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1.
Hong Kong Med J ; 29(6): 514-523, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37968897

ABSTRACT

INTRODUCTION: The utilisation of extracorporeal membrane oxygenation (ECMO) has been rapidly increasing in Hong Kong. This study examined 10-year trends in the utilisation and clinical outcomes of ECMO in Hong Kong. METHODS: We retrospectively reviewed the records of all adult patients receiving ECMO who were admitted to the intensive care units (ICUs) of public hospitals in Hong Kong between 2010 and 2019. Temporal trends across years were assessed using the Mann-Kendall test. Observed hospital mortality was compared with the Acute Physiology and Chronic Health Evaluation (APACHE) IV-predicted mortality. RESULTS: The annual number of patients receiving ECMO increased from 18 to 171 over 10 years. In total, 911 patients received ECMO during the study period: 297 (32.6%) received veno-arterial ECMO, 450 (49.4%) received veno-venous ECMO, and 164 (18.0%) received extracorporeal cardiopulmonary resuscitation. The annual number of patients aged ≥65 years increased from 0 to 47 (27.5%) [P for trend=0.001]. The median (interquartile range) Charlson Comorbidity Index increased from 1 (0-1) to 2 (1-3) [P for trend<0.001] while the median (interquartile range) APACHE IV score increased from 90 (57-112) to 105 (77-137) [P for trend=0.003]. The overall standardised mortality ratio comparing hospital mortality with APACHE IV-predicted mortality was 1.11 (95% confidence interval=1.01-1.22). Hospital and ICU length of stay both significantly decreased (P for trend=0.011 and <0.001, respectively). CONCLUSION: As ECMO utilisation increased in Hong Kong, patients put on ECMO were older, more critically ill, and had more co-morbidities. It is important to combine service expansion with adequate resource allocation and training to maintain quality of care.


Subject(s)
Cardiopulmonary Resuscitation , Extracorporeal Membrane Oxygenation , Adult , Humans , Hong Kong , Retrospective Studies , APACHE
2.
Transfus Med ; 33(4): 315-319, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37286528

ABSTRACT

INTRODUCTION: Although no case of COVID-19 transmission through transfusion has been reported, blood transfusion service (BTS) continues to implement pre-donation and post-donation measures to minimise the risk. In year 2022, when local healthcare system was badly impacted by a major outbreak, it opened an opportunity to re-examine the viraemia risk in these asymptomatic donors. MATERIALS AND METHODS: Records were retrieved from blood donors who reported COVID-19 after donation and follow-up was also made for recipients who received their blood. Blood samples at donation were tested for SARS-CoV-2 viraemia by single-tube nested real-time RT-PCR assay designed to detect most SARS-CoV-2 variants including the prevailing delta and omicron variants. RESULTS: From 1 January to 15 August 2022, the city with 7.4 M inhabitants recorded 1 187 844 COVID-19 positive cases and 125 936 successful blood donations were received. 781 donors reported to the BTS after donation with 701 being COVID-19 related (including close contact and symptoms respiratory tract infection). 525 COVID-19 were positive at the time of call back or follow-up. Of the 701 donations, they were processed into 1480 components with 1073 discarded upon donors' call back. For remaining 407 components, no recipient was found to have adverse event or COVID-19 positive. 510 samples from the above 525 COVID-19 positive donors were available and all tested negative for SARS-CoV-2 RNA. DISCUSSION: With the negative SARS-CoV-2 RNA in blood donation samples and follow up data in transfusion recipients, the risk of transfusion transmitted COVID-19 appears negligible. However, current measures remains important in securing blood safety with ongoing surveillance of their effectiveness.


Subject(s)
COVID-19 , Humans , COVID-19/epidemiology , SARS-CoV-2 , Viremia , RNA, Viral , Blood Transfusion , Blood Donors , Disease Outbreaks
3.
Clin Kidney J ; 16(2): 285-292, 2023 Feb.
Article in English | MEDLINE | ID: mdl-36755836

