Statins induce angiogenesis, neurogenesis, and synaptogenesis after stroke.

Abstract:

:We demonstrate that the 3-hydroxy-3-methyl-glutaryl-coenzyme A (HMG-CoA) reductase inhibitors atorvastatin and simvastatin enhance functional outcome and induce brain plasticity when administered after stroke to rats. With atorvastatin treatment initiated 1 day after stroke, animals exhibited significant increases in vascular endothelial growth factor, cyclic guanosine monophosphate, angiogenesis, endogenous cell proliferation and neurogenesis, and an increase in the synaptic protein, synaptophysin. Atorvastatin-induced angiogenesis in a tube formation assay was reduced by an antibody against the vascular endothelial growth factor receptor 2 (FIK-1) and by the nitric oxide synthase inhibitor, N-mono-methyl-L-arginine (L-NAME). Atorvastatin also induced phosphorylation of Akt and Erk in cultured primary cortical neurons. These data indicate that atorvastatin induced brain plasticity and has neurorestorative activity after experimental stroke.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Chen J,Zhang ZG,Li Y,Wang Y,Wang L,Jiang H,Zhang C,Lu M,Katakowski M,Feldkamp CS,Chopp M

doi

10.1002/ana.10555

keywords:

subject

Has Abstract

pub_date

2003-06-01 00:00:00

pages

743-51

issue

6

eissn

0364-5134

issn

1531-8249

journal_volume

53

pub_type

杂志文章
  • NMDAR Antibodies Alter Dopamine Receptors and Cause Psychotic Behavior in Mice.

    abstract:OBJECTIVE:The aim was to demonstrate that antibodies from patients with anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis alter the levels of dopamine 1 receptor (D1R) and dopamine 2 receptor (D2R) and cause psychotic-like features in mice. METHODS:Cultured rat hippocampal neurons were treated with cerebrospinal...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25829

    authors: Carceles-Cordon M,Mannara F,Aguilar E,Castellanos A,Planagumà J,Dalmau J

    更新日期:2020-09-01 00:00:00

  • Free amino acid levels in amyotrophic lateral sclerosis.

    abstract::To evaluate reports of abnormal levels of free amino acids (AA) in patients with amyotrophic lateral sclerosis (ALS), we studied serum, cerebrospinal fluid, and urine AA in 12 patients with ALS and 12 controls matched for age, sex, and severity of disability. ALS patients had statistically significant elevations in se...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410030405

    authors: Patten BM,Harati Y,Acosta L,Jung SS,Felmus MT

    更新日期:1978-04-01 00:00:00

  • Devic's neuromyelitis optica: a clinicopathological study of 8 patients.

    abstract::We report the clinical, imaging, and laboratory features of 8 patients with Devic's neuromyelitis optica. All patients had severe myelopathy and optic neuritis. In no patient was the brain, the brainstem, or the cerebellum affected, even after several years of disease. Various immunosuppressive treatments failed to be...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410340211

    authors: Mandler RN,Davis LE,Jeffery DR,Kornfeld M

    更新日期:1993-08-01 00:00:00

  • Quantitative Separation of Tremor and Ataxia in Essential Tremor.

    abstract:OBJECTIVE:This study addresses an important problem in neurology, distinguishing tremor and ataxia using quantitative methods. Specifically, we aimed to quantitatively separate dysmetria, a cardinal sign of ataxia, from tremor in essential tremor (ET). METHODS:In Experiment 1, we compared 19 participants diagnosed wit...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25781

    authors: Casamento-Moran A,Yacoubi B,Wilkes BJ,Hess CW,Foote KD,Okun MS,Wagle Shukla A,Vaillancourt DE,Christou EA

    更新日期:2020-08-01 00:00:00

  • Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis.

    abstract::We registered 366 families in a study of dominantly inherited amyotrophic lateral sclerosis. Two hundred ninety families were screened for mutations in the gene encoding copper-zinc cytosolic superoxide dismutase (SOD1). Mutations were detected in 68 families. The most common SOD1 mutation is an alanine for valine sub...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410410212

    authors: Cudkowicz ME,McKenna-Yasek D,Sapp PE,Chin W,Geller B,Hayden DL,Schoenfeld DA,Hosler BA,Horvitz HR,Brown RH

    更新日期:1997-02-01 00:00:00

  • Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia.

    abstract::Splice-site and missense mutations have been identified in tau associated with frontotemporal dementia with parkinsonism linked to chromosome 17. In this study we assessed the genetic contribution of tau mutations to three patient series with non-Alzheimer's (non-AD) degenerative dementia. The groups included (1) a co...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/1531-8249(199908)46:2<243::aid-ana14>3.0.c

    authors: Houlden H,Baker M,Adamson J,Grover A,Waring S,Dickson D,Lynch T,Boeve B,Petersen RC,Pickering-Brown S,Owen F,Neary D,Craufurd D,Snowden J,Mann D,Hutton M

