• 제목/요약/키워드: Korean medicine complex treatment

검색결과 810건 처리시간 0.027초

식품 단백질 유발성 장염 증후군: 임상적 접근과 병태생리의 최신 지견 (Food Protein-induced Enterocolitis Syndrome: an Update on Clinical Approaches and Its Pathophysiology)

  • 황진복
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제10권2호
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    • pp.117-128
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    • 2007
  • Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE mediated hypersensitivity disorder, which is associated with mainly gastrointestinal symptoms and has a delayed onset. The vomiting and/or diarrheal symptoms of FPIES typically begin in the first month of life in association with a failure to thrive, metabolic acidosis, and shock. Therefore, the differential diagnosis of FPIES and neonatal or infantile sepsis-like illnesses or gastroenteritis is difficult. The early recognition of indexes of suspicion for FPIES may help in the diagnosis and treatment of this disorder. The diagnosis of FPIES is generally made through clinical practice and food-specific IgE test findings are typically negative in this condition. Therefore, oral cow's milk challenge (OCC) remains the valid diagnostic standard for FPIES. An investigation of positive OCC outcomes helps to find out a diagnostic algorithm of criteria of a positive challenge in FPIES. Moreover, it has not been clearly determined in infantile FPIES when $1^{st}$ follow up-oral food challenge (FU-OFC) should be performed, with what kind of food protein (e.g., cow's milk, soy), and how much protein should be administered. Hence, to prevent the risk of inappropriate FU-OFC or accidental exposure and achieve appropriate dietary management, it is necessary to identify tolerance rates to major foods under the careful follow up of infantile FPIES patients. On the other hand, small intestinal enteropathy with villous atrophy is observed in FPIES and this enteropathy seems to be in part induced by both of epithelial apoptosis and intercellular junctional complex breakdown. The purpose of this report is to introduce an update on diagnostic and therapeutic approaches in FPIES and suggest the possible histopathological evidences in this disorder.

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The effect of five osteotropic factors on osteoprotegerin mRNA expression in gingival fibroblasts

  • Ko, Young-Kyung
    • Journal of Periodontal and Implant Science
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    • 제38권sup2호
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    • pp.395-404
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    • 2008
  • Purpose: Osteoprotegerin (OPG) is a secreted glycoprotein and a member of the tumor necrosis factor (TNF) receptor family that inhibits bone resorption by suppressing osteoclastogenesis. Gingival fibroblasts (GF) play a role in periodontal disease progression, and the purpose of this experiment was to evaluate influence of osteotropic factors on the expression of osteoprotegerin mRNA in these cells. Materials and Methods: In this experiment, the influence of osteoclastogenic factors, interleukin-1 beta (IL-$1{\beta}$), TNF-$\alpha$, prostanglandin E2 ($PEG_2$). parathyroid hormone (PTH) and 1$\alpha$, 25-dihydroxyvitamin $D_3$ on the expression of osteoprotegerin mRNA in GF was studied by Northern blot hybridization. Results: As expected, $PEG_2$ tended to inhibit OPG levels and this was most prominent at 24 hours of culture with $10^{-7}M$ of $PEG_2$. TNF-$\alpha$ at 10ng/ml and also at 25ng/ml decreased OPG levels to almost 30% of the control at 24 hours. This contrasts with reports of increased OPG levels from osteoblast/stromal cells and gingival fibroblasts stimulated by TNF-$\alpha$. Decrease of OPG levels with $PEG_2$ and TNF-$\alpha$ suggests a pathway whereby these mediators exert their resorptive effects. However, OPG levels were increased almost 3-fold at 24 hours with IL-1$\beta$(1 to 15ng/ml) and increased 1.4 fold with 24-hour treatment of $10^{-7}M$ PTH. Conclusion: Increase of OPG levels suggests that these 'osteoclastogenic' factors act in more complex ways and may act to inhibit bone resorption in inflammatory periodontitis. This result supports the role of OPG as a negative feedback mechanism in osteoclastic activity.