ABSTRACT

Background: Current ways to diagnose citrate accumulation (CA) in patients receiving regional citrate anticoagulation (RCA) continuous renal replacement therapy (CRRT) are confounded by various clinical factors. Serum citrate measurement emerges as a more direct way to diagnose CA, but its clinical utility and optimal cut-off values remain undefined. This study examined serum citrate kinetics and its diagnostic performance for CA in patients receiving RCA CRRT. Methods: A multicentre prospective study was carried out in two tertiary referral centre intensive care units in Hong Kong with serum citrate levels measured at baseline and 2, 6, 12, 24, 36, 48 and 72 h after initiation of RCA CRRT and their relationships with the development of CA. Results: Among the 133 patients analysed, 18 patients (13.5%) developed CA. The serum citrate levels at baseline and 2, 6 and 12 h after initiation of RCA CRRT in patients who had CA were significantly higher than the non-CA group (P < .001 for all). The CA group also had higher serum citrate levels than the non-CA group {median 0.93 mmol/L [interquartile range (IQR) 0.81-1.16) versus 0.37 mmol/L (IQR 0.26-0.57), P < .001}. Using a cut-off of 0.85 mmol/L, the serum citrate level had a sensitivity of 0.77 and a specificity 0.96 for the diagnosis of CA [area under the receiver operating characteristics curve (AUROC) 0.90, P < .001]. The 2-h and 6-h serum citrate levels had good discriminatory abilities for predicting subsequent development of CA (AUROC 0.86 and 0.83 for 2-h and 6-h citrate levels using cut-off values of 0.34 and 0.63 mmol/L, respectively; P < .001). Conclusion: Serum citrate levels were significantly higher in patients with CA compared with patients without CA. Serum citrate levels showed good performance in diagnosing and predicting the development of CA.

5.
J Invest Dermatol ; 140(1): 182-190.e5, 2020 01.
Article in English | MEDLINE | ID: mdl-31247199

ABSTRACT

The bacteriophage (phage) component of the skin microbiome in patients with psoriasis has not been systematically explored. The purpose of this study is to investigate phage and bacterial components of the skin microbiome in patients with psoriasis and in healthy family controls. Lesional skin swabs of four different locations (elbow, forearm, knee, and scalp) were taken from patients with psoriasis. Healthy skin swabs of matched locations were taken from contralateral non-lesional skin and healthy family controls. Skin microbiomes were investigated using next-generation shotgun metagenomics sequencing. 81 skin microbiome samples (27 lesional skin samples and 54 healthy skin samples from contralateral non-lesional skin and family controls) obtained from 16 subjects with psoriasis and 16 matched family controls were sequenced and analyzed. Among phage species with abundant host bacteria, two significantly differential abundant phage species, Acinetobacter phage Presley and Pseudomonas phage O4 (adjusted P < 0.05), between psoriasis lesional skin and healthy skin were identified. Samples with high levels of these phage species had their host bacteria abundance suppressed (P = 0.03 and P < 0.001). Differential phage composition between lesional skin in patients with psoriasis and healthy skin from contralateral non-lesional sites and family controls, as well as the suppression of bacteria host of the respective phage, suggest possible avenues for probiotic phage therapeutics.


Subject(s)
Acinetobacter/virology , Bacteriophages/physiology , Microbiota/genetics , Pseudomonas/virology , Psoriasis/microbiology , Skin/microbiology , Adult , Aged , Female , Healthy Volunteers , High-Throughput Nucleotide Sequencing , Humans , Male , Metagenomics , Middle Aged , Psoriasis/virology , Skin/virology
7.
Int J Epidemiol ; 45(1): 64-72, 2016 Feb.
Article in English | MEDLINE | ID: mdl-25480143

ABSTRACT

The Department of Health Elderly Health Service Cohort in Hong Kong was set up to promote understanding of ageing in a global context, to exploit the role of Hong Kong as a sentinel for populations currently experiencing very rapid economic development, to provide a developed non-Western 'social laboratory' where empirically derived hypotheses can be tested and to leverage the different patterns of common chronic diseases between East and West to generate novel hypotheses about their determinants. The initial cohort enrolled from July 1998 to the end of December 2001 includes 66 820 people aged 65 years or older, forming about 9% of the population of this age. A comprehensive health assessment was made at enrollment and then repeated regularly on an ongoing basis. The health assessment included a comprehensive assessment of lifestyle, social circumstances, physical health and mental health, including an assessment of cognition and depressive symptoms. Health services use and deaths have been obtained by record linkage and confirmed, where necessary, by telephone interview. Currently, the data are not publicly available; we would welcome collaborations and research proposals.


