240 research outputs found

    Association between thyroid hormones and the components of metabolic syndrome

    Get PDF
    BACKGROUND: Thyroid hormones are known to have direct and indirect effects on metabolism. Individuals with metabolic syndrome, a disease that is growing in incidence at a rapid rate, are at higher risk for cardiovascular disease, diabetes, and cancer. The aim of this study was to identify whether significant correlations exist between thyroid hormone levels and components of the metabolic syndrome in the general population of Korea. METHODS: The data were collected from the sixth Korea National Health and Nutrition Examination Surveys from 2013 to 2015. A total of 1423 participants were tested for thyroid function. The analysis of variance and multiple linear regression were performed to analyze the relationship between thyroid hormone level and components of the metabolic syndrome. RESULTS: A positive association between free thyroxine and fasting glucose level was observed in patients with high free thyroxine levels (>/=1.70 ng/dL, beta = 15.992, p = < 0.0001), when compared with patients with normal-middle free thyroxine levels. Moreover, a negative association was observed between free thyroxine and triglyceride levels in patients with normal-high free thyroxine levels (beta = - 21.145, p = 0.0054) and those with high free thyroxine levels (beta = - 49.713, p = 0.0404). CONCLUSION: Free thyroxine shows a partially positive association with fasting glucose and a partially negative association with triglycerides in the Korean population. In patients with abnormal thyroid function, follow up tests for glucose levels and lipid profiling during treatment for thyroid dysfunction would be beneficial in terms of overlooking metabolic syndrome and to prevent related diseases.ope

    A Case of Sarcoidosis Combined with Massive Ascites

    Get PDF
    Sarcoidosis is a multi-systemic granulomatous disease of unknown cause, which most commonly involves lung, skin, eye, liver and lymph nodes. Herein, we report a case of sarcoidosis presented with massive ascites. A 47-year-old male patient visited our hospital with symptoms of general weakness and weight loss from past 4 months. Abdomen computed tomography showed multiple lymphadenopathy and hepatosplenomegaly. Lymph node biopsy demonstrated non-caseating granulomas. After biopsy, development of massive uncontrolled ascites was noted. Liver biopsy showed non-cirrhotic hepatic and portal fibrosis and omental biopsy showed submesothelial diffuse fibrosis and focal chronic inflammation, which were suggestive of hepatic and peritoneal involvement in sarcoidosis. Ascites was controlled after subsequent treatment with corticosteroids and methotrexate.ope

    Tolerability and Effectiveness of Switching to Dulaglutide in Patients With Type 2 Diabetes Inadequately Controlled With Insulin Therapy

    Get PDF
    Aims: Glucagon-like peptide 1 (GLP-1) receptor agonists have demonstrated strong glycemic control. However, few studies have investigated the effects of switching from insulin to GLP-1 receptor agonists. We aimed to investigate, using real-world data, whether switching to dulaglutide improves glycemic control in patients with type 2 diabetes mellitus (T2D) inadequately controlled with conventional insulin treatment. Materials and methods: We retrospectively evaluated 138 patients with T2D who were switched from insulin to dulaglutide therapy. We excluded 20 patients who dropped out during the follow-up period. The participants were divided into two groups according to whether they resumed insulin treatment at 6 months after switching to a GLP-1 receptor agonist (group I) or not (group II). A multiple logistic regression analysis was performed to evaluate the parameters associated with the risk of resuming insulin after replacement with dulaglutide. Results: Of 118 patients initiated on the GLP-1 receptor agonist, 62 (53%) resumed insulin treatment (group I), and 53 (47%) continued with GLP-1 receptor agonists or switched to oral anti-hypoglycemic agents (group II). Older age, a higher insulin dose, and lower postprandial glucose levels while switching to the GLP-1 receptor agonist were associated with failure to switch to the GLP-1 receptor agonist from insulin. Conclusions: A considerable proportion of patients with T2D inadequately controlled with insulin treatment successfully switched to the GLP-1 receptor agonist. Younger age, a lower dose of insulin, and a higher baseline postprandial glucose level may be significant predictors of successful switching from insulin to GLP-1 receptor agonist therapy.ope

    ์„ฑ์žฅํ˜ธ๋ฅด๋ชฌ ๋ถ„๋น„ ๋‡Œํ•˜์ˆ˜์ฒด ์ข…์–‘์˜ ์ˆ˜์ˆ ์  ์™„์น˜ ํ›„ ๋ฐœ๊ฒฌ๋œ ์ง€์—ฐํ˜• ์ž๊ฐ€๋ฉด์—ญ ๋‹น๋‡จ๋ณ‘ 1์˜ˆ

    Get PDF
    Acromegaly is generally caused by a benign growth hormone (GH)-secreting pituitary adenoma. It is characterized by a wide range of complications; cardiovascular, respiratory, bone and joint, and metabolic complications. Among them, impaired glucose tolerance and diabetes mellitus, due to GH-induced insulin resistance, has been reported in approximately 16-46% and 19-56%. They are usually improved following the treatment of acromegaly, surgical or medical therapy. We report a first case of 36-year-old man who was paradoxically diagnosed with GAD antibody positive latent autoimmune diabetes in adults (LADA) after the surgical cure of acromegaly.ope

    A 47,X,+t(X;X)(p22.3;p22.3)del(X)(p11.23q11.2),Y Klinefelter Variant with Morbid Obesity