Agreement between cone-beam computed tomography and functional endoscopic sinus surgery for detection of pathologies and anatomical variations of the paranasal sinuses in chronic rhinosinusitis patients: A prospective study

  • Nikkerdar, Nafiseh;Eivazi, Nastaran;Lotfi, Mohana;Golshah, Amin
    • Imaging Science in Dentistry
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    • 제50권4호
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    • pp.299-307
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    • 2020
  • Purpose: The diagnosis of chronic rhinosinusitis requires a comprehensive knowledge of the signs and symptoms of the disease and an accurate radiographic assessment. Computed tomography (CT) is the superior imaging modality for diagnosis of chronic rhinosinusitis. However, considering the lower dose and higher resolution of cone-beam computed tomography (CBCT) compared to CT, this study aimed to assess the agreement between the findings of CBCT and functional endoscopic sinus surgery (FESS). Materials and Methods: This descriptive prospective study evaluated 49 patients with treatment-resistant chronic rhinosinusitis who were candidates for FESS. Preoperative CBCT scans were obtained before patients underwent FESS. The agreement between the CBCT findings and those of FESS was determined using the kappa correlation coefficient. The frequency of anatomical variations of the paranasal sinuses was also evaluated on CBCT scans. Results: Significant agreement existed between pathological findings on CBCT scans and those of FESS, such that the kappa correlation coefficient was 1 for mucosal thickening, 0.644 for nasal deviation, 0.750 for concha bullosa, 0.918 for nasal polyp, 0.935 for ostiomeatal complex (OMC) obstruction, and 0.552 for infundibulum thickening. Furthermore, 95.9% of patients had 1 or more and 79.6% had 2 or more anatomical variations, of which nasal deviation was the most common (67.3%). Conclusion: Considering the significant agreement between the findings of CBCT and FESS for the detection of pathological changes in the paranasal sinuses, CBCT can be used prior to FESS to detect chronic rhinosinusitis and to assess anatomical variations of the OMC.

Low lysine stimulates adipogenesis through ZFP423 upregulation in bovine stromal vascular cells

  • Joseph F., dela Cruz;Kevin Wayne Martinez, Pacunla;Seong Gu, Hwang
    • Journal of Animal Science and Technology
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    • 제64권6호
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    • pp.1173-1183
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    • 2022
  • Adipogenesis is a complex process comprising commitment and a differentiation stages. Through research, many different transcriptional factors were found to mediate preadipocyte commitment and differentiation. Lysine has a potential of regulating the commitment and differentiation of preadipocytes. In the present study, intramuscular stromal vascular cells (SVC) isolated from Hanwoo beef cattle were used to elucidate the effects of low lysine level on adipogenesis. SVC were isolated and incubated with various concentrations of lysine (0, 37.5, 75, 150 and 300 µg/mL). No significant difference were observed in the proliferation of SVC after 24 and 48 h of incubation with different concentration of lysine. On preadipocyte determination, reducing the level of lysine significantly increased the expression of preadipocyte commitment gene Zinc finger protein 423 and Preadipocyte factor-1. Upon differentiation, Oil Red O staining revealed that lipid accumulation and triglyceride content significantly increased with the decreasing lysine levels in the media. Expression levels of peroxisome proliferator-activated receptor-γ, CCAAT enhancer binding protein-α, sterol regulatory element binding protein-1c, Fatty Acid Binding Protein 4 and stearoyl CoA desaturase were upregulated by the decreased level of lysine. These data suggest the potential mechanism of action for the improved preadipocyte commitment and adipocyte differentiation in bovine intramuscular SVC upon treatment with low levels of lysine. These findings may be valuable in developing feed rations that promote deposition of intramuscular fat in beef cattle through lysine level modification.