Subject(s)
Aging , Alcohol Drinking , Comorbidity , Mortality , Obesity/epidemiology , Smoking/epidemiology , Adiposity , Aged , Aged, 80 and over , Body Mass Index , Cohort Studies , Depression/epidemiology , Female , Hong Kong/epidemiology , Humans , Life Style , Male , Risk Factors
9.
Infect Control Hosp Epidemiol ; 36(1): 87-92, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25627766

ABSTRACT

OBJECTIVE To assess the effectiveness of infection control preparedness for human infection with influenza A H7N9 in Hong Kong. DESIGN A descriptive study of responses to the emergence of influenza A H7N9. SETTING A university-affiliated teaching hospital. PARTICIPANTS Healthcare workers (HCWs) with unprotected exposure (not wearing N95 respirator during aerosol-generating procedure) to a patient with influenza A H7N9. METHODS A bundle approach including active and enhanced surveillance, early airborne infection isolation, rapid molecular diagnostic testing, and extensive contact tracing for HCWs with unprotected exposure was implemented. Seventy HCWs with unprotected exposure to an index case were interviewed especially regarding their patient care activities. RESULTS From April 1, 2013, through May 31, 2014, a total of 126 (0.08%) of 163,456 admitted patients were tested for the H7 gene by reverse transcription-polymerase chain reaction per protocol. Two confirmed cases were identified. Seventy (53.8%) of 130 HCWs had unprotected exposure to an index case, whereas 41 (58.6%) and 58 (82.9%) of 70 HCWs wore surgical masks and practiced hand hygiene after patient care, respectively. Sixteen (22.9%) of 70 HCWs were involved in high-risk patient contacts. More HCWs with high-risk patient contacts received oseltamivir prophylaxis (P=0.088) and significantly more had paired sera collected for H7 antibody testing (P<0.001). Ten (14.3%) of 70 HCWs developed influenza-like illness during medical surveillance, but none had positive results by reverse transcription-polymerase chain reaction. Paired sera was available from 33 of 70 HCWs with unprotected exposure, and none showed seroconversion against H7N9. CONCLUSIONS Despite the delay in airborne precautions implementation, no patient-to-HCW transmission of influenza A H7N9 was demonstrated.


Subject(s)
Air Microbiology , Contact Tracing , Infectious Disease Transmission, Patient-to-Professional/prevention & control , Influenza A Virus, H7N9 Subtype , Influenza, Human/transmission , Occupational Exposure/prevention & control , Population Surveillance , Adolescent , Adult , Aged , Aged, 80 and over , Antibodies, Viral/blood , Antiviral Agents/therapeutic use , Child , Child, Preschool , Cross Infection/diagnosis , Cross Infection/prevention & control , Female , Health Personnel , Hong Kong , Hospitals, Teaching/organization & administration , Humans , Infant , Infection Control/organization & administration , Influenza A Virus, H7N9 Subtype/genetics , Influenza A Virus, H7N9 Subtype/immunology , Influenza A Virus, H7N9 Subtype/isolation & purification , Influenza, Human/diagnosis , Influenza, Human/prevention & control , Male , Middle Aged , Occupational Exposure/analysis , Oseltamivir/therapeutic use , Polymerase Chain Reaction , Post-Exposure Prophylaxis , Respiratory Protective Devices , Young Adult
12.
Clin Genet ; 85(6): 562-7, 2014 Jun.
Article in English | MEDLINE | ID: mdl-23808592

ABSTRACT

Using a combination of homozygosity mapping and whole-exome sequencing (WES), we identified a novel missense c.1819G>A mutation (G607S) in the endothelin-converting enzyme-like 1 (ECEL1) gene in a consanguineous pedigree of Turkish origin presenting with a syndrome of camptodactyly, scoliosis, limited knee flexion, significant refractive errors and ophthalmoplegia. ECEL1 mutations were recently reported to cause recessive forms of distal arthrogryposis. This report expands on the molecular basis and the phenotypic spectrum of ECEL1-associated congenital contracture syndromes.


