Nicardipine: A Hypotensive Dihydropyridine-Type Calcium Antagonist with a Peculiar Cerebrovascular Profile

被引:19
作者
Amenta, Francesco [1 ]
Tomassoni, Daniele [1 ]
Traini, Enea [1 ]
Mignini, Fiorenzo [1 ]
Veglio, Franco [2 ]
机构
[1] Univ Camerino, Dipartimento Med Sperimentale & Sanita Pubbl, Ctr Rech Clin, I-62032 Camerino, MC, Italy
[2] Univ Turin, Ctr Ipertens, Dipartimento Med & Oncol Sperimentale, Turin, Italy
关键词
nicardipine; hypertension; vascular dementia; subarachnoid haemorrhage; stroke;
D O I
10.1080/10641960802580190
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Control of blood pressure protects against the development of cerebrovascular lesions, stroke, and vascular dementia (VaD). Cerebrovascular disease is increasingly recognized as a cause of cognitive impairment and dementia primarily in the elderly. Nicardipine is a dihydropyridine-type calcium channel blocker (CCB) with a peculiar cerebrovascular profile developed approximately 30 years ago. This study has reviewed the main controlled clinical studies investigating the use of nicardipine in pathologies associated with cerebrovascular injury, such as subarachnoid haemorrhage (SAH), acute stroke, and VaD. SAH is a main cerebrovascular indication of CCBs. In this indication, CCBs prevent vasospasm and improve clinical outcomes. Nimodipine represents the CCB more investigated in this indication. Former studies did not demonstrate a clear advantage of nicardipine versus nimodipine in SAH. A more recent approach using implants of nicardipine prolonged-release showed a decreased incidence of vasospasm, delayed ischemic deficits, and improved clinical outcome after severe SAH. Controlled trials have shown the effectiveness of the drug in preventing stroke. Increasing evidence suggests some benefit of some CCBs in VaD or mixed degenerative and vascular dementia. In this setting, nicardipine has been investigated in approximately 6,000 patients, with an improvement of cognitive deterioration in more than 60% of patients treated. The pronounced anti-hypertensive activity of nicardipine and its safety and effectiveness in cognitive domain suggest its reconsideration in the treatment of cognitive impairment of vascular origin as well as for reducing the risk of recurrent stroke in patients at high risk of it.
引用
收藏
页码:808 / 826
页数:19
相关论文
共 134 条
[1]  
Abe K, 1987, Neurol Med Chir (Tokyo), V27, P819, DOI 10.2176/nmc.27.819
[2]   COMPARISON OF THE ANTICONSTRICTOR ACTION OF DIHYDROPYRIDINES (NIMODIPINE AND NICARDIPINE) AND MG2+ IN ISOLATED HUMAN CEREBRAL-ARTERIES [J].
ALBORCH, E ;
SALOM, JB ;
PERALES, AJ ;
TORREGROSA, G ;
MIRANDA, FJ ;
ALABADI, JA ;
JOVER, T .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 229 (01) :83-89
[3]   COMPARATIVE PROTECTIVE EFFECTS OF NICARDIPINE, FLUNARIZINE, LIDOFLAZINE AND NIMODIPINE AGAINST ISCHEMIC-INJURY IN THE HIPPOCAMPUS OF THE MONGOLIAN GERBIL [J].
ALPS, BJ ;
CALDER, C ;
HASS, WK ;
WILSON, AD .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 93 (04) :877-883
[4]  
ALPS BJ, 1986, BRIT J PHARMACOL, V88, P250
[5]   Protective effect of anti-hypertensive treatment on cognitive function in essential hypertension: Analysis of published clinical data [J].
Amenta, F ;
Mignini, F ;
Rabbia, F ;
Tomassoni, D ;
Veglio, F .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2002, 203 :147-151
[6]   QUANTITATIVE IMAGE-ANALYSIS STUDY OF THE CEREBRAL VASODILATORY ACTIVITY OF NICARDIPINE IN SPONTANEOUSLY HYPERTENSIVE RATS [J].
AMENTA, F ;
FERRANTE, F ;
SABBATINI, M ;
RICCI, A .
CLINICAL AND EXPERIMENTAL HYPERTENSION, 1994, 16 (03) :359-371
[7]   Vascular and neuronal hypertensive brain damage: Protective effect of treatment with nicardipine [J].
Amenta, F ;
Strocchi, P ;
Sabbatini, M .
JOURNAL OF HYPERTENSION, 1996, 14 :S29-S35
[8]   Calcium channel blockade to prevent stroke in hypertension - A meta-analysis of 13 studies with 103,793 subjects [J].
Angeli, F ;
Verdecchia, P ;
Reboldi, GP ;
Gattobigio, R ;
Bentivoglio, M ;
Staessen, AA ;
Porcellati, C .
AMERICAN JOURNAL OF HYPERTENSION, 2004, 17 (09) :817-822
[9]   BLOCKADE OF INTRACELLULAR ACTIONS OF CALCIUM MAY PROTECT AGAINST ISCHEMIC DAMAGE TO THE GERBIL BRAIN [J].
ASANO, T ;
IKEGAKI, I ;
SATOH, S ;
MOCHIZUKI, D ;
HIDAKA, H ;
SUZUKI, Y ;
SHIBUYA, M ;
SUGITA, K .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 103 (04) :1935-1938
[10]  
BARRY DI, 1993, ACTA MED SCAND, V677, P143