Iron deposition and Parkinson disease / 中华行为医学与脑科学杂志

Iron is an essential metal element for human body. It is involved in many important biological metabolic processes. Iron metabolism in the central nervous system has a strict regulatory mechanism. Iron deposition occurs when the homeostasis of iron metabolism is disrupted, leading to an increase in neuronal iron uptake and a decrease in iron discharge. Aging cells develop specific iron deposition, and excessive iron produce reactive oxygen species, which can damage DNA. Highly reactive aldehydes result in irreversible modification of proteins. Stored proteins were stimulated to release iron, which in turn produces more reactive oxygen species, ultimately leading to iron-mediated cell death and neurological dysfunction. The widely used methods for assessing iron deposition include susceptibility weighted imaging and quantitative susceptibility mapping. Abnormally elevated brain iron deposition has been observed in a variety of central nervous system diseases, especially in Parkinson disease. Iron deposition plays an important role in early diagnosis, differential diagnosis, disease evaluation and monitoring and therapeutic effect evaluation of Parkinson disease. This article reviews the research progress of iron deposition in Parkinson disease.

Research progress of biomimetic nano drug delivery system in nervous system disease / 药学学报

Brain delivery of drugs remains challenging due to the presence of the blood-brain barrier (BBB). With advances in nanotechnology and biotechnology, new possibilities for brain-targeted drug delivery have emerged. Biomimetic nano drug delivery systems with high brain-targeting and BBB-penetrating capabilities, along with good biocompatibility and safety, can enable 'invisible' drug delivery. In this review, five different types of biomimetic strategies are presented and their research progress in central nervous system disorders is reviewed. Finally, the challenges and future prospects for biomimetic nano drug delivery systems in intracerebral drug delivery are summarized.

Research progress of lncRNA, miRNA and circRNA in central nervous system diseases / 医学研究生学报

Regulatory noncoding RNA (ncRNA), mainly including long noncoding RNA (lncRNA), microRNA (miRNA) and circular RNA (circRNA), is one of the research hotspots at home and abroad in recent years. Numerous studies have shown that LncRNA, miRNA and circRNA are significantly differentially expressed and play an important role in central nervous system diseases, which may become the potential targets for novel diagnostic markers and for the treatment of diseases. In this paper, the differential expression, possible mechanism and the latest research progress of lncRNA, miRNA and circRNA in central nervous system diseases are reviewed in order to provide reference for further research.

Meningoencephalitis due to Naegleria fowleri in cattle in southern Brazil / Meningoencefalite por Naegleria fowleri em um bovino no sul do Brasil

Abstract Naegleria fowleri is a free-living amoeba commonly found in the environment, mainly in fresh water and soil. This protozoon is occasionally involved in cases of fatal central nervous system disease in humans and other animal species. We describe here a case of meningoencephalitis due to Naegleria fowleri in cattle, in southern Brazil. A four-year-old Angus cow presented a clinical history of initial mild neurological signs that progressed to paddling movements, opisthotonus and lateral recumbency after five days. This animal had been kept in an irrigated rice stubble paddock. Grossly, the main lesions consisted of multiple areas of malacia in the right olfactory bulb, piriform lobes, hippocampus, frontal lobe cortex and fornix, along with severe thickening of the mesencephalon and rhombencephalon leptomeninges. Microscopically, severe multifocal necrosuppurative and hemorrhagic meningoencephalitis associated with a large quantity of amoebic trophozoites was present. The latter were confirmed to be Naegleria spp., through immunohistochemistry. Based on the strong congruence with the histopathological data of known cases reported in the literature, a probable association with Naegleria fowleri was established. To our knowledge, this is only the second report of Naegleria fowleri-associated meningoencephalitis in cattle in South America, and it is the first in southern Brazil.

