induced by glutamate (31% protection at 10 mu M) and oxygen and glucose deprivation (76% protection at 10 mu M), reducing oxidative stress and iNOS deleterious induction. In, conclusion, our hybrid derivative showed improved neuroprotective properties When compared to its parent compounds CGP37157 and nimodipine.
引用
收藏
页码:67 / 81
页数:15
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