1.Compensation for Occupational Neurological and Mental Disorders.
Journal of Korean Medical Science 2014;29(Suppl):S59-S65
Standards for the recognition of occupational diseases (ODs) in Korea were established in 1954 and have been amended several times. In 2013, there was a significant change in these standards. On the basis of scientific evidence and causality, the International Labour Organization list, European Commission schedule, and compensated cases in Korea were reviewed to revise the previous standards for the recognition of ODs in Korea. A disease-based approach using the International Classification of Diseases (10th version) was added on the previous standards, which were agent-specific approaches. The amended compensable occupational neurological disorders and occupational mental disorders (OMDs) in Korea are acute and chronic central nervous system (CNS) disorders, toxic neuropathy, peripheral neuropathy, manganese-related disorders, and post-traumatic stress disorder. Several agents including trichloroethylene (TCE), benzene, vinyl chloride, organotin, methyl bromide, and carbon monoxide (CO) were newly included as acute CNS disorders. TCE, lead, and mercury were newly included as chronic CNS disorders. Mercury, TCE, methyl n-butyl ketone, acrylamide, and arsenic were newly included in peripheral neuropathy. Post-traumatic stress disorders were newly included as the first OMD. This amendment makes the standard more comprehensive and practical. However, this amendment does not perfectly reflect the recent scientific progress and social concerns. Ongoing effort, research, and expert consensus are needed to improve the standard.
Female
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Humans
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Mental Disorders/chemically induced/*economics/pathology
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Nervous System Diseases/chemically induced/*economics/pathology
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Occupational Diseases/*economics
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Occupational Exposure
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Republic of Korea
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Stress Disorders, Post-Traumatic/diagnosis/*economics
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Workers' Compensation/*economics
2.A reviewing for abusing of ketamine.
Journal of Forensic Medicine 2007;23(4):312-315
Ketamine is a noncompetitive NMDA receptor antagonist and comes into being a new problem of drug abuse. It can cause a certain extent of hallucination, which makes ketamine be abused in the casinos. The paper reviews the pharmacological and toxicology characteristic of Ketamine, the possible physiological mechanism and the methods for detecting Ketamine abuse.
Anesthetics, Dissociative/toxicity*
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Cerebral Cortex/drug effects*
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Humans
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Illicit Drugs
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Ketamine/toxicity*
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Mental Disorders/chemically induced*
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Receptors, Dopamine/drug effects*
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Receptors, N-Methyl-D-Aspartate/drug effects*
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Substance Abuse Detection/methods*
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Substance-Related Disorders/prevention & control*
3.Advances in research of ketamine addiction mechanism.
Wei-Li LIU ; Shi-Zhong BIAN ; Zhen-Lun GU ; Xiao-Gang JIANG ; Zheng-Hong QIN
Journal of Forensic Medicine 2009;25(3):200-207
Ketamine is a phencyclidine derivative acting primarily as a noncompetitive antagonist of N-methyl-D-aspartate (NMDA) excitatory glutamate receptors. As a common intravenous anaesthetic in clinic, it is also increasingly abused because of its hallucination and addiction effects. Based on the pharmacological and toxicologic characteristics of ketamine and the acknowledged addiction mechanism of other abused drugs, this article reviews the possible addiction mechanism of the ketamine in the aspects of its enhanced effects and reward systems, the anatomic structures, the related receptors and the individual differences.
Anesthetics, Dissociative/adverse effects*
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Animals
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Brain/drug effects*
;
Humans
;
Illicit Drugs
;
Ketamine/adverse effects*
;
Mental Disorders/chemically induced*
;
Rats
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Receptors, Dopamine/drug effects*
;
Receptors, N-Methyl-D-Aspartate/drug effects*
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Substance-Related Disorders
4.Levels of oxidative stress parameters and the protective effects of melatonin in psychosis model rat testis.
Bekir S PARLAKTAS ; Birsen OZYURT ; Huseyin OZYURT ; Ayten T TUNC ; Ali AKBAS
Asian Journal of Andrology 2008;10(2):259-265
AIMTo evaluate the effects of melatonin on antioxidant enzyme levels and histopathologic changes in dizocilpine (MK-801)-induced psychosis model rat testis.
METHODSA total of 24 adult male Wistar-Albino rats were divided into three groups with 8 in each. Group I was used as control. Rats in Group II were injected with MK-801 (0.5 mg/kg body weight i.p. for 5 days). In addition to MK-801, melatonin (50 mg/kg body weight i.p. once a day for 5 days) was injected into the rats in Group III. The testes were harvested bilaterally for biochemical and histopathological examinations. Antioxidant enzyme activities, malondialdehyde, protein carbonyl and nitric oxide (NO) levels in testicular tissues were analyzed using spectrophotometric analysis methods. Histopathological examinations of the testes were also performed.
RESULTSMK-801 induced testicular damage, which resulted in significant oxidative stress (OS) by increasing the levels of antioxidant enzymes. The malondialdehyde, protein carbonyl and NO levels were increased in testicular tissues of rats. Treatment with melatonin led to significant decrease in oxidative injury. Administration of melatonin also reduced the detrimental histopathologic effects caused by MK-801.
CONCLUSIONThe results of the present study showed that MK-801 cause OS in testicular tissues of rats and treatment with melatonin can reduce the harmful effects of MK-801.
Animals ; Antioxidants ; pharmacology ; Disease Models, Animal ; Dizocilpine Maleate ; adverse effects ; pharmacology ; Male ; Malondialdehyde ; Melatonin ; pharmacology ; Mental Disorders ; chemically induced ; Nitric Oxide ; Oxidative Stress ; drug effects ; Protein Carbonylation ; Psychotropic Drugs ; adverse effects ; pharmacology ; Rats ; Rats, Wistar ; Testis ; drug effects ; enzymology ; pathology