Resumo Naegleria fowleri é uma ameba de vida livre, comumente encontrada no meio ambiente, principalmente em água doce e no solo. Este protozoário é ocasionalmente associado a casos fatais de doença do sistema nervoso central em seres humanos e espécies animais. No presente trabalho, um caso de meningoencefalite por Naegleria fowleri em um bovino na região sul do Brasil é descrito. Uma vaca Angus, de quatro anos de idade apresentou histórico clínico caracterizado inicialmente por sinais neurológicos leves que progrediram para movimentos de pedalagem, opistótono e decúbito lateral após cinco dias. Este animal era mantido em um piquete em resteva de arroz irrigado. Macroscopicamente, as principais lesões foram caracterizadas por múltiplas áreas de malacia no bulbo olfatório direito, lobos piriformes, hipocampo, córtex do lobo frontal e no fórnix, bem como acentuado espessamento das leptomeninges do mesencéfalo e rombencéfalo. Microscopicamente, meningoencefalite necrossupurativa e hemorrágica associada à grande número de trofozoítos amebianos foram observadas. Estes foram confirmados como Naegleria spp. através de imuno-histoquímica. Baseado na forte congruência apresentada entre os dados histopatológicos provenientes de casos conhecidos publicados na literatura, uma provável associação com Naegleria fowleri foi estabelecida. O presente trabalho trata-se do segundo relato de meningoencefalite associada à Naegleria fowleri em bovinos na América do Sul e o primeiro na região sul do Brasil.

Progress of astrocytes and their exosomes in central nervous system disease / 国际儿科学杂志

Astrocytes exist in the central nervous system widely, through cell-cell communication in neurovascular units, playing an important role in providing metabolic support for neurons, regulating nerve function and plasticity and so on.There is evidence that exosomes play a key regulatory role in intercellular communication by carrying natural cargo molecules and participate in a variety of pathophysiological processes.However, the role of astrocyte-derived exosome in central nervous system diseases is largely unknown.In this paper, the classification, characteristics, biomarkers, physiological functions, functions of astrocyte-derived exosome and their roles in central nervous system diseases are reviewed, for a deeper understanding of the role of astrocytes in central nervous system diseases.

Progress of astrocytes and their exosomes in central nervous system disease / 国际儿科学杂志

Astrocytes exist in the central nervous system widely,through cell-cell communication in neurovascular units,playing an important role in providing metabolic support for neurons,regulating nerve function and plasticity and so on.There is evidence that exosomes play a key regulatory role in intercellular communication by carrying natural cargo molecules and participate in a variety of pathophysiological processes.However,the role of astrocyte-derived exosome in central nervous system diseases is largely unknown.In this paper,the classification,characteristics,biomarkers,physiological functions,functions of astrocyte-derived exosome and their roles in central nervous system diseases are reviewed,for a deeper understanding of the role of astrocytes in central nervous system diseases.

Doenças do sistema nervoso central de bezerros no sul do Rio Grande do Sul: uma contribuição ao diagnóstico diferencial / Central nervous system disease of calves in southern Brazil: a contribution to the differential diagnosis

Este estudo teve o objetivo de determinar a frequência das enfermidades do sistema nervoso central que afetam bezerros até 12 meses de idade na região sul do Rio Grande do Sul. Foi realizado um estudo retrospectivo estabelecendo-se as principais enfermidades observadas nesta categoria de bovinos em um período de 36 anos. Foram revisados os protocolos de necropsia e de materiais remetidos ao Laboratório Regional de Diagnóstico da Faculdade de Veterinária da Universidade Federal de Pelotas entre janeiro de 1978 e dezembro de 2015 referentes aos bovinos até 12 meses de idade que apresentavam sinais neurológicos. Foram resgatados os dados epidemiológicos referentes à procedência dos animais, tipo de criação, raça, idade e época de ocorrência e frequência de cada enfermidade. Foram identificados 615 casos de bovinos com sinais neurológicos, dos quais 162 (26,3%) tinham até 12 meses de idade. Os diagnósticos foram agrupados por etiologia, sendo que as enfermidades virais totalizaram 42,6% dos casos; as doenças bacterianas 19,1% e as doenças parasitárias 17,3%. Os defeitos congênitos e as doenças hereditárias representaram 6,2% dos casos, seguidos pelas intoxicações e micotoxicoses com 4,9%; pelas doenças carenciais e multifatoriais ambas com 2,5% dos casos e pelos traumatismos com 1,9%, doenças degenerativas e neoplasias com 0,6% dos diagnósticos. Os casos inconclusivos representaram 1,86% do total. Nos bezerros até os 90 dias as principais enfermidades foram os defeitos congênitos e as meningites e encefalites por causas bacterianas, além dos abscessos do sistema nervoso central; nos bezerros entre os quatro e nove meses as enfermidades tiveram uma frequência mais baixa destacando-se apenas a raiva. A partir dos 10 até os 12 meses a babesiose, a raiva e a encefalite por herpesvírus bovino foram as mais importantes como causa de morte.(AU)