    Get PDF
    Klinefelter syndrome is the most common type of genetic cause of hypogonadism. This syndrome is characterized by the presence of 1 or more extra X chromosomes. Phenotype manifestations of this syndrome are small testes, fibrosis of the seminiferous tubules, inability to produce sperm, gynecomastia, tall stature, decrease of serum testosterone and increases of luteinizing hormone and follicle stimulating hormone. Most patients with Klinefelter syndrome are tall, with slender body compositions, and reports of obesity are rare. We report the case of a 35-yr-old man with hypogonadism and morbid obesity and diabetes mellitus. He had gynecomastia, small testes and penis, very sparse body hair and his body mass index was 44.85. He did not report experiencing broken voice and was able to have erections. We conducted a chromosome study. His genotype was 47,X,+t(X;X)(p22.3;p22.3)del(X)(p11.23q11.2). In this case, the patient was diagnosed as Klinefelter syndrome. He showed rare phenotypes like morbid obesity and average height and the phenotype may be caused by the karyotype and the excess number of X chromosome. Further studies of the relationship between chromosomes and phenotype are warranted.ope

    Duodenal adenocarcinoma following a neuroendocrine tumor in the duodenum

    Get PDF
    Primary duodenal adenocarcinoma is a rare malignant neoplasm accounting for 0.3% of all gastrointestinal tract carcinomas. We herein present one case of duodenal adenocarcinoma after duodenal neuroendocrine carcinoma. Poorly differentiated duodenal neuroendocrine carcinoma with liver metastasis (TxNxM1) was confirmed, and eight cycles of palliative chemotherapy (5-fluorouracil/etoposide/cisplatin) were administered. The patient was then in a clinically complete response status. About 1 year later, newly developed adenocarcinoma was detected at the same site. It was completely surgically resected, and the patient was cured.ope

    ้ซ”็ณป็š„ ๅฑ้šช์˜ ํ˜„์‹ค์  ์ ‘๊ทผ๋ฒ•๊ณผ ์ด๋ฅผ ์ด์šฉํ•œ ์„ฑ๊ณผ์ธก์ •

    No full text
    1980-03ไผๆฅญ่ฒกๅ‹™์˜ ็›ฎๆจ™๋Š” ไผๆฅญ์˜ ๅƒนๅ€ค๋ฅผ ๆœ€ๅคงๅŒ–ํ•จ์œผ๋กœ์จ ๆ ชไธป์˜ ๅฏŒ๋ฅผ ๆฅตๅคงๅŒ–์‹œํ‚ค๋Š” ๊ฒƒ์ด๋‹ค. ๊ทธ๋Ÿฌ๋‚˜ ไผๆฅญ์ด ๅƒนๅ€ค่ฟฝๆฑ‚๋ฅผ ์œ„ํ•˜์—ฌ ๆŠ•่ณ‡ๆฑบๅฎš์„ ํ•  ๋•Œ๋Š” ํ•ญ์ƒ ๆœŸๅพ…๋˜๋Š” ๆŠ•่ณ‡ๆ”ถ็›Š๊ณผ ๋”๋ถˆ์–ด ๅฑ้šช์ด ๋”ฐ๋ฅด๊ธฐ ๋งˆ๋ จ์ด๋‹ค. ๅฑ้šช์ด ์–ด๋–ค ๆ„ๅ‘ณ๋ฅผ ๊ฐ€์ง€๊ณ  ์žˆ๋Š๋ƒ ํ•˜๋Š” ๊ฒƒ์— ๊ด€ํ•˜์—ฌ๋Š” ๋‹ค์†Œ ่ฆ‹่งฃ์˜ ์ฐจ์ด๋Š” ์žˆ์œผ๋‚˜, ์ ์–ด๋„ ๅฑ้šช์€ ๆœชไพ†่ฑซๆธฌ์— ๋Œ€ํ•œ ไธๅฎŒๅ…จๆ€ง์—์„œ ์˜ค๋Š” ๊ฒƒ์œผ๋กœ ไธ็ขบๅฏฆๆ€ง์— ๊ธฐ์ธํ•œ๋‹ค๊ณ  ๋ณผ ์ˆ˜ ์žˆ๋‹ค. ๆŠ•่ณ‡ๅฎถ์˜ ๅฑ้šช์€ ๆœชไพ†์˜ ็พ้‡‘ํ๋ฆ„์ด๋‚˜ ๊ฐ€๋Šฅํ•œ ๆ”ถ็›Š์˜ ๅˆ†ๆ•ฃ็จ‹ๅบฆ(variability of possible return)๋ฅผ ๋งํ•˜๋ฉฐ, ๆœชไพ†์— ๋Œ€ํ•œ ไธ็ขบๅฏฆ๋กœ ์ธํ•˜์—ฌ ๅฏ่ƒฝํ•œ ๆ”ถ็›Š์ด ๅนณๅ‡ๅ€ค์— ์„œ ์ดํƒˆํ•˜๋Š” ์ •๋„๋ฅผ ๋งํ•œ๋‹ค

    (The) effect of nano-sized carbonate apatite on remineralization of artificial caries-like lesions