    更新日期:1999-08-01 00:00:00

  • Congenital lymphocytic choriomeningitis virus infection: spectrum of disease.

    abstract:OBJECTIVE:Lymphocytic choriomeningitis virus (LCMV) is a human pathogen and an emerging neuroteratogen. When the infection occurs during pregnancy, the virus can target and damage the fetal brain and retina. We examined the spectrum of clinical presentations, neuroimaging findings, and clinical outcomes of children wit...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.21161

    authors: Bonthius DJ,Wright R,Tseng B,Barton L,Marco E,Karacay B,Larsen PD

    更新日期:2007-10-01 00:00:00

  • Alzheimer's disease and Parkinson's disease: distinct entities or extremes of a spectrum of neurodegeneration?

    abstract::Alzheimer's disease (AD) and Parkinson's disease (PD) are generally considered to be separate and distinct disease entities. However, a considerable amount of evidence demonstrates that these disorders share common clinical and neuropathologic features and that overlap between the two conditions is extensive. For exam...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410440705

    authors: Perl DP,Olanow CW,Calne D

    更新日期:1998-09-01 00:00:00

  • Linking MRI postprocessing with magnetic source imaging in MRI-negative epilepsy.

    abstract:OBJECTIVE:MRI-negative (MRI-) pharmacoresistant focal epilepsy (PFE) patients are most challenging for epilepsy surgical management. This study utilizes a voxel-based MRI postprocessing technique, implemented using a morphometric analysis program (MAP), aiming to facilitate detection of subtle focal cortical dysplasia ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24169

    authors: Wang ZI,Alexopoulos AV,Jones SE,Najm IM,Ristic A,Wong C,Prayson R,Schneider F,Kakisaka Y,Wang S,Bingaman W,Gonzalez-Martinez JA,Burgess RC

    更新日期:2014-05-01 00:00:00

  • Expanded disability status scale progression assessment heterogeneity in multiple sclerosis according to geographical areas.

    abstract::Using placebo data from 3 randomized multiple sclerosis (MS) trials with uniform inclusion criteria, we investigated heterogeneity of Expanded Disability Status Scale (EDSS) progression by geographical areas. Our analysis revealed a significantly lower EDSS progression in Eastern European countries (10.8%) compared wi...

    journal_title:Annals of neurology

    pub_type: 杂志文章,meta分析

    doi:10.1002/ana.25323

    authors: Bovis F,Signori A,Carmisciano L,Maietta I,Steinerman JR,Li T,Tansy AP,Sormani MP

    更新日期:2018-10-01 00:00:00

  • Cortical areas differentially involved in multiplication and subtraction: a functional magnetic resonance imaging study and correlation with a case of selective acalculia.

    abstract::A patient with an intracranial hemorrhage showed differential impairment among arithmetic types (impaired in multiplication but not in subtraction). A functional magnetic resonance imaging (fMRI) experiment using normal volunteers also revealed a differential activation between the two arithmetic types. The fMRI resul...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Lee KM

    更新日期:2000-10-01 00:00:00

  • Cardiovascular health through young adulthood and cognitive functioning in midlife.

    abstract:OBJECTIVE:A study was undertaken to examine the association between overall cardiovascular health as recently defined by the American Heart Association in young adulthood to middle age and cognitive function in midlife. Overall ideal cardiovascular health incorporates 7 metrics, including the avoidance of overweight or...

    journal_title:Annals of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1002/ana.23836

    authors: Reis JP,Loria CM,Launer LJ,Sidney S,Liu K,Jacobs DR Jr,Zhu N,Lloyd-Jones DM,He K,Yaffe K

    更新日期:2013-02-01 00:00:00

  • Duodenal and gastric delivery of levodopa in parkinsonism.

    abstract::To clarify the influence of gastric emptying on levodopa-related motor fluctuations in Parkinson's disease, we assessed mobility and plasma levodopa concentrations in 10 patients during five modes of levodopa administration: (1) standard intermittent oral (SIO), (2) intermittent duodenal (ID), (3) continuous duodenal ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410230611

    authors: Kurlan R,Nutt JG,Woodward WR,Rothfield K,Lichter D,Miller C,Carter JH,Shoulson I

    更新日期:1988-06-01 00:00:00

  • Immunocytochemical observations on the distribution of myelin-associated glycoprotein and myelin basic protein in multiple sclerosis lesions.