This paper aimed to determine the frequency of diseases of the central nervous system affecting calves under 12 months of age in southern Rio Grande do Sul. A retrospective study was conducted determining the main diseases observed in this category of cattle over a period of 36 years. We reviewed all the necropsy protocols and materials sent to the laboratory between 1978 and December 2015 relating to cattle under 12 months of age that showed neurological signs. The epidemiological data concerning the origin of the animals, raising system, breed, age and time of occurrence of each disease and frequency were taken from necropsy protocols. Out of 615 cases with neurological signs, 162 (26.3%) corresponded to cattle with age up to 12 months. The diagnoses were grouped by etiology of viral diseases (42.6%), bacterial diseases (19.1%), parasitic diseases (17.3%), congenital defects, hereditary diseases (6.2%), poisoning, mycotoxicoses (4.9%), nutritional deficiency and multifactorial diseases (2.5%), and trauma, degenerative diseases and neoplasms with 0.62% of diagnoses. Inconclusive cases represented 1.9% of the total diagnosed. In 1 to 90 day-old calves the main diseases observed were congenital defects, meningitis and encephalitis caused by bacteria. Central nervous system abscesses were also observed. In 4 to 9 month-old calves a lower frequency of disease were noted. Rabies was the most important disease diagnosed in this category. Babesiosis, rabies and encephalitis by bovine herpesvirus were the most important causes of death in 10 to 12 month-old calves.(AU)

Disease spectrum and prognostic factors of 499 cases of acquired immune deficiency syndrome complicated with central nervous system infections in Chongqing / 中华传染病杂志

Objective To describe the disease spectrum,morbidity,mortality and prognostic factors of acquired immune deficiency syndrome (AIDS) patients complicated with central nervous system (CNS) infections.Methods The data of 4 426 AIDS patients from February 2013 to February 2017 in Chongqing public health medical center were collected,among which 499 cases had CNS infection.The morbidity and mortality of CNS infections were calculated.Association between different CNS infections and CD4+T cell counts was analyzed.Prognostic factors for the outcome of hospitalization were also studied.Mann-Whitney U test was used for continuous variables.Univariate and multivariate analyses were performed by logistic regression analysis.Results The morbidity of CNS infections in AIDS patients was 11.27％ (499/4 426).The most prevalent CNS infections were tuberculous meningitis (4.50％),cryptococcal meningitis (3.25 ％) and CNS infections with unknown etiology (1.11 ％).The mortality rate was 18.84％ (94/499),among which tuberculous meningitis accounted for 35 cases (17.59％),cryptococcal meningitis 23 cases (15.79％) and CNS infections with unknown etiology 19 cases (38.76％).The average CD4-T cell count level in those who died were significantly lower than that in those who survived (Z=2.51,P =0.001).Visual impairment,nuchal rigidity,positive pathologic reflexes,consciousness disturbance,CD4+T cell counts＜50 cells/μL and HIV RNA≥5 lg copies/mL at baseline were independent prognostic factors for mortality.Conclusions The morbidity and mortality of CNS infections are high among AIDS patients in Chongqing,and those patients with severe immunosuppression are usually affected.Older age,consciousness disturtance and severe immunosuppression are three independent risk factors for mortality.

Research progress on the application of zebrafish in central nervous system diseases / 中国实验动物学报

As a new model animal, zebrafish has been widely used in the research of the development and disease related to various organs, such as nervous, cardiovascular, digestive and hemopoietic system. Central nervous system ( CNS) disease is one of the leading causes of death and disability worldwide. There is still lacking of effective therapeutic strategies to treat most of the CNS diseases, due to the low ability of self-regeneration and recovery of the neurons after injury. In recent years, zebrafish has been proved to be an ideal vertebrate model to study some of the CNS diseases because their genetic physiology and other features are closed and similar to humans. The application of zebrafish in CNS diseases has contributed largely on understanding the mechanisms and on the therapy of CNS diseases. This review summarizes the recent progress of the applications of zebrafish on the study of CNS diseases.