    No full text
    ์น˜์˜ํ•™๊ณผ/๋ฐ•์‚ฌ[ํ•œ๊ธ€] ์น˜์•„์šฐ์‹์ฆ์€ ๋ฌด๊ธฐ์งˆ ์šฉํ•ด์™€ ์œ ๊ธฐ์งˆ ํŒŒ๊ดด๋กœ ์น˜์•„์†์ƒ์ด ์ผ์–ด๋‚˜๋Š” ๊ตฌ๊ฐ•์˜์—ญ์—์„œ ๋‚˜ํƒ€๋‚˜๋Š” ๊ฐ€์žฅ ๋Œ€ํ‘œ์ ์ธ ์งˆํ™˜์œผ๋กœ ๋ฌด๊ธฐ์งˆ ๊ตํ™˜์˜ ํ‰ํ˜•์„ ์œ ์ง€์‹œ์ผœ ์ค€๋‹ค๋ฉด ํƒˆํšŒ๋ฅผ ๋ฐฉ์ง€ํ•˜์—ฌ ์น˜์•„์šฐ์‹์ฆ์„ ์˜ˆ๋ฐฉํ•  ์ˆ˜ ์žˆ์œผ๋ฉฐ ์น˜์•„๋ฅผ ๊ฑด๊ฐ•ํ•˜๊ฒŒ ์œ ์ง€ํ•  ์ˆ˜ ์žˆ๋‹ค. ๋ณธ ์—ฐ๊ตฌ๋Š” ์ดˆ๊ธฐ ๋ฒ•๋ž‘์งˆ ์šฐ์‹์˜ ํšŒ๋ณต๊ณผ ์น˜์•„์˜ ์žฌ๊ด‘ํ™”๋ฅผ ์œ ๋„ํ•˜๊ธฐ ์œ„ํ•˜์—ฌ ์ธ๊ณต ์ดˆ๊ธฐ ์šฐ์‹๋ณ‘์†Œ๋ฅผ ํ˜•์„ฑํ•œ ๋ฒ•๋ž‘์งˆ์— nano-sized Carbonate Apatite(n-CAP)์˜ ์žฌ๊ด‘ํ™” ํšจ๊ณผ๋ฅผ Casein Phosphopeptide Amorphous-Calcium Phosphate(CPP-ACP)์™€ ์ƒํ˜ธ ๋น„๊ตํ•˜์—ฌ ๋ถ„์„ํ•˜์˜€๋‹ค. n-CAP์˜ ๋†๋„๋Š” 0%, 5%, 10%๋กœ ๊ตฌ๋ถ„ํ•˜์˜€์œผ๋ฉฐ CPP-ACP๋Š” 10% ํ•จ์œ ๋˜์–ด ์‹œํŒ๋˜๊ณ  ์žˆ๋Š” Tooth MousseTM ๋ฅผ pH ์ˆœํ™˜๋ชจ๋ธ์„ ์ด์šฉํ•˜์—ฌ 14์ผ๊ฐ„ ๊ฐ๊ฐ ํ•˜๋ฃจ 3ํšŒ์”ฉ 5๋ถ„๊ฐ„ ์ฒ˜๋ฆฌํ•˜์˜€์œผ๋ฉฐ ์ฒ˜๋ฆฌ ์ „, ํ›„์˜ ํ‘œ๋ฉด์˜ ๊ฒฝ๋„ ๋ณ€ํ™”๋ฅผ Vickers Hardness Number (VHN)๋กœ ํ‰๊ฐ€ํ•˜์˜€๊ณ  Knoop Hardness number (KHN)๋กœ ๋ฌด๊ธฐ์งˆ์˜ ์†Œ์‹ค์ •๋„(vol %)๋ฅผ ?Z ๊ฐ’์œผ๋กœ ์ธก์ •ํ•˜์—ฌ ๋ณ‘์†Œ ์‹ฌ๋ถ€๋กœ์˜ ์žฌ๊ด‘ํ™”์— ๋ฏธ์นœ ์˜ํ–ฅ์„ ์‚ดํŽด๋ณด์•˜๋‹ค. ๋˜ํ•œ ์ดˆ๊ธฐ ๋ฒ•๋ž‘์งˆ์˜ ์žฌ๊ด‘ํ™” ํšจ๊ณผ๋ฅผ ๊ด‘ํ•™์ ์œผ๋กœ ํ‰๊ฐ€ํ•˜๊ธฐ ์œ„ํ•˜์—ฌ Quantitative Laser Fluorescence (QLF)๋ฅผ ์ด์šฉํ•˜์˜€๋‹ค. ๊ฑด์ „ ์น˜์•„์™€ ๋น„๊ตํ•ด์„œ ์ดˆ๊ธฐ ๋ฒ•๋ž‘์งˆ ์šฐ์‹ ์žฌ๊ด‘ํ™”์˜ ์ฐจ์ด๋ฅผ ํƒ์ง€ํ•˜๊ธฐ ์œ„ํ•ด์„œ ์‹œํŽธ์˜ window ๋ถ€์œ„๋ฅผ ์ค‘์‹ฌ์œผ๋กœ QLF๋ฅผ ์ด์šฉํ•˜์—ฌ fluorescence loss (?F, %), lesion size (ใŽœ2), ?Q (%ร—ใŽœ2) ๊ฐ’์„ ์–ป์—ˆ์œผ๋ฉฐ Confocal Laser Scanning Microscopy (CLSM) ๊ด€์ฐฐ์„ ํ†ตํ•˜์—ฌ fluorescent lesion์˜ ๊นŠ์ด์™€ intensity ๋“ฑ ๋ณ‘์†Œ์˜ ๊นŠ์ด ๋ณ€ํ™”๋ฅผ ๊ด€์ฐฐํ•˜์˜€๋‹ค. ๋˜ํ•œ Scanning Electron Microscope (SEM)์„ ์ด์šฉํ•˜์—ฌ ์ž…์ž์˜ ํฌ๊ธฐ์— ๋”ฐ๋ฅธ ๊ฒฐ์ •๊ตฌ์กฐ๋ฅผ ์‚ดํŽด๋ณด๊ณ  ์žฌ๊ด‘ํ™” ์–‘์ƒ์„ ๋ถ„์„ํ•˜์˜€์œผ๋ฉฐ ๋‹ค์Œ๊ณผ ๊ฐ™์€ ๊ฒฐ๊ณผ๋ฅผ ์–ป์—ˆ๋‹ค. 1. pH ์ˆœํ™˜ ๋ชจํ˜•์„ ํ†ตํ•œ ๋ฒ•๋ž‘์งˆ ํ‘œ๋ฉด์˜ ๋ฏธ์„ธ๊ฒฝ๋„ ๋ณ€ํ™”๋ฅผ ์‚ดํŽด ๋ณธ ๊ฒฐ๊ณผ 5% n-CAP๊ตฐ์ด ? VHN ๊ฐ’์ด 23.16ยฑ9.99 ๋กœ ๋‹ค๋ฅธ n-CAP๊ตฐ๋ณด๋‹ค ํ‘œ๋ฉด ๊ฒฝ๋„๊ฐ€ ๋” ๋†’๊ฒŒ ๋‚˜ํƒ€๋‚ฌ๋‹ค(p<0.05). 2. ๋ฒ•๋ž‘์งˆ ํ‘œ์ธต ํ•˜๋ถ€์˜ ์นจํˆฌ์œจ์„ ์‹ฌ๋ถ€๋กœ์˜ ๋ฌด๊ธฐ์งˆ ์†Œ์‹ค์ •๋„๋กœ ์ธก์ •ํ•œ ๊ฒฐ๊ณผ์—์„œ๋Š” 10%์˜ CPP-ACP ๊ตฐ์—์„œ ?Z 1014.9ยฑ342.8(Under Vol 85% area)๋กœ KHN์˜ ํ‰๊ท ๊ฐ’์ด ๊ฐ€์žฅ ์ ๊ฒŒ ๋‚˜ํƒ€๋‚˜ 10% CPP-ACP์—์„œ ๋ณ‘์†Œ ์‹ฌ๋ถ€๋กœ ๊ฐˆ์ˆ˜๋ก ๋ฌด๊ธฐ์งˆ์˜ ์†Œ์‹ค ์ •๋„๊ฐ€ ๋‚ฎ์€ ๊ฒƒ์œผ๋กœ ๋‚˜ํƒ€๋‚ฌ๋‹ค(p<0.05). 3. QLF๋ฅผ ์ด์šฉํ•œ ์šฐ์‹๋ณ‘์†Œ์˜ ๊นŠ์ด ๋ณ€ํ™” ์ธก์ •์—์„œ๋Š” lesion(mm2)์˜ mineral loss, ์ฆ‰ ?Q๊ฐ’์ด 10%์˜ n-CAP์—์„œ ์šฐ์‹๋ณ‘์†Œ์˜ ๊นŠ์ด๊ฐ€ ๋‚ฎ์€ ๊ฒƒ(?Q -6.58ยฑ7.37)์œผ๋กœ ๋‚˜ํƒ€๋‚ฌ์œผ๋‚˜ ํ†ต๊ณ„์ ์œผ๋กœ ์œ ์˜ํ•˜์ง€ ์•Š์•˜๋‹ค(p>0.05). 