Subject(s)
Arthrogryposis/genetics , Metalloendopeptidases/genetics , Mutation, Missense , Phenotype , Adult , Arthrogryposis/pathology , Consanguinity , Exome , Female , Genotype , Homozygote , Humans , Male , Pedigree , Sequence Analysis, DNA , Turkey
13.
Hong Kong Med J ; 19 Suppl 4: 39-41, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23775186

ABSTRACT

1. Reliable and valid interviewer-administered questionnaires were developed to investigate associations of perceived neighbourhood attributes of Hong Kong older adults with their walking for transportation and recreation. 2. Access to and availability of different types of services and destinations, provision of facilities for resting/sitting in the neighbourhood, and easy access to/from residential buildings may help maintain an active lifestyle by facilitating walking for transport in the neighbourhood. 3. Access to services, indoor places for walking, environmental aesthetics, low traffic, and absence of physical barriers may promote recreational walking..


Subject(s)
Life Style , Residence Characteristics , Transportation , Walking/physiology , Aged , Aged, 80 and over , Environment Design , Female , Hong Kong , Humans , Male , Pilot Projects , Recreation , Surveys and Questionnaires
14.
Mini Rev Med Chem ; 13(2): 273-9, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22512581

ABSTRACT

This review addressed the adverse effects of the frequently-used recreational drug, ketamine through using mice and monkey models. Our laboratory has documented initially that ketamine can induce the formation of hyperphosphorlated tau (hypertau), which is a hallmark of Alzheimer's disease (AD), in the cerebral cortex of both mice and monkeys as well as apoptosis in neurons in these species. Besides the cerebral cortex, other centers in the central nervous system (CNS) and peripheral nervous system (PNS) are also influenced by ketamine. Cerebellum was found to be down-regulated in both mice and humans after long-term of ketamine administration and it was caused by the apoptosis of Purkinje cells. Deleterious effects in other organs reported in long-term ketamine users include of kidney dysfunction leading to proteinuria, fibrosis of the urinary bladder and reduction in size of the urinary bladder leading to frequent urination, increase of liver fibrosis and cardiac problems such as premature ventricular beats. Moreover, ketamine is usually co-administrated with other chemicals such as caffeine or alcohol. It has been reported increased harmful effects when ketamine was used in combination with the above substances. Mechanisms of damages of ketamine might be due to 1) up-regulation of NMDA receptors leading to overestimation of glutamatergic system or 2) the metabolite of ketamine which was a hydroquinone exerted toxicity.


Subject(s)
Alcoholic Intoxication/complications , Anesthetics, Dissociative/adverse effects , Ketamine/adverse effects , Models, Animal , Animals , Brain/drug effects , Brain/pathology , Haplorhini , Kidney/drug effects , Kidney/pathology , Liver/drug effects , Liver/pathology , Mice , Urinary Bladder/drug effects , Urinary Bladder/pathology
15.
Nucleic Acids Res ; 41(Database issue): D530-5, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23161678

ABSTRACT

The Gene Ontology (GO) Consortium (GOC, http://www.geneontology.org) is a community-based bioinformatics resource that classifies gene product function through the use of structured, controlled vocabularies. Over the past year, the GOC has implemented several processes to increase the quantity, quality and specificity of GO annotations. First, the number of manual, literature-based annotations has grown at an increasing rate. Second, as a result of a new 'phylogenetic annotation' process, manually reviewed, homology-based annotations are becoming available for a broad range of species. Third, the quality of GO annotations has been improved through a streamlined process for, and automated quality checks of, GO annotations deposited by different annotation groups. Fourth, the consistency and correctness of the ontology itself has increased by using automated reasoning tools. Finally, the GO has been expanded not only to cover new areas of biology through focused interaction with experts, but also to capture greater specificity in all areas of the ontology using tools for adding new combinatorial terms. The GOC works closely with other ontology developers to support integrated use of terminologies. The GOC supports its user community through the use of e-mail lists, social media and web-based resources.