Effect of animal medicines for "extinguishing wind to arrest convulsions" on central nervous system diseases / 中国中药杂志

The human health is seriously affected by central nervous system(CNS) diseases, but the pathogenesis of CNS diseases is still not completely clear. Currently, the drugs used to treat CNS diseases are mainly receptor modulators and neurotransmitter inhibitors, which have serious side effects; and there are short of drugs for treating CNS diseases clinically. Studies suggest that animal medicines mainly include protein, polypeptide and small-molecule compounds, and have such pharmacological effects in calming, resisting convulsions and improving brain tissues. Plenty of studies suggest that animal medicines usually have a strong activity and good curative effect on these diseases, with a promising prospect in research and development of drugs treating CNS diseases. Based on systematic reviews of literatures, this paper summarizes active ingredients and main pharmacological effects of animal medicines in "extinguishing wind to arrest convulsions" for the CNS diseases, epilepsy and cerebral ischemia, and discusses their study value and application prospects. The results showed that the studies of protein and peptides were relatively simple, and some animal medicines were still blank. The authors believed that amino acids and small molecular compounds should be transferred to oligopeptide, advanced protein extraction and separation techniques shall be adopted for identifying the protein polypeptide composition structure and studying the efficacy, and the methods of biological technology were used to develop peptide biological products for the treatment of CNS diseases. This paper could provide ideas and reference for developing animal medicine products for the treatment of CNS diseases.

Advance in Intestinal Flora Affecting Central Nervous System Diseases (review) / 中国康复理论与实践

@# Intestinal flora plays an important role in the process of human health and disease conversion. It not only participates in a number of physiological processes in the host, but also affects the central nervous system (CNS) -related diseases, which may involve in neurotransmitter, immune, endocrine, metabolites, etc. Intestinal dysbacteriosis plays a role in the development of CNS diseases, such as ischemic brain injury, Parkinson's disease, Alzheimer's disease, multiple sclerosis, hepatic encephalopathy, and mental disorders, etc. Fecal microbes transplantation, exercise training, acupuncture and Tuina therapy can improve the intestinal flora balance, which may be potential for the treatment and prevention of some nervous system diseases.

Research progresses and function of the cannabinoid receptor 2 in the central nervous system diseases / 国际儿科学杂志

Cannabinoid receptor (CBR) has two subtypes,type 1 cannabinoid receptor (CB 1 receptor,CB1R) and type 2 cannabinoid receptor(CB2 receptor,CB2R).CB2R widely is found distributing in the central nervous system and playing important functions.Cannabis can regulate CB2R signal pathway to protect central nervous system in CNS diseases.

Updates on gap junctions in central nervous system diseases / 国际儿科学杂志

Gap junctions play an important role in cell growth,development,differentiation,the transmission of nerve impulses and homeostasis.Increase or decrease in gap junctions may cause neurological dysfunctions,such as Alzheimer's disease,demyelinating disease,epilepsy,glioma,hypoxic ischemic encephalopathy.Therefore,research on gap junctions may provide important clues to understand demyelinating diseases,neural stem cell transplantation and post-iniury restoration.

Effects of N-acyl glucosamines on GABA uptake activity of GABA transporter 1 / 中国药科大学学报

@#In order to screen the inhibitors of GAT1 protein, the effects of synthetic N-acylglucosamines on the GABA uptake activity of GAT1 were examined in the HEK-293 cell model stably expressing GAT1 by performing GABA uptake assay. And since the N-linked oligosaccharides, especially their terminal sialic acid of GAT1 are necessary for the function of GAT1, their effects on the modification of N-glycans of GAT1 were also determined by the quantitative analysis of the sialic acid of GAT1. The results showed that 10 mmol /L 3-O-methyl-N-acetylglucosamine(3-O-Met-GlcNAc)reduced the GABA uptake activity of GAT1 to 53%(P< 0. 01)through inhibiting the sialylation of GAT1(66. 8%). And the GABA uptake activities were decreased to 54%, 63%, 63% and 67%(P< 0. 01), respectively, by the treatments of 10 mmol /L N-propionylglucosamine(GlcNProp), N-hexanoylglucosamine(GlcNHex), N-cycloproylgormylglucosamine(GlcNCyclo)and N-acetamidoacetylglucosamine(GlcNAc-acetamido)through inhibiting N-glycan trimming. These results indicate that the analogues of glucosamines have great potential in the development of inhibitors of GAT1 activity or sialic acid biosynthesis.

Clinical diagnosis and treatment of inflammatory granuloma in central nervous system / 中国基层医药

Objective To discuss the diagnosis and treatment of inflammatory granuloma in central nervous system(CNS)to provide reference for clinic.Methods Retrospective data included 8 patients with CNS inflammatory granuloma in Department of Neurosurgery,Shanxi People's Hospital,2012 -2015.We analyzed the imaging features, postoperative symptoms,blood and cerebrospinal fluid changes and prognosis.Results 8 cases all received surgical treatment.All the symptoms were improved,and the CT showed that the lesions were disappeared.All the patients had recovered to normal life and work.Conclusion The diagnosis of CNS inflammatory granuloma is difficult.Clinical manifestations are lack of specificity.The blood and cerebrospinal fluid laboratory examination have no abnormal changes.CT and MRI are the main diagnostic methods.Postoperative pathology is the gold standard for diagnosis.The large lesion,frequent episodes of epilepsy,severe neurological deficits and possibility of brain tumor all should be treated by surgery.