4. CLSM๊ณผ SEM์„ ์ด์šฉํ•˜์—ฌ ๋ฒ•๋ž‘์งˆ ํ‘œ๋ฉด์˜ ์–‘์ƒ๊ณผ ์šฐ์‹๋ณ‘์†Œ์˜ ๋ฌด๊ธฐ์งˆ ์นจ์ฐฉ ์ •๋„๋ฅผ ์‚ดํŽด๋ณธ ๊ฒฐ๊ณผ ์šฐ์‹๋ณ‘์†Œ์˜ ๊นŠ์ด์™€ ํ‘œ๋ฉด ๊ฒฝ๋„๋ณ€ํ™” ์‚ฌ์ด์—์„œ 5% n-CAP๊ตฐ์ด 45.27ยฑ9.99 ใŽ›, 10% n-CAP๊ฐ€ 43.35ยฑ6.55 ใŽ›๋กœ 10% n-CAP๊ตฐ์ด ๋‹ค๋ฅธ ๊ตฐ๋“ค์— ๋น„ํ•ด ๋ณ‘์†Œ ๊นŠ์ด์˜ ๊ฐ์†Œ๋ฅผ ๋‚˜ํƒ€๋ƒˆ์ง€๋งŒ ์œ ์˜ํ•œ ์ฐจ์ด ์—†์—ˆ๋‹ค (p>0.05). ๋˜ํ•œ SEM์„ ์ด์šฉํ•˜์—ฌ ๋ฒ•๋ž‘์งˆ ํ‘œ๋ฉด์˜ ์–‘์ƒ์„ ์‚ดํŽด๋ณธ ๊ฒฐ๊ณผ ๊ฐ ๊ตฐ ๊ฐ„์— ํŠน์ดํ•œ ์†Œ๊ฒฌ์€ ์—†์—ˆ์œผ๋‚˜ ์ „๋ฐ˜์ ์œผ๋กœ ํ‘œ๋ฉด์— ์นจ์ฐฉ๋œ ์–‘์ƒ์„ ๋„์—ˆ๋‹ค. ์ด์ƒ์˜ ์‹คํ—˜๊ฒฐ๊ณผ๋ฅผ ์ข…ํ•ฉํ•ด ๋ณผ ๋•Œ nano-sized Carbonate Apatite๋Š” ๋ฒ•๋ž‘์งˆ ํ‘œ๋ฉด์ธต์—์„œ ์žฌ๊ด‘ํ™” ํšจ๊ณผ๊ฐ€ ์žˆ์—ˆ์œผ๋ฉฐ CPP-ACP๋Š” ๋ฒ•๋ž‘์งˆ ํ‘œ๋ฉด ํ•˜์ธต์—์„œ ์žฌ๊ด‘ํ™” ํšจ๊ณผ๊ฐ€ ์žˆ์Œ์„ ์•Œ ์ˆ˜ ์žˆ์—ˆ๋‹ค. ํ‘œ์ธต๊ณผ ์‹ฌ๋ถ€์—์„œ์˜ ์žฌ๊ด‘ํ™” ์–‘์ƒ์ด ๋‹ฌ๋ผ์ง„ ๊ฒƒ์€ CPP-ACP์˜ ๊ฒฝ์šฐ ํƒˆํšŒ๋œ ํ‘œ๋ฉด์—์„œ์˜ ๋ฌด๊ธฐ์งˆ ๊ฐ์†Œ ๋ถ€์œ„์— ์นผ์Š˜๊ณผ ์ธ ๋“ฑ์˜ ์ด์˜จ์ด ์šฉํ•ด๋˜์—ˆ๋‹ค๊ฐ€ ์„์ถœ๋˜๋Š” ๊ณผ์ •์—์„œ ์ธ ๋‹จ๋ฐฑ์งˆ์ธ Casein phosphopeptide ์œ ๊ธฐ๋ฌผ์ด ์šด๋ฐ˜์ฒด ์—ญํ• ์„ ํ•˜์—ฌ ์นผ์Š˜๊ณผ ์ธ ๋“ฑ์˜ ์ด์˜จ์„ ๋ณ‘์†Œ ์‹ฌ๋ถ€๊นŒ์ง€ ์ „๋‹ฌํ•œ ๊ฒƒ์œผ๋กœ ์ถ”์ •๋˜๋ฉฐ n-CAP์˜ ๊ฒฝ์šฐ๋Š” ๋ฌด๊ธฐ์งˆ ์นจ์ฐฉ์ด ํ‘œ์ธต ๋ถ€์œ„์— ๊ตญํ•œ๋˜์–ด ํ‘œ๋ฉด์ธต์— ์นจ์ฐฉ๋œ ์นผ์Š˜๊ณผ ์ธ ๋“ฑ์˜ ์ด์˜จ์ด ์‹ฌ๋ถ€๋กœ์˜ ์นจํˆฌ๋ฅผ ๋ฐฉํ•ดํ•˜์—ฌ ์‹ฌ๋ถ€๊นŒ์ง€์˜ ์™„์ „ํ•œ ์žฌ๊ด‘ํ™”๊ฐ€ ์ผ์–ด๋‚˜์ง€ ์•Š์•˜์Œ์„ ์œ ์ถ”ํ•  ์ˆ˜ ์žˆ๋‹ค. ์ด์— n-CAP์˜ ์žฌ๊ด‘ํ™” ํšจ๊ณผ๋ฅผ ์ฆ์ง„์‹œํ‚ค๊ธฐ ์œ„ํ•œ ํ–ฅํ›„ ์—ฐ๊ตฌ์—์„œ๋Š” CPP-ACP์˜ casein๊ณผ ๊ฐ™์€ ํ™œ์„ฑ์ฒด ์—ญํ• ์„ ํ•  ์ˆ˜ ์žˆ๋Š” ์œ ๊ธฐ๋ฌผ์งˆ์— ๋Œ€ํ•œ ๊ณ ๋ ค๊ฐ€ ์žˆ์–ด์•ผ ํ•˜๋ฆฌ๋ผ ์—ฌ๊ฒจ์ง„๋‹ค. [์˜๋ฌธ] Dental caries are the most common disease leading to tooth damage; they cause this through lysis of minerals and organic substances. When the balance of mineral exchange is maintained, dental caries can be prevented by blocking demineralization. Hence, healthy teeth can be successfully maintained. The aim of this study was to evaluate the remineralization effects of nano-sized carbonate apatite (n-CAP) and to compare it with casein phosphopeptide amorphous-calcium phosphate (CPP-ACP). The concentrations of n-CAP were classified into 0%, 5%, 10%. We use Tooth MousseTM, which is marketed with 10% CPP-ACP. Specimens were prepared from extracted bovine incisal teeth that were free of caries and defects. In this study, we sought to compare the remineralization effects of n-CAP and CPP-ACP on early caries lesions in enamel using a pH-cycling model for 14 days. The enamel specimens were immersed in each solution. Enamel specimens that had Vickers Hardness Numbers (VHN) of 40~80 were selected for artificial demineralization for 48 hours. All specimens were evaluated by measuring the VHN of the enamel surface at each step using the microhardness test (JT, Toshi Inc, Japan). The hardness of the enamel was measured before and after the