Pressor response to intravenous tyramine in healthy subjects after safinamide, a novel neuroprotectant with selective, reversible monoamine oxidase B inhibition

被引:45
作者
Cattaneo, C
Caccia, C
Matzo, A
Maj, R
Fariello, RG
机构
[1] Newron Pharmaceut SpA, I-20091 Bresso, MI, Italy
[2] IPAS SA, Ligornetto, Switzerland
关键词
safinamide; monoamine oxidase; tyramine;
D O I
10.1097/00002826-200307000-00012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Safinamide is a novel neuroprotectant combining sodium and calcium channel blocking properties with selective, reversible monoamine oxidase type B (MAO B) inhibition. Phase I studies have demonstrated that in healthy volunteers, the ED50 (a dose that inhibits enzyme activity by 50% in 50% of treated subjects) for MAO B inhibition is 87.5 mug/kg/day orally, and that no MAO A inhibition occurs after 10-mg/kg oral dosing. To assess the risk of inducing the "cheese effect," the effect of safinamide and placebo on the pressor response to tyramine was investigated in a group of healthy male volunteers. The study was an open, single-dose placebo-controlled trial with the 2 treatments in sequence. An increase of 30 turn Hg systolic blood pressure was obtained by intravenous tyramine administered by 0.5-mg incremental boluses injected at 15-minute intervals. The amount of tyramine necessary to achieve such a blood pressure increase was the same after the safinamide 2-mg/kg oral load compared with placebo. These results suggest that dietary restrictions for food with high tyramine content should not be required under safinamide treatment.
引用
收藏
页码:213 / 217
页数:5
相关论文
共 25 条
[1]  
BIECK PR, 1989, J NEURAL TRANSM-GEN, P21
[2]  
CACCIA C, 2001, 5 INT C PROGR ALZH P
[3]   BETA-BLOCKADE ANTAGONISM OF TYRAMINE-INDUCED RISE IN BLOOD-PRESSURE [J].
COLOMBO, F ;
SEGA, R ;
MAILLAND, F ;
RIGO, R ;
PALVARINI, L ;
LIBRETTI, A .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1988, 34 (03) :263-266
[4]   EFFECT OF A NOVEL MONOAMINE-OXIDASE INHIBITOR, MOCLOBEMIDE ON THE SENSITIVITY TO INTRAVENOUS TYRAMINE AND NOREPINEPHRINE IN HUMANS [J].
CUSSON, JR ;
GOLDENBERG, E ;
LAROCHELLE, P .
JOURNAL OF CLINICAL PHARMACOLOGY, 1991, 31 (05) :462-467
[5]   Selegiline and mortality in subjects with Parkinson's disease - A longitudinal community study [J].
Donnan, PT ;
Steinke, DT ;
Stubbings, C ;
Davey, PG ;
MacDonald, TM .
NEUROLOGY, 2000, 55 (12) :1785-1789
[6]   SELECTIVE INHIBITORS OF MONOAMINE OXIDASE-A AND OXIDASE-B - BIOCHEMICAL, PHARMACOLOGICAL, AND CLINICAL PROPERTIES [J].
FOWLER, CJ ;
ROSS, SB .
MEDICINAL RESEARCH REVIEWS, 1984, 4 (03) :323-358
[7]   Possible serotonin syndrome arising from an interaction between nortriptyline and selegiline in a lady with parkinsonism [J].
Hinds, NP ;
Hillier, CEM ;
Wiles, CM .
JOURNAL OF NEUROLOGY, 2000, 247 (10) :811-811
[8]  
HINZE C, 1994, J NEURAL TRANSM-SUPP, P371
[9]   Paroxysmal hypertensive crises induced by selegiline in a patient with Parkinson's disease [J].
Ito, D ;
Amano, T ;
Sato, H ;
Fukuuchi, Y .
JOURNAL OF NEUROLOGY, 2001, 248 (06) :533-534
[10]   SOME OBSERVATIONS UPON A NEW INHIBITOR OF MONOAMINE OXIDASE IN BRAIN TISSUE [J].
JOHNSTON, JP .
BIOCHEMICAL PHARMACOLOGY, 1968, 17 (07) :1285-&