• Journal of Preventive Medicine and Public Health
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• 제51권1호
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• pp.1-5
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• 2018

Smokers keep smoking despite knowing that tobacco claims many lives, including their own and others'. What makes it hard for them to quit smoking nonetheless? Tobacco companies insist that smokers choose to smoke, according to their right to self-determination. Moreover, they insist that with motivation and willpower to quit smoking, smokers can easily stop smoking. Against this backdrop, this paper aims to discuss the addictive disease called tobacco use disorder, with an assessment of the addictiveness of tobacco and the reasons why smoking cessation is challenging, based on neuroscientific research. Nicotine that enters the body via smoking is rapidly transmitted to the central nervous system and causes various effects, including an arousal response. The changes in the nicotine receptors in the brain due to continuous smoking lead to addiction symptoms such as tolerance, craving, and withdrawal. Compared with other addictive substances, including alcohol and opioids, tobacco is more likely to cause dependence in smokers, and smokers are less likely to recover from their dependence. Moreover, the thinning of the cerebral cortex and the decrease in cognitive functions that occur with aging accelerate with smoking. Such changes occur in the structure and functions of the brain in proportion to the amount and period of smoking. In particular, abnormalities in the neural circuits that control cognition and decision-making cause loss of the ability to exert self-control and autonomy. This initiates nicotine dependence and the continuation of addictive behaviors. Therefore, smoking is considered to be a behavior that is repeated due to dependence on an addictive substance, nicotine, instead of one's choice by free will.

• 한국전문물리치료학회지
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• 제9권3호
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• pp.125-135
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• 2002

In most of the medical literature that discusses the common problem of movement in patients with cerebral lesions. This critical problem is ascribed to a mechanism involving uninhibited neural activity. The goals of neurological physical therapy are focus on reduce of muscle hypertonicity, facilitates muscle activities, and improve of performance in living environment. A variety of studies suggest that spasticity is a distinct problem and separate from the muscle weakness. It has become increasingly recognized that the major functional deficits following brain damage are largely due to negative features such as muscle weakness and loss of performance rather than spasticity. Adequate recruitment of prime mover, not release was able to carry out the movement tasks well. The strengthening exercise of spastic limbs on changes in muscle properties and performance skill, the repeated motor practice has been identified as crucial for motor recovery. This article support the concept that strengthening is an appropriate intervention to improve the quality of physical function in patients with central nervous system lesions. Further studies and therapeutic approaches should be efforts at improving motor neuron recruitment in agonist rather than reducing activity in antagonists while retraining muscle strengthening.

• Investigative Magnetic Resonance Imaging
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• 제23권4호
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• pp.390-394
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• 2019

Hemosiderosis is characterized by the deposition of excess iron in body tissues. The choroid plexus is an important part of the central nervous system that can be the primary site of iron overload. T2*-weighted gradient echo (GRE) sequence provides high sensitivity for demonstrating cerebral microhemorrhagic foci and iron deposition. In the present study, we describe the case of a 15-year-old boy with acute lymphoblastic leukemia, in whom repeated transfusion led to iron accumulation in the brain. GRE sequence effectively demonstrated hemosiderin deposition in the choroid plexus.

• Journal of Korean Neurosurgical Society
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• 제38권1호
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• pp.54-60
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• 2005

The clear cell meningioma[CCM] is a rare and recently described as a histologic variant of meningioma. It has been identified and included in new World Health Organization[WHO] classification of the Central Nervous System[CNS] tumors recently. The CCMs are histologically characterized by sheets of spindled to polygonal cells with clear cytoplasm, which is the expression of high glycogen concentration. The CCMs occur in younger patients and usually are located in the spinal canal and posterior fossa. The most interesting aspect of CCM is the high recurrence rate and aggressiveness. Poor outcome has been shown in intracranial and spinal tumor location, but the indicators that predict outcome have not been established. Until now 22 intracranial CCM cases had been reported in English literature and 3 cases in Korean. The authors report two cases of CCM located at cerebral convexity and one at cavernous sinus those were totally removed [Simpson Grade $I{\sim}II$] by subfrontal, frontal and orbitocranial approaches. The clinical, radiological, histopathological, and neurosurgical features of these cases are discussed with the relevant literatures.

• Archives of Pharmacal Research
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• 제29권4호
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• pp.265-275
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• 2006

In the developing brain, capillaries are differentiated and matured into the blood-brain barrier (BBB), which is composed of cerebral endothelial cells, astrocyte end-feet, and pericytes. Since the BBB regulates the homeostasis of central nervous system (CNS), the maintenance of the BBB is important for CNS function. The disruption of the BBB may result in many brain disorders including brain tumors. However, the molecular mechanism of BBB formation and maintenance is poorly understood. Here, we summarize recent advances in the role of oxygen tension and growth factors on BBB development and maintenance, and in BBB dysfunction related with brain tumors.