Efficient Generation of Dopaminergic Neurons from Mouse Ventral Midbrain Astrocytes

  • Jin Yi Han;Eun-Hye Lee;Sang-Mi Kim;Chang-Hwan Park
    • Biomolecules & Therapeutics
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    • 제31권3호
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    • pp.264-275
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    • 2023
  • Parkinson's disease (PD) is a common neurodegenerative disorder characterized by tremors, bradykinesia, and rigidity. PD is caused by loss of dopaminergic (DA) neurons in the midbrain substantia nigra (SN) and therefore, replenishment of DA neurons via stem cell-based therapy is a potential treatment option. Astrocytes are the most abundant non-neuronal cells in the central nervous system and are promising candidates for reprogramming into neuronal cells because they share a common origin with neurons. The ability of neural progenitor cells (NPCs) to proliferate and differentiate may overcome the limitations of the reduced viability and function of transplanted cells after cell replacement therapy. Achaete-scute complex homolog-like 1 (Ascl1) is a well-known neuronal-specific factor that induces various cell types such as human and mouse astrocytes and fibroblasts to differentiate into neurons. Nurr1 is involved in the differentiation and maintenance of DA neurons, and decreased Nurr1 expression is known to be a major risk factor for PD. Previous studies have shown that direct conversion of astrocytes into DA neurons and NPCs can be induced by overexpression of Ascl1 and Nurr1 and additional transcription factors genes such as superoxide dismutase 1 and SRY-box 2. Here, we demonstrate that astrocytes isolated from the ventral midbrain, the origin of SN DA neurons, can be effectively converted into DA neurons and NPCs with enhanced viability. In addition, when these NPCs are inducted to differentiate, they exhibit key characteristics of DA neurons. Thus, direct conversion of midbrain astrocytes is a possible cell therapy strategy to treat neurodegenerative diseases.

간 0형 당원축적병의 임상 표현형과 식사관리 (Clinical Phenotypes and Dietary Management of Hepatic Glycogen Storage Disease Type 0)

  • 신영림
    • 대한유전성대사질환학회지
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    • 제23권2호
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    • pp.8-14
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    • 2023
  • 간 당원축적병 0형은 glycogen synthase 2 유전자에 부호화되어 있는 간 당원 합성효소의 결핍으로 비정상적으로 당원 생성이 되는 상염색체 열성 유전 질환이다. 당원축적병 0형의 임상 양상은 공복시에 고케톤혈증 저혈당증을 나타내고 식사후 고혈당과 고젖산혈증을 보인다. 당원축적병 0형은 현재까지 적은 수만 보고되었는데 증상이 경하거나 심한 저혈당이 드물고 또는 무증상이거나 나이가 듦에 따라 점차 증상이 사라지는 양상을 보이기 때문에 진단을 놓치는 경우가 있을 것으로 생각된다. 필수적 치료 전략은 포도당신생성을 자극하기 위해 고단백 식사, 낮동안 저혈당을 방지하기 위해서 잦은 식사 횟수, 밤 동안 천천히 포도당을 방출하기 위해 생옥수수전분가루 같은 복합 탄수화물을 먹는 것이다. 당원축적병 0형은 예후는 좋고 적절한 치료를 하면 정상적으로 성장하며 합병증도 발생하지 않는다. 성인이 될수록 심한 저혈당은 보이지 않게 되지만 지속적인 식사 관리는 필요하다.