processing remineralization, and the degree of mineral loss (vol %) was measured as ฮ”Z using the Knoop Hardness Number (KHN) to determine the effect of lesion depth on remineralization. Likewise, Quantitative Laser Fluorescence (QLF) was used to perform optic quantitative evaluation of early enamel. QLF was focused on a window area to detect the remineralization differences of early enamel caries through comparison with healthy teeth. Fluorescence loss (ฮ”F,%), lesionsize (ใŽœ2), and ฮ”Q (%ร—ใŽœ2) value were determined through this process, and the depth of lesions such as fluorescent lesions was observed using Confocal Laser Scanning Microscopy (CLSM). Lesion intensity was determined, as well. Moreover, we used a Scanning Electron Microscope (SEM) to examine the crystal structure according to the size of the particles and to analyze the features of remineralization. The following are the results of this study: 1. On observing changes in the surface microhardness of the enamel using pH cycling, we noted that the 5% n-CAP group had much higher ฮ”VHN(23.16ยฑ9.99) than did the other n-CAP groups (p<0.05). 2. On measuring the mineral loss of deep enamel lesions, we noted that the 10% CPP-ACP groups exhibited lower mineral loss per the KHN (ฮ”Z=1014.9ยฑ342.8, under vol 85% area) than did the other groups (p<0.05). 3. When measuring the depth changes of caries using QLF, 10% n-CAP showed a greater decrease in lesion depth than did the other groups. However, there was no statistically significant difference among these 4 groups (p>0.05). 4. The features of the enamel surfaces and the degree of mineral deposition in the cavity were observed using CLSM and SEM. Concerning the cavity depth and surface hardness changes, the depth in the 10% n-CAP group was lower than that seen in the other groups, but was not significantly different (p>0.05). Moreover, SEM showed no specific features on examination of the enamel surfaces, but there was a general deposition on the surfaces. Based on that data from this study, it can be concluded that: (1) nano-sized carbonate apatite had the effect of remineralization on the enamel surface layer, and CPP-ACP had the effect of remineralization underneath the enamel surface; (2) differences in remineralization aspects on the surface and in the deep layers are presumed to be secondary to casein phosphopeptide organic material precipitation on areas with mineral reduction during dissolution of ions such as calcium and phosphate. Hence, in future studies dedicated to improving the remineralization effect of n-CAP, organic materials such as casein should be considered proactivators.ope