Subject(s)
Databases, Genetic , Genes , Molecular Sequence Annotation , Vocabulary, Controlled , Internet , Phylogeny
16.
Curr Neurovasc Res ; 9(3): 167-75, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22621233

ABSTRACT

DL-3-n-Butylphthalide (NBP) is a synthetic compound based on L-3-n-Butylphthalide which was isolated from seeds of Apium graveolens. The present study aims at evaluating the outcome of NBP given prior to and after the onset of ischemic stroke in spontaneously hypertensive rats (SHR) and normotensive Wistar Kyoto rats (WKY). Stroke was induced by the middle cerebral artery occlusion (MCAO) in SHR and WKY. For pre-treatment, NBP was administered to SHR and WKY daily for two months prior to MCAO. For post-treatment, NBP was given daily for seven consecutive days after MCAO. Seven days post-surgery, rats were tested for the presence of neurological deficits. Magnetic resonance imaging (MRI) and 2,3,5-triphenyltetrazolium chloride (TTC) staining were employed to calculate the infarct volume. The cerebral cortex and corpus striatum in the ischemic penumbra area were examined microscopically for pathological changes. In SHR, NBP pre- and post-treatment significantly lowered neurological deficit scores, reduced infarct volume, and minimized pathological changes in the penumbra area when compared to oil-vehicle treated controls. In WKY, these beneficial effects were observed only in the post-treatment group. The beneficial effects of NBP post-treatment were greater in WKY than in SHR. Results indicated that NBP could exert both preventive and therapeutic effects on ischemic stroke in SHR, but only exerted therapeutic effect in WKY.


Subject(s)
Antioxidants/therapeutic use , Benzofurans/therapeutic use , Brain Injuries/pathology , Brain Injuries/prevention & control , Cerebral Cortex/blood supply , Nervous System Diseases/prevention & control , Analysis of Variance , Animals , Brain Infarction/etiology , Brain Infarction/prevention & control , Brain Injuries/etiology , Disease Models, Animal , Infarction, Middle Cerebral Artery/complications , Infarction, Middle Cerebral Artery/drug therapy , Magnetic Resonance Imaging , Male , Nervous System Diseases/etiology , Neurologic Examination , Rats , Rats, Inbred SHR , Rats, Inbred WKY , Tetrazolium Salts
17.
Hum Exp Toxicol ; 31(9): 877-86, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22354085

ABSTRACT

Ketamine is one of the common recreational drugs used in rave parties and it is frequently taken with alcohol. In spite of this, the potential toxicity of ketamine in liver and kidney has not been fully documented. In this study, ICR mice were treated for periods of 6, 16 and 28 weeks with 30 mg/kg ketamine injected daily intraperitoneally, and together with alcohol (0.5 ml of 10% alcohol for each mouse) during the last 4 weeks of the treatment periods. Our experimental results showed significant damage in liver, including fatty degeneration of liver cells, fibrosis and increase in liver glutamic oxaloacetic transaminase, proliferative cell nuclear antigen and lactate dehydrogenase after 16 weeks of treatment with ketamine. Hydropic degenerations of the kidney tubules were observed as early as 6 weeks of treatment. Long-term ketamine administration (28 weeks) led to atresia of glomeruli in the kidney. Proteinuria was confirmed in the 67% of the ketamine-treated animals after 28 weeks of treatment. It was apparent that ketamine when taken chronically (16 weeks of treatment and thereafter) affected both liver and kidney definitively. The damages in both liver and kidney of these mice were more severe when the animals were treated with both ketamine and alcohol.


Subject(s)
Anesthetics, Dissociative/toxicity , Ethanol/toxicity , Ketamine/toxicity , Kidney/drug effects , Liver/drug effects , Anesthetics, Dissociative/administration & dosage , Animals , Aspartate Aminotransferases/metabolism , Drug Synergism , Ethanol/administration & dosage , Ketamine/administration & dosage , Kidney/pathology , L-Lactate Dehydrogenase/metabolism , Liver/enzymology , Liver/pathology , Liver Cirrhosis/chemically induced , Liver Cirrhosis/enzymology , Liver Cirrhosis/pathology , Male , Mice , Mice, Inbred ICR , Proteinuria/chemically induced
18.
Hong Kong Med J ; 18 Suppl 2: 4-7, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22311352

ABSTRACT

1. A cohort of Elderly Health Centres was examined to determine whether influenza vaccination decreased hospitalisation and mortality. 2. In the influenza season, influenza vaccination reduced all-cause mortality by half and cardiorespiratory hospitalisation by a quarter. The extent to which influenza vaccination protects older people from serious morbidity and mortality needs to be confirmed in appropriately designed studies, so that scarce health care resources can be used effectively


