Literature DB >> 2949398

Calcium antagonists reduce the extent of infarction in rat middle cerebral artery occlusion model as determined by quantitative magnetic resonance imaging.

A Sauter, M Rudin.   

Abstract

The appearance and evolution of brain infarcts over 3 days following proximal occlusion of the left middle cerebral artery (MCA) in SHR rats were measured non-invasively by magnetic resonance imaging (MRI). Infarcts were clearly visible in coronal, T2 weighted brain sections, 24, 48 and 72 h after MCA occlusion in the left hemisphere, as areas of increased NMR signals. The infarcts were quantified by pixel counting in each section, the sum of 4 sections representing an accurate estimate of the total infarct size. The location and extent of infarction, determined by MRI, were found to be highly reproducible and correlated well with post-mortem histological and biochemical data. A neurological score, made every 24 h, paralleled the evolution of the infarct size, which culminated after 48 h. Pre- or post-treatment of MCA occluded rats with the dihydropyridine calcium antagonist PN 200-110 resulted in a substantial reduction of infarct size, determined by MRI 24, 48 and 72 h after infarction, compared to vehicle treated controls. These findings were corroborated by corresponding improvements of the neurological scores as well as histological and biochemical data. Post-treatment with nimodipine showed qualitatively similar effects. These results support the notion that calcium antagonists, through vascular and/or metabolic mechanisms, are effective in treating acute stroke. Since they were obtained in a chronic, relevant model of stroke with a method directly applicable also to humans, they should encourage further clinical studies with calcium antagonists.

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Year:  1986        PMID: 2949398     DOI: 10.1161/01.str.17.6.1228

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  11 in total

1.  Effect of nicardipine on somatosensory evoked potentials in patients with acute cerebral infarction.

Authors:  L P Yao; D Y Ding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-10       Impact factor: 10.154

Review 2.  Nuclear magnetic resonance in clinical pharmacology and measurement of therapeutic response.

Authors:  W H Aellig
Journal:  Br J Clin Pharmacol       Date:  1990-02       Impact factor: 4.335

Review 3.  Pharmacology of the calcium antagonist isradipine.

Authors:  U T Rüegg; R P Hof
Journal:  Drugs       Date:  1990       Impact factor: 9.546

4.  Isradipine in patients with acute ischaemic cerebral infarction. An overview of the ASCLEPIOS Programme.

Authors:  A Azcona; X Lataste
Journal:  Drugs       Date:  1990       Impact factor: 9.546

Review 5.  Experimental studies with isradipine in stroke.

Authors:  A Sauter; M Rudin
Journal:  Drugs       Date:  1990       Impact factor: 9.546

Review 6.  Isradipine. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in cardiovascular disease.

Authors:  A Fitton; P Benfield
Journal:  Drugs       Date:  1990-07       Impact factor: 9.546

7.  Effects of isradipine on methamphetamine-induced changes in attentional and perceptual-motor skills of cognition.

Authors:  Bankole A Johnson; John D Roache; Nassima Ait-Daoud; Christopher Wallace; Lynda T Wells; Yanmei Wang
Journal:  Psychopharmacology (Berl)       Date:  2004-09-25       Impact factor: 4.530

8.  Temporal evolution of focal cerebral ischemia in the rat assessed by T2-weighted and diffusion-weighted magnetic resonance imaging.

Authors:  H B Verheul; J W Berkelbach van der Sprenkel; C A Tulleken; K S Tamminga; K Nicolay
Journal:  Brain Topogr       Date:  1992       Impact factor: 3.020

9.  Photochemically-induced cerebral infarction in the rat: comparison of NMR imaging and histologic changes.

Authors:  J Verlooy; J Van Reempts; G Peersman; F Van de Vyver; B Van Deuren; M Borgers; P Selosse
Journal:  Acta Neurochir (Wien)       Date:  1993       Impact factor: 2.216

Review 10.  Isradipine. An update of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in the treatment of mild to moderate hypertension.

Authors:  R N Brogden; E M Sorkin
Journal:  Drugs       Date:  1995-04       Impact factor: 9.546

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