• 통합자연과학논문집
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• 제15권4호
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• pp.179-186
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• 2022

The c-Jun N-terminal kinase (JNK3) play major role in neurodegenerative diseases like Alzheimer's disease, Parkinson's disease, cerebral ischemia and other Central Nervous System disorders. Since JNK3 is primarily stated in the brain and stimulated by stress-stimuli, this situation is conceivable that inhibiting JNK3 could be a possible treatment for the mechanisms underlying neurodegenerative diseases. In this study drugs from Zinc15 database were screened to identify the JNK3 inhibitors by Molecular docking and Density functional theory approach. Molecular docking was done by Autodock vina and the ligands were selected based on the binding affinity. Our results identified top ten novel ligands as potential inhibitors against JNK3. Molecular docking revealed that Venetoclax, Fosaprepitant and Avapritinib exhibited better binding affinity and interacting with proposed binding site residues of JNK3. Density functional theory was used to compute the values for energy gap, lowest unoccupied molecular orbital (LUMO), and highest occupied molecular orbital (HOMO). The results of Density functional theory study showed that Venetoclax, Fosaprepitant and Avapritinib serves as a lead compound for the development of JNK3 small molecule inhibitors.

• 감성과학
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• 제26권3호
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• pp.149-160
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• 2023

본 연구에서는 뇌혈류 신호를 측정할 수 있는 시변자계 기반의 비접촉식 직물센서를 설계하여 뇌혈류 신호 검출 및 감성평가의 가능성을 탐색하고자 하였다. 직물센서는 40 denier의 은사를 30합사 한 후 컴퓨터 기계 자수하여 코일형 센서로 구현하였다. 뇌혈류 측정 실험을 위해 코일형 센서를 경동맥 부위에 부착하고, ECG (Electrocardiogram) 전극과 RSP (Respiration) 측정 벨트를 부착 및 착용하도록 하였으며, 동시에 초음파 진단기기를 사용해 도플러 초음파 검사(Doppler Ultrasonography)를 수행하여 혈류 속도를 측정하였다. 피험자에게 Meta Quest 2를 착용시키고, 실험을 위해 조작된 영상 시각 자극을 보여주면서 혈류 신호를 측정한 후 시각 자극에 대한 감성평가 설문지를 작성하도록 하였다. 측정 결과, 도플러 초음파 검사를 통해 측정된 혈류 속도 신호에 변화가 생길 때 직물센서로 측정한 신호도 함께 변화하는 것으로 나타났다. 이를 통해 코일형 직물센서를 이용하여 뇌혈류활동 신호를 측정할 수 있다는 것을 검증하였다. 또한, 감성평가를 위하여 ECG 신호와 PLL 신호(직물센서 신호)에서 추출한 HRV를 계산해서 비교한 결과, 시각 자극으로 인한 교감신경계와 부교감신경계의 활성화에 따른 비율의 변화에 대해서는 직물센서로 측정한 신호와 ECG 신호를 이용해 계산한 값이 비슷한 경향을 보이는 것으로 나타났다. 결론적으로, 본 연구에서 개발된 시변자계 기반의 코일형 직물 센서를 통해 뇌혈류 변화 측정 및 감성 모니터링이 가능할 것으로 사료된다.

• 대한유전성대사질환학회지
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• 제5권1호
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• pp.33-43
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• 2005