    abstract::To study the distribution of myelin-associated glycoprotein (MAG) in human nervous tissue and in multiple sclerosis (MS) lesions, we used paraffin sections and our modification of the peroxidase-antiperoxidase technique. Sections of MS lesions also were treated with antiserum to basic protein (BP) and with histologica...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410070212

    authors: Itoyama Y,Sternberger NH,Webster HD,Quarles RH,Cohen SR,Richardson EP Jr

    更新日期:1980-02-01 00:00:00

  • Regional variation in brain lactate in Leigh syndrome by localized 1H magnetic resonance spectroscopy.

    abstract::Localized water-suppressed 1H magnetic resonance spectroscopy was performed in an 11-month-old infant with Leigh syndrome. Spectra obtained from the basal ganglia, occipital cortex, and brainstem showed elevations in lactate, which were most pronounced in regions where abnormalities were seen with routine T2-weighted ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290219

    authors: Detre JA,Wang ZY,Bogdan AR,Gusnard DA,Bay CA,Bingham PM,Zimmerman RA

    更新日期:1991-02-01 00:00:00

  • Blinded positron emission tomography study of dopamine cell implantation for Parkinson's disease.

    abstract::We assessed nigrostriatal dopaminergic function in Parkinson's disease (PD) patients undergoing a double-blind, placebo-controlled surgical trial of embryonic dopamine cell implantation. Forty PD patients underwent positron emission tomography (PET) imaging with [18F]fluorodopa (FDOPA) prior to randomization to transp...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/ana.1075

    authors: Nakamura T,Dhawan V,Chaly T,Fukuda M,Ma Y,Breeze R,Greene P,Fahn S,Freed C,Eidelberg D

    更新日期:2001-08-01 00:00:00

  • Surmounting retraining limits in musicians' dystonia by transcranial stimulation.

    abstract:OBJECTIVE:Abnormal cortical excitability is evident in various movement disorders that compromise fine motor control. Here we tested whether skilled finger movements can be restored in musicians with focal hand dystonia through behavioral training assisted by transcranial direct current stimulation to the motor cortex ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24151

    authors: Furuya S,Nitsche MA,Paulus W,Altenmüller E

    更新日期:2014-05-01 00:00:00

  • Noninvasive detection of occlusive disease of the carotid siphon and middle cerebral artery.

    abstract::Recently, transcranial Doppler sonography has been introduced into clinical practice for noninvasive investigation of the large intracranial arteries. To determine its accuracy for detection of stenosing or occluding lesions, 133 consecutive patients were studied by both transcranial Doppler sonography and selective c...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410280507

    authors: Ley-Pozo J,Ringelstein EB

    更新日期:1990-11-01 00:00:00

  • Increased serum transferrin receptor concentrations in Friedreich ataxia.

    abstract::Mitochondrial iron accumulation is thought to underlie the pathophysiology of Friedreich ataxia and may occur at the expense of cytosolic iron. Decreases in cytosolic iron induce expression of the transferrin receptor, some of which is released into the serum. Here, we demonstrate that serum transferrin receptor conce...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Wilson RB,Lynch DR,Farmer JM,Brooks DG,Fischbeck KH

    更新日期:2000-05-01 00:00:00

  • Multiple sclerosis: activated cells in cerebrospinal fluid in acute exacerbations.

    abstract::Cerebrospinal fluid (CSF) lymphocytes from three young patients undergoing acute exacerbations of multiple sclerosis were studied by flow cytometry. Using a new method that simultaneously measures cell-surface antigens and the cell-cycle phase, we determined that the CSF lymphocytes in these patients were activated. T...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410180617

    authors: Noronha A,Richman DP,Arnason BG

    更新日期:1985-12-01 00:00:00

  • McArdle's disease: biochemical and molecular genetic studies.

    abstract::We have analyzed muscle biopsy specimens from 48 patients with biochemically proven phosphorylase deficiency (McArdle's disease) by sodium dodecylsulphate polyacrylamide gel electrophoresis (SDS-PAGE), immunoblotting, and immunotitration (enzyme-linked immunosorbent assay [ELISA]). Thirty-five of the 42 patients studi...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410240612

    authors: Servidei S,Shanske S,Zeviani M,Lebo R,Fletterick R,DiMauro S

    更新日期:1988-12-01 00:00:00

  • Abnormal pattern electroretinograms in patients with senile dementia of the Alzheimer type.