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Bell's palsy after concomitant chemoradiotherapy: a case report and literature review

  • Sul Gi Choi;Ji Seok Oh;Hoon Myoung;Mi Hyun Seo
    • Journal of Dental Anesthesia and Pain Medicine
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    • 제24권2호
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    • pp.129-135
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    • 2024
  • Concomitant chemoradiotherapy (CCRT) treated patients experience various complications. We present a rare case of post-CCRT Bell's palsy and describe its various possible causes, so as to increase awareness among clinicians about Bell's palsy being a CCRT-associated adverse effect. The patient was a 48-year-old man diagnosed with squamous cell carcinoma who presented with post-CCRT Bell's palsy. After radiotherapy for 6 weeks (overall 67.5 Gy) and four rounds of cisplatin chemotherapy, he complained of paralysis of the entire left face. A test was performed 33 days after the last CCRT session to differentiate Bell's palsy from other causative factors. Based on magnetic resonance imaging findings, facial nerve invasion due to tumor size increase was determined to not cause Bell's palsy. Inflammation of the left Eustachian tube was observed. Hence, steroids and famciclovir were administered, which markedly improved the facial paralysis symptoms within 56 days after facial paralysis development. In conclusion, patients can develop Bell's palsy owing to complex effects of various CCRT mechanisms. Although the exact cause of Bell's palsy has not been identified and the effectiveness of drug treatment was questionable in this case, unlikely causative factors should be excluded through various tests and appropriate and timely measures must be adopted.

용적변조회전 방사선치료에서 선량전달의 중단 및 재시작에 따른 정확성 평가 (The Accuracy Evaluation according to Dose Delivery Interruption and Restart for Volumetric Modulated Arc Therapy)

  • 이동형;배선명;곽정원;강태영;백금문
    • 대한방사선치료학회지
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    • 제25권1호
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    • pp.77-85
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    • 2013
  • 목 적: 용적변조회전 방사선치료는 겐트리 회전과 다엽콜리메이터, 선량률이 연동되어 진행되며 치료 중 선량 전달의 중단이 발생한 경우 겐트리와 다엽콜리메이터가 최초위치부터 다시 동작하여 정지된 지점부터 선량전달이 재개된다. 본 연구는 용적 변조회전 방사선치료의 치료 중단과 재 진행에 따른 선량전달의 오차를 분석하고자 하였다. 대상 및 방법: 10명의 환자를 대상으로 전산화치료계획시스템(Eclipse V10.0, Varian, USA)을 이용하여 용적변조회전 방사선 치료 계획을 수립하였다. TRILOGY (Varian, USA)의 6 MV 선속을 이용하여 계획된 선량을 이차원 배열 검출기와 CUBE (IBA dosimetry, Germany)팬텀에 조사하였다. OmniPro I'mRT system (V1.7b, IBA dosimetry, Germany)을 통해 4회에 걸쳐 일반적인 선량전달의 일관성을 평가 하고 선량 전달의 중단 또는 도어 인터락 발생으로 인해 선량 전달이 중단되고 최초지점부터 다시 시작되어 조사되는 경우와 비교하여 감마지수(Gamma index)의 변화를 분석하였다. 결 과: 선량 전달이 정상적으로 이루어진 경우에 각각의 감마 평균 신호 값의 차이는 0.1로 나타났고, 선량 전달의 중단이 발생한 경우 0.128로 나타났으며 도어 인터락의 경우 0.141로 나타났다. 각각의 경우 감마 표준편차 값의 차이는 0.071, 0.091, 0.099로 나타났고, 감마 최대값의 차이는 0.286, 0.379, 0.413으로 나타났다. Gamma pass rate (3%, 3 mm)는 허용 오차 범위를 만족하였고, T검증 결과 95% 신뢰구간에서 P-value가 0.05 미만으로 유의한 차이를 보였다. 결 론: 본 실험에서 치료 중 선량 전달의 중단 및 재시작에 관한 정확성을 평가해 본 결과 통계적으로는 차이가 있으나 임상적으로 허용 오차 범위이내로 문제가 없다는 것을 알 수 있었다. 그러나 겐트리와 다엽콜리메이터, 선량률의 연동으로 정확성이 요구되는 치료방법인 만큼 선량적인 측면에서 치료 중단에 따른 차이는 간과할 수 없다. 그러므로 갑작스러운 치료 중단 상황이 발생한 경우 추가적인 정도관리 절차를 통해 정확한 선량평가가 이루어져야 할 것으로 사료된다.