목적 : X 염색체 연관 부신백질이영양증은 과산화소체의 지방산 대사 장애로 인하여 포화 장쇄 지방산이 신경계의 수초와 부신 피질에 축적되어 여러 가지 신경학적 증상과 부신 기능 저하를 나타내는 드문 유전 질환이다. 증상의 발현 시기와 임상 경과에 따라 소아 대뇌형, 성인부신척수신경병형 등 여러 가지 형태로 나누어 지며 예후도 달라진다. 대상 및 방법 : 1996년 1월부터 2003년 6월까지 광주기독병원 소아과와 전남대병원 소아과에서 부신백질이영양증으로 진단받은 6명과 타병원에서 진단받고 골수 이식을 위해 내원한 7명, 총 13명의 남아들을 최소 1년 이상 추적 관찰하여 임상 경과를 분석하였다. 결과 : 1. 첫 신경학적 증상은 행동 장애, 청력 저하, 보행 장애, 시력 저하 및 사시 순이었고, 10명에서 ALD 가족력이 있었다. 2. 신경학적 증상의 발현시기, 증상의 진행 정도에 따라 분류하였을 때, 소아 대뇌형이 10명, 청소년 대뇌형이 2명, 신경학적 증상과 MRI 병변은 없이 부신 기능의 저하만 있는 "Addison-only"가 1명이었다. 1) 소아 대뇌형의 경우 8명이 사망하였는데 첫 증상 발현 시기는 평균 7.02세, 자연 경과로 첫 증상으로부터 식물 인간 상태에 이르는 기간은 1.35년, 사망에 이르는 기간은 3.35년으로 빠르게 진행하였다. Lorenzo oil을 투여하였던 2명에서 증상은 진행하였고, 제대혈 이식을 시행했던 2례는 질환의 진행과 이식편 대 숙주반응에 의해 사망하였다. 2) 청소년 대뇌형의 첫 증상 발현시기는 11.5세로, 2명 모두 현재 19세, 26세로 생존해 있으나, 1례는 식물 인간 상태이다. 3) "Addison only" 1례는 Lorenzo oil과 steroid를 투여하면서 3년째 증상 없이 지내고 있다. 3. 뇌 MRI에서 양측 두정엽과 후두엽의 백질을 침범한 형태가 대부분(11명)이었고, 청소년대뇌형 1명에서만 내포, 대뇌각과 뇌교를 침범하였다. 4. 진단 당시 부신 기능 저하가 67%에서 있었으며, ACTH만 상승된 형태였다. 결론 : 소아기에 발현한 부신백질이영양증의 경우, 두정엽과 후두엽 백질을 침범한 소아 대뇌형이 대부분이었고, 첫 증상 이후 빠르게 진행하여 사망에 이르는 치명적인 경과를 보였다. 따라서 가족력이 있는 경우, 많은 구성원에서 장쇄지방산 검사를 시행하여 조기에 무증상 환자를 진단하고 적극적으로 대처하는 것이 중요하리라 생각된다.

• Journal of Genetic Medicine
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• 제9권2호
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• pp.84-88
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• 2012

Purpose: Neurofibromatosis type 1 (NF1), which is caused by mutations of the NF1 gene, is the most frequent single gene disorder to affect the nervous system. Unidentified bright objects (UBOs) are commonly observed on brain magnetic resonance imaging (MRI) in patients with NF1. However, their clinical and pathologic significance is not well understood. The purpose of this study was to investigate the correlation between UBOs and cerebral glucose metabolism measured by $^{18}F$-2-Fluoro-2-deoxy-D-glucose ($^{18}F$-FDG) positron emission tomography (PET) in Korean patients with NF1. Materials and Methods: Medical records of 75 patients (34 males and 41 females) with NF1 who underwent brain MRI and PET between 2005 and 2011 were evaluated retrospectively. Clinical data including demographics, neurological symptoms, and brain MRI and PET findings, were reviewed. Results: UBOs were detected in the brain MRI scans of 31 patients (41%). The region most frequently affected by UBOs was the basal ganglia. The most frequent brain PET finding was thalamic glucose hypometabolism (45/75, 60%). Of the 31 patients with UBOs, 26 had thalamic glucose hypometabolism on brain PET, but the other 5 had normal brain PET findings. Conversely, of the 45 patients with thalamic glucose hypometabolism on brain PET, 26 showed UBOs on their brain MRI scans, but 19 had normal findings on brain MRI scans. Conclusion: UBOs on brain MRI scans and thalamic glucose hypometabolism on PET appear to be 2 distinctive features of NF1 rather than correlated symptoms. Because the clinical significance of these abnormal imaging findings remains unclear, a longitudinal follow-up study of changes in clinical manifestations and imaging findings is necessary.

• 대한장애인치과학회지
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• 제13권1호
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• pp.33-36
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• 2017

뇌성마비 환자들은 식이자세와 잇솔질에 대해 스스로 행동할 수 없기 때문에 의과적 치과적인 문제에 더 취약할 수 밖에 없다. 낮은 사회경제적 지위와 심각한 운동장애를 가진 뇌성마비 환자들은 특히 치과치료에서 소외되기 쉽다. 의과적 치료와 함께 구강관리는 뇌성마비 환자들의 삶의 질에 매우 중요한 관련이 있다. 그러므로, 장애인들의 삶의 질을 향상시키고 의료혜택으로부터 소외되지 않도록 정기적인 검진과 예방치료를 받기 위해서는 국가차원에서 공공의료서비스 및 시스템이 필요하다.