    abstract::Patients with senile dementia of the Alzheimer type frequently have difficulty performing visual tasks. These difficulties may be due, at least partially, to degenerative changes in both the primary visual pathway and the visual association areas. To determine whether retinal ganglion cell dysfunction contributes to v...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410260208

    authors: Trick GL,Barris MC,Bickler-Bluth M

    更新日期:1989-08-01 00:00:00

  • Appropriate number of plasma exchanges in Guillain-Barré syndrome. The French Cooperative Group on Plasma Exchange in Guillain-Barré Syndrome.

    abstract::Plasma exchange (PE) is the standard treatment in Guillain-Barré syndrome (GBS) patients who have lost the ability to walk. The effect of exchanges before this stage and the optimal number of exchanges for the other patients are still unknown. We randomized 556 GBS patients according to severity and number of exchange...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章,多中心研究,随机对照试验

    doi:10.1002/ana.410410304

    authors:

    更新日期:1997-03-01 00:00:00

  • Imaging correlates of decreased axonal Na+/K+ ATPase in chronic multiple sclerosis lesions.

    abstract:OBJECTIVE:Degeneration of chronically demyelinated axons is a major cause of irreversible neurological decline in the human central nervous system disease, multiple sclerosis (MS). Although the molecular mechanisms responsible for this axonal degeneration remain to be elucidated, dysfunction of axonal Na+/K+ ATPase is ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.21381

    authors: Young EA,Fowler CD,Kidd GJ,Chang A,Rudick R,Fisher E,Trapp BD

    更新日期:2008-04-01 00:00:00

  • Infantile spasms: II. Lenticular nuclei and brain stem activation on positron emission tomography.

    abstract::Infantile spasms are generalized seizures specific to early infancy, and are believed to result from complex cortical-subcortical interactions during a critical period of development. We used positron emission tomography (PET) to determine local cerebral metabolic rates for glucose (1CMRG1c) in 44 infants with spasms,...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410310212

    authors: Chugani HT,Shewmon DA,Sankar R,Chen BC,Phelps ME

    更新日期:1992-02-01 00:00:00

  • Sequence-dependent and independent inhibition specific for mutant ataxin-3 by small interfering RNA.

    abstract::In Machado-Joseph disease (MJD) gene, there is a C/G polymorphism immediately after the CAG repeat; the expanded CAG repeat tract is exclusively followed by C, whereas about half of wild-type alleles are followed by G. Using this C/G polymorphism, we have engineered the small interfering RNA (siRNA) which decreased th...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20141

    authors: Li Y,Yokota T,Matsumura R,Taira K,Mizusawa H

    更新日期:2004-07-01 00:00:00

  • Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues.

    abstract::We report biochemical, immunological, and morphological findings in a patient with fatal Kearns-Sayre syndrome. Histochemical and biochemical findings from muscle biopsy specimens obtained 7 years apart documented the disease's evolution from a mild mitochondrial disorder affecting a small proportion of muscle fibers ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410210607

    authors: Bresolin N,Moggio M,Bet L,Gallanti A,Prelle A,Nobile-Orazio E,Adobbati L,Ferrante C,Pellegrini G,Scarlato G

    更新日期:1987-06-01 00:00:00

  • Abnormalities of the nucleus basalis in Down's syndrome.

    abstract::One of the most striking manifestations of Down's syndrome is profound mental retardation. Furthermore, after 35 years of age, many patients with Down's syndrome develop clinical and pathological features of Alzheimer's disease. Since brains of patients with Alzheimer's disease show significant loss of neurons in the ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410180306

    authors: Casanova MF,Walker LC,Whitehouse PJ,Price DL

    更新日期:1985-09-01 00:00:00

  • Genome-wide variant by serum urate interaction in Parkinson's disease.

    abstract:OBJECTIVE:Serum urate levels have been associated with risk for and progression of Parkinson's disease (PD). Urate-related compounds are therapeutic candidates in neuroprotective efforts to slow PD progression. A urate-elevating agent is currently under investigation as a potential disease-modifying strategy in people ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24504

    authors: Nazeri A,Roostaei T,Sadaghiani S,Chakravarty MM,Eberly S,Lang AE,Voineskos AN

    更新日期:2015-11-01 00:00:00

  • Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family.

    abstract::We describe a French amyotrophic lateral sclerosis (ALS) family with two distinct mutations in the Cu/Zn superoxide dismutase (SOD1) gene. The D90A mutation has been well described and clearly shown to cause recessive ALS. In this family, affected individuals are heterozygous for the D90A mutation and also carry a sin...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/1531-8249(20010201)49:2<267::aid-ana51>3.0

    authors: Hand CK,Mayeux-Portas V,Khoris J,Briolotti V,Clavelou P,Camu W,Rouleau GA

    更新日期:2001-02-01 00:00:00