Subject(s)
Hospitalization/statistics & numerical data , Influenza, Human/prevention & control , Vaccination/statistics & numerical data , Aged , Cardiovascular Diseases/mortality , Cause of Death , Female , Health Services for the Aged , Hong Kong/epidemiology , Humans , Male , Multivariate Analysis , Pneumonia/mortality , Poisoning/mortality , Poisson Distribution , Wounds and Injuries/mortality
19.
Neurochem Res ; 37(5): 911-9, 2012 May.
Article in English | MEDLINE | ID: mdl-22246225

ABSTRACT

3-n-Butylphthalide (NBP) is a compound extracted from Chinese celery and is used as an anti-hypertensive herbal medicine for treating stroke patients. The aim of this study is to demonstrate the effects and mechanisms of this compound through in vitro and in vivo experiments. Culture experiments were performed by adding hydrogen peroxide (H(2)O(2)) to SH-SY5Y cells. From the MTT assay result, enhanced cell survival was observed with DL-NBP treatment, regardless of whether they are added before, simultaneously with or after the addition of H(2)O(2). For the in vivo experiment, Spontaneously Hypertensive rats and Wistar Kyoto control rats with chronic cerebral ischemia, which were induced by bilateral transection of the common carotid arteries, were given DL-NBP. Their performances in the place navigation test and spatial probe test in the Morris Water Maze have significantly improved compared with the DL-NBP untreated animals, indicating an improvement in spatial learning and memory in the ischemic-animals. In addition, in the chick embryonic chorioallantoic membrane assay, angiogenesis was more vigorous under the effects of DL-NBP, together with increased expression of growth factors, VEGF, VEGF-receptor and bFGF. All these suggested that one of the mechanisms of DL-NBP might be ameliorating vascular dementia and promoting angiogenesis.


Subject(s)
Benzofurans/therapeutic use , Dementia, Vascular/drug therapy , Drugs, Chinese Herbal , Neovascularization, Physiologic/drug effects , Neuroprotective Agents/therapeutic use , Animals , Benzofurans/pharmacology , Cell Line, Tumor , Chick Embryo , Dementia, Vascular/physiopathology , Humans , Immunohistochemistry , Male , Maze Learning , Neuroprotective Agents/pharmacology , Rats , Rats, Inbred SHR , Rats, Inbred WKY
20.
Microsc Res Tech ; 75(3): 258-64, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21809417

ABSTRACT

To study the deleterious effects of ketamine and the potential interaction effects between ethanol and ketamine on the cerebellum, functional magnetic resonance imaging (fMRI) tests were performed on the habitual ketamine users (n = 3) when they flexed and extended their upper limbs. Another fMRI test was performed on the same participants in which they consumed alcohol (12%, 200 mL) 1 h before the test. Downregulation on the activity of cerebellum was observed and the level of activation in the cerebellum decreased dramatically in habitual ketamine users with alcohol consumption before the test. Further studies were performed by using male ICR mice receiving treatment of ketamine only [30 mg kg(-1) intraperitoneally (i.p.)] or ethanol only everyday (0.5 mL 12% orally) and those with coadministration of the above dosages of ketamine and ethanol for 3 months. Fewer Purkinje cells were observed in the cerebellar sections of ketamine treated mice under silver staining. For TUNEL test, a significant increase in the apoptotic cells were observed in the cerebella of the ketamine treated mice (P = 0.016) and of those with co-administration of ketamine and ethanol (P < 0.001), when compared with the control. A statistical significance (P < 0.001) in two-way ANOVA test indicated that there might be an interactive mechanism between ethanol and ketamine acting on the cerebellum.


Subject(s)
Analgesics/adverse effects , Central Nervous System Depressants/adverse effects , Cerebellum/drug effects , Ethanol/adverse effects , Ketamine/adverse effects , Analgesics/administration & dosage , Animals , Apoptosis/drug effects , Central Nervous System Depressants/administration & dosage , Cerebellum/metabolism , Drug Interactions , Ethanol/administration & dosage , Humans , Image Interpretation, Computer-Assisted , In Situ Nick-End Labeling , Ketamine/administration & dosage , Magnetic Resonance Imaging , Male , Mice , Mice, Inbred ICR , Motor Activity/drug effects , Substance-Related Disorders/physiopathology
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