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향어에서의 oxolinic acid 흡수와 배설속도 (The absorption and excretion times of carp, Cyprinus carpio, treatment with oxolinic acid)

  • 정현도;하재이;허민도;정준기
    • 한국어병학회지
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    • 제5권2호
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    • pp.135-142
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    • 1992
  • 새로운 수산용 항생제로서 사용이 증가되고 있는 OX의 흡수 및 배설속도를 측정하고 수온, 급이등의 외적 환경이 이들 속도에 미치는 영향을 평가하였다. 동시에 OTC에 대비한 OX의 항균성 그리고 어류 혈장내 단백질과의 결합도 비교검토하였다. OX는 조사된 13균주중 11균주에 대해 OTC보다 10배이하의 낮은 MIC치를 보였고 향어나 틸라피아의 혈장내 단백질과의 complex 형성에 의한 역가 감소도 OTC에 비교해서 나타나지 않아 일반적인 세균성어병의 치료제로서 OTC 보다 우수한 것으로 나타났다. 향어에의 OX 투여를 경구, 근육주사, 정맥주사, 약욕등의 방법으로 실시하여 혈중 농도를 비교 측정하였을 때, i.v와 약욕법은 높은 초기 혈중 농도와 빠른 배설 속도를 보였다. 경구 투여와 근육 주사시는 24~28시간 후 최고 혈중 농도에 도달하고 이후 천천히 배설되었으며, 특히 i.m 투여에서의 OX bioavailability는 경구 투여보다 높게 나타났다. 이러한 약동력학적인 특성은 수온이 $30^{\circ}C$$20^{\circ}C$에서 차이를 보이지 않았으나 2주일 절식을 시킨 향어에 약욕방법으로 항생제 투여를 하면 절식어에서의 초기 혈중 농도가 정상급이어에 비해 훨씬 낮게 나타나 어류 표피나 아가미의 생리 활성도에 따른 항생제의 흡수율 변화를 추정케 해 주었다.

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갈색거저리 유충에서 추출한 펩타이드의 항산화 특성 (Antioxidant Properties of Peptides Extracted from Tenebrio molitor Larvae)

  • 김삼웅;갈상완;지원재;방우영;박소정;김태완;방규호
    • 생명과학회지
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    • 제33권5호
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    • pp.383-390
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    • 2023
  • 본 연구는 기능성 식품의 개발을 위해 갈색거저리 유충 유래 추출물에서 새로운 생리활성 펩타이드를 확인하는 것이다. 동결건조된 T. molitor 유충에서 다양한 용매로 시간에 따라 추출하였다. T. molitor 유충 추출 결과 물 추출물에서 5시간과 10시간에서 총 단백질과 고형분 함량당 각각 가장 높은 2,2,1-diphenyl-1-picrylhydrazyl (DPPH) 활성을 보였다. 물 추출물을 메탄올 농도에 따라 분획하였을 때, 높은 메탄올 농도는 상등액 중에 고분자량 단백질의 수준을 감소시키는 반면, 상등액의 DPPH 활성 수준을 증가시켜 저분자량 펩타이드가 항산화 활성을 매개하는 것으로 나타났다. 유기용매 분배에서 부탄올을 제외한 유기 용매 분배에서 물층에서 유사한 활성을 보였다. 유기용매분획물을 열처리 후 활성이 28~44% 감소하여 열에 대한 불안정한 성분이 존재하는 것으로 추정되었다. 물 추출물에 프로테아제 K를 첨가하면 DPPH 활성이 10~20% 증가하여 전체 단백질에서 방출되는 펩타이드가 항산화 활성을 부분적으로 증가시켰음을 알 수 있다. 그러므로, T. molitor 유충 추출물은 항산화제로써 기능을 수행할 수 있는 물질이 존재하는 것으로 제의할 수 있다.