    Effect of ketamine on the isolated uterus of guinea pig

    No full text
    ์˜ํ•™๊ณผ/์„์‚ฌ[ํ•œ๊ธ€] ์‚ฐํ›„ ์ž๊ถ์ถœํ˜ˆ์€ ๋ชจ์ฒด์‚ฌ๋ง์˜ ์ค‘์š”ํ•œ ์›์ธ์ด ๋˜๋ฉฐ ๋Œ€๋ถ€๋ถ„์˜ ๊ฐ•๋ ฅํ•œ ํก์ž…๋งˆ์ทจ์ œ๋Š” ์ž๊ถ์ˆ˜ ์ถ•์˜ ์žฅ์• ๋ฅผ ์ผ์œผํ‚ค๋ฏ€๋กœ ๋ฌธ์ œ์‹œ ๋˜๊ณ ์žˆ๋‹ค(Munson, 1970: ไปป๋“ฑ, 1971: ้‡‘, 1972). ์ž„์ƒ์ ์œผ๋กœ ketamine์€ ์ž๊ถ์ˆ˜์ถ•์„ ์ด‰์ง„์‹œํ‚จ๋‹ค(Chodoff ๋ฐ Stella, 1966: Little๋“ฑ, 1 972; Galbert ๋ฐ Gardner, 1973; Corssen 1974)๊ณ  ๋ณด๊ณ ๋œ๋ฐ” ์žˆ์œผ๋ฉฐ, Jawalekar ๋“ฑ(1972) ์€ ์ฅ์˜ ์ž„์‹ ์ž๊ถ์ ˆํŽธ์— ketamine์„ ์ ์šฉํ•˜์—ฌ ์ž๊ถ์šด๋™์˜ ์ด‰์ง„์„ ๊ด€์ฐฐํ•˜์˜€๋‹ค. ้‡‘(1975)์— ์˜ํ•˜๋ฉด ๊ฐ€ํ† ์—์„œ ketamine์˜ ์ž๊ถ์šด๋™ ์ด‰์ง„์ž‘์šฉ์€ adrenergic ๋ฐ cholinergic receptor ์™€ ๊ด€๊ณ„์—†์ด ๋‚œ์†Œํ˜ธ๋ฅด๋ชฌ์ค‘ ์ฃผ๋กœ progesterone์˜ ์˜ํ–ฅ์„ ๋ฐ›์œผ๋ฉฐ ์ž๊ถ๊ทผ์— ๋Œ€ํ•˜์—ฌ ์ง์ ‘์ ์œผ ๋กœ ์ž‘์šฉํ•œ๋‹ค๊ณ  ํ–ˆ๋‹ค. ์ด์— ์ €์ž๋Š” ketamine์ด ํ•ด๋ช…(guinea pig)์˜ ์ž๊ถ์— ๋Œ€ํ•ด์„œ๋„ ์ด‰์ง„์ž‘์šฉ์„ ๋‚˜ํƒ€๋‚ด๋Š”์ง€์˜ ์—ฌ๋ถ€์— ๊ด€ํ•ด ์ถ”๊ตฌํ•จ๊ณผ ๋™์‹œ์— ketamine์ด ํ•ด๋ช…์—์„œ๋„ progesterone์˜ ์˜ํ–ฅ์„ ๋ฐ›๋Š”์ง€๋ฅผ ์ถ”์‹œํ–ˆ๋‹ค. ์‹คํ—˜๋™๋ฌผ๋กœ๋Š” 0.5ใŽ๋‚ด์™ธ์˜ ๋น„์ž„์„ฑ์ˆ™์ž์„ฑํ•ด๋ช…(้žๅฆŠๆˆ็†Ÿ้›Œๆ€งๆตทๆบŸ)๊ณผ 2.0ใŽ๋‚ด์™ธ์˜ ๋น„์ž„์„ฑ ์ˆ™์ž์„ฑ๊ฐ€ํ† (้žๅง™ๆˆ็†Ÿ้›Œๆ€งๅฎถใ€€)์„ ์‚ฌ์šฉํ•˜์˜€๋‹ค. ํ•ด๋ช…๊ณผ ๊ฐ€ํ† ๋Š” ๊ฐ๊ฐ ์–‘์ธก๋‚œ์†Œ์ ์ถœ 10โˆผ14์ผ ํ›„ estrogen์ฃผ์‚ฌ๊ตฐ์€ estradiol benzoate 2,000 I.U./ใŽ, progesterone์ฃผ์‚ฌ๊ตฐ์€ progeste rone 5ใŽŽ/ใŽ์„ ๋งค์ผ 1ํšŒ 4์ผ๊ฐ„ ๊ทผ์œก์ฃผ์‚ฌํ–ˆ๋‹ค. ์ž๊ถ์ ˆํŽธ(1.5โˆผ2.0ใŽ ๊ธธ์ด)์€ ํ•ด๋ช… ํ˜น์€ ๊ฐ€ํ† ์—์„œ ๋„์‚ดํ•˜๋Š” ์ฆ‰์‹œ ๋ถ„๋ฆฌ ์ฒ™์ถœ(ๅ‰”ๅ‡บ)ํ•˜์—ฌ Locke์•ก 50ใŽ–๊ฐ€ ๋“ค์–ด์žˆ๋Š” ์ด์ค‘๋ฒฝ์ดˆ์ž์ œ(ไบŒ้‡ๅฃ็กๅญ่ฃฝ) muscle chamber ์ €๋ถ€(ๅบ•้ƒจ)์— ํ•œ๊ณจ ์„ ๊ณ ์ •ํ•˜๊ณ  ๋‹ค๋ฅธ๋์€ lever์— ์—ฐ๊ฒฐํ•˜์—ฌ ๊ทธ ์ˆ˜์ถ•์„ kymograph์ง€์— ๋ฌ˜์‚ฌํ•˜์˜€๋‹ค. ์ด๋•Œ musc le chamber๋‚ด Locke์•ก์€ 38โ„ƒ๋กœ ์ผ์ •ํ•˜๊ฒŒ ์œ ์ง€์‹œํ‚ค๊ณ  ์‚ฐ์†Œ๋ฅผ ๊ณ„์† ๊ณต๊ธ‰ํ–ˆ๋‹ค. ์ž๊ถ์ ˆํŽธ์˜ ์ž๋ฐœ์šด๋™์ด ์ผ์ •ํ•˜๊ฒŒ ๋จ์„ ๊ธฐ๋‹ค๋ ค ketamine์„ ์ ์šฉํ•˜๊ณ  ์šด๋™๊ณก์„ ์˜ ๋ณ€ํ™”๋ฅผ ๊ด€์ฐฐํ•˜์˜€๋˜๋ฐ” ๋‹ค์Œ๊ณผ ๊ฐ™์€ ๊ฒฐ๊ณผ๋ฅผ ์–ป์—ˆ๋‹ค. 1) ํ•ด๋ช…์˜ ์ž๊ถ์šด๋™์–‘์ƒ์€ ๊ฐ€ํ† ์™€๋Š” ๋‹ฌ๋ฆฌ ๋†’์€ ์ˆ˜์ถ•๊ณ ์™€ ์ ์€ ์ˆ˜์ถ•๋นˆ๋„๋ฅผ ๋‚˜ํƒ€๋‚ด์—ˆ๋‹ค. 2) Estrogen์ฃผ์‚ฌ ํ•ด๋ช…์ž๊ถ์ ˆํŽธ์— 1โˆผ25 ฮณ/ใŽ–์˜ ketamine์„ ์ ์šฉํ•˜์˜€๋˜๋ฐ” ์ž๊ถ์šด๋™์–‘์ƒ ์— ์•„๋ฌด๋Ÿฐ ๋ณ€ํ™”๊ฐ€ ์—†์—ˆ๊ณ  50 ฮณ/ใŽ–์ด์ƒ์˜ ๋Œ€๋Ÿ‰์„ ์ ์šฉํ•˜์˜€์„ ๋•Œ๋Š” ์˜คํžˆ๋ ค ์ž๊ถ์ˆ˜์ถ•๊ณ ์˜ ์ €ํ•˜๋ฅผ ๋‚˜ํƒ€๋‚ด์—ˆ๋‹ค. 3) Progesterone์ฃผ์‚ฌ ํ•ด๋ช…์ž๊ถ์ ˆํŽธ์— 1โˆผ100 ฮณ/ใŽ–์˜ ketamine์„ ์ ์šฉํ•˜์˜€๋˜ ์•„๋ฌด๋Ÿฐ ๋ฐ˜ ์‘์ด ์—†์—ˆ์œผ๋‚˜ estrogenํˆฌ์—ฌ๊ตฐ์˜ 3๋ฐฐ์˜ ์–‘์ธ 150 ฮณ/ใŽ–์˜ ๋†๋„์—์„œ ์—ญ์‹œ ์ž๊ถ์ˆ˜์ถ•๊ณ ์˜ ์ € ํ•˜๋ฅผ ๋‚˜ํƒ€๋ƒˆ์œผ๋ฉฐ 200 ฮณ/ใŽ–์˜ ๋†๋„์—์„œ๋Š” ํ˜„์ €ํ•œ ์–ต์ œ๋ฅผ ๋ณด์—ฌ์ฃผ์—ˆ๋‹ค. 4) Estrogen์ฃผ์‚ฌ ๊ฐ€ํ† ์ž๊ถ์ ˆํŽธ์— ๋Œ€ํ•œ ๋Œ€๋Ÿ‰์˜ ketamine์˜ ์˜ํ–ฅ์€ 20 ฮณ/ใŽ–์˜ ๋†๋„์—์„œ ๋Š” ์•„๋ฌด ๋ณ€ํ™”๊ฐ€ ์—†์—ˆ์œผ๋‚˜ ํ•ด๋ช…์ž๊ถ์ ˆํŽธ์—์„œ ์ˆ˜์ถ•๊ณ ์˜ ์ €ํ•˜๋ฅผ ๋ณด์—ฌ์ฃผ๋Š” 50 ฮณ/ใŽ–์˜ ๋†๋„์— ์„œ๋Š” ์—ญ์‹œ ์ˆ˜์ถ•๊ณ ์˜ ์ €ํ•˜๋ฅผ ๋‚˜ํƒ€๋‚ด์—ˆ๋‹ค. 5) Progesterone์ฃผ์‚ฌ ๊ฐ€ํ† ์ž๊ถ์ ˆํŽธ์— ๋Œ€ํ•œ ๋Œ€๋Ÿ‰์˜ ketamine์˜ ์˜ํ–ฅ์„ ๋ณด์•˜๋˜๋ฐ” 150 ฮณ/ ใŽ–์˜ ๋†๋„์—์„œ๋Š” ์ˆ˜์ถ•๊ณ ์˜ ํ•ญ์ง„์„ ๋‚˜ํƒ€๋ƒˆ์œผ๋‚˜ 200 ฮณ/ใŽ–์˜ ๋†๋„์—์„œ๋Š” ์—ญ์‹œ ์ˆ˜์ถ•๊ณ ์˜ ์ € ํ•˜๋ฅผ ๋‚˜ํƒ€๋ƒˆ๋‹ค. ์ด์ƒ์˜ ๊ฒฐ๊ณผ, ketamine์˜ ์ž๊ถ์ˆ˜์ถ•์ž‘์šฉ์€ ๊ฐ€ํ† ์— ์žˆ์–ด์„œ๋Š” progesterone์˜ ์˜ํ–ฅ์„ ๋ฐ›์œผ ๋‚˜ ํ•ด๋ช…์— ์žˆ์–ด์„œ๋Š” progesterone์˜ ์˜ํ–ฅ์„ ๋šœ๋ ท์ด ๊ด€์ฐฐํ•  ์ˆ˜๋Š” ์—†์—ˆ๋‹ค. ์ฆ‰ ์ข…์กฑ์ฐจ์ด๊ฐ€ ์žˆ๋‹ค๊ณ  ์ƒ๊ฐํ•  ์ˆ˜ ์žˆ์—ˆ๋‹ค. ๊ทธ๋ฆฌ๊ณ  ketamine์„ ๋Œ€๋Ÿ‰ ์ ์šฉํ•˜๊ฒŒ ๋˜๋ฉด ์ž๊ถ์ˆ˜์ถ•๊ณ ์˜ ์–ต์ œํ˜„์ƒ ์ด ๋‚˜ํƒ€๋‚˜๋Š”๋ฐ ๊ทธ ์–ต์ œ๋Ÿ‰์€ ํ•ด๋ช… ๋ฐ ๊ฐ€ํ†  ๋ชจ๋‘ estrogenํˆฌ์—ฌ๊ตฐ๋ณด๋‹ค progesteroneํˆฌ์—ฌ๊ตฐ์— ์žˆ์–ด์„œ ๋” ๋Œ€๋Ÿ‰์ด ํ•„์š”ํ•จ์„ ๋ณผ ์ˆ˜ ์žˆ์—ˆ๋‹ค. [์˜๋ฌธ] Postpartum bleeding of the uterus is an important cause of maternal death. It is thought that the inhibitory effect of the majority of potent inhalation anesthetics on uterine contractions is often responsible (Munson, 1970; Lim et al., 1971; Kim, 1972). There have been numerous reports that ketamine stimulates uterine contraction clinically (Chodoff and Stella, 1966; Little et al, 1972; Galbert and Gardner, 1973; Corssen, 1974). Jawalekar and associates (1972) reported that ketamine increased resting tension, contractile amplitude and frequency of the uterine strips of pregnant mice, and Kim (1975) reported research on the effects of ketamine on the isolated uterus of rabbits. According to Kim (1975), ketamine exerted a stimulatory action on the uterus under the influence of progesterone. This progesterone-dependent uterine stimulatory action of ketamine is not concerned with adrenergic and