Research on AQP4 and central nervous system diseases / 国际儿科学杂志

Aquaporins (AQP) are membrane channel proteins which facilitate water transport through cell membranes.AQP4 is abundantly expressed in brain which is located in endfeet of astrocytes adjacent to capillaries,neurons,and neuronal synapses.It has also been identified in neurons of the supraoptic and paraventricular nuclei of the hypothalamus.AQP are closely related to many central nervous system diseases.Researches have showed that AQP4 participates in regulating and controling process of cerebral edema that caused by brain trauma,cerebral ischemia,intracranial infection and mmour,etc.AQP4 antibody is specific biological markers in serum of patients with neuromyelitis,which helps diagnosis of neuromyelitis optica and multiple sclerosis,predicting prognosis and therapy of neuromyelitis optica.AQP4 has been shown to play roles in pathological and physiological process of neurodegenerative diseases,epilepsy,migraine.This article aims to review the distribution,function,influential factors of AQP4 and research development of AQP4 in common diseases of the central nervous system.

The Roles of Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand and Its Receptors in Central Nervous System Diseases / 国际脑血管病杂志

Tumor necrosis factor-related apoptosis-inducing ligand(TRAIL)is the third member of the tumor necrosis factor(TNF)superfamily.It has received much concern because of its selective killing effect on tumor cells and virus infected cells.However,the subsequent studies have suggested that TRAIL also induces normal cells,such as the death of neurons and oligodendrocytes.TRAIL is associated with a variety of central nervous system diseases including primary brain tumor,multipie sclerosis and ischemic stroke.

Short Latency Somatosensory Evoked Potentials in Evaluation of Central Nervous System Function of Patients with Coronary Cardiac Diease / 中国康复理论与实践

@#ObjectiveTo evaluate central nervous system function of patients with coronary cardiac diease by short latency somatosensory evoked potentials (SSEP).MethodsThe cerebral and spinal somatosensory evoked potentials were recorded by stimulating median nerve in 43 patients with coronary cardiac disease but without apparent nervous symptoms and 14 healthy control subjects.ResultsThe lactency periods and central conductive time of N13, N20 and P25 wave were significantly prolonged in patients with myocardial infarction (MI) or angina pectoris (AP) when compared with normal controls (P<0.05～0.001). The lactency periods and central conductive time of N20 and P25 wave recorded in MI patients were longer than those recorded in AP patients (P<0.01～0.001).ConclusionThe subclinical nervous damages in the central somatosensory pathway from spinal cord to cerebral cortex is present in patients with coronary cardiac disease especially myocardial infarction.

Expression and Regulation of Intercellular Adhesion Molecule-1 in Central Nervous System Diseases / 实用儿科临床杂志

Intercellular adhesion molecule-1 (ICAM-1) is found in surface of cells in various tissues,which is a adhesion molecule with wide range of biological activity and plays an important role in inflammatory and immune response,signal transduction,tissue repair and many other physiological and pathological processes.In this paper,ICAM-1 expression and regulation in the body,as well as some actions in the pathogenesis of central nervous system diseases are reviewed.

Clinical and CT features of Fahr disease: a report of 2 families / 中华放射学杂志

Objective To explore the clinical manifestations, CT features, and inheritance pattern of Fahr disease. Methods Head CT was scanned and serum calcium and phosphorum were measured in 14 persons from 2 families, and the 2 families' history was investigated. Results The serum calcium and phosphorum were normal in the 14 persons. There were 8 cases of Fahr disease, and the head CT showed local or diffuse calcium deposition in bilateral basal ganglia, subcortex, and thalamus, respectively. The inheritance pattern of the 8 cases of Fahr disease in the two families showed holandric inheritance, The clinical symptom and sign included seizures, irritability, mental retardation or no abnormal findings. Conclusion Fahr disease is a hereditary disease characterized by idiopathy and calcium deposition in the central nervous system. The clinical feature is various and head CT is an important examination in the diagnosis of Fahr disease.