cholinergic mechanisms but appears to have a direct effect on the uterine muscle. The present study was undertaken to determine whether or not ketamine also exerted a stimulatory action on the uterus of the guinea pig and to follow up whether or not stimulatory action of ketamine also depends upon progesterone in the guinea pig. Adult female non-pregnant guinea pigs and rabbits weighing approximately 0.5 kg and 2.0 kg respectively were employed in this experiment. At the end of 10 to 14 days following bilateral oophorectomy, non-pregnant guinea pigs and rabbits were injected intramusculary with estradiol benzoate (2,000 I.U./kg) or progesterone (5 mg/kg) once a day for four consecutive days. A uterine strip, about 1.5-2.0 cm in length, was carefully isolated from the experimental animals and suspended in a muscle chamber containing 50 ml of Locke's solution, maintained at constant temperature of 38โ„ƒ. It was aerated with 100% oxygen bubbling through the bathing fluid by means of a sintered glass plate at the bottom of the muscle chamber. One end of the uterine strip was attached to the bottom of the muscle chamber and the other end to a lever. Motility and tonus were recorded on kymograph paper. After being washed several times with fresh Locke's solution, the uterine strip attained a constant motility and tonus. Ketamine then was added ion various concentrations to the chamber. The results are as follows: 1. The uterine motility of guinea pig shows a higher amplitude and lower frequency compared with that of rabbit. 2. Effects of ketamine on isolated uterine strips of guinea pig pre-treated with estrogen showed no change using 1-20 ฮณ/ml of ketamine, but with 50 ??/ml or more, the amplitude of uterine contractions was depressed. 3. On isolated uterine strips of guinea pig pre-treated with progesterone, there was no effect with 1-100 ฮณ/ml of ketamine, depressed amplitude of uterine contractions with 150 ฮณ/ml and markedly depressed amplitude of uterine contraction with 200 ฮณ/ml. 4. On isolated uterine strips of rabbit pre-treated with estrogen, there was no effect with 20 ฮณ/ml of ketamine, but depressed amplitude of uterine contraction using 50 ฮณ/ml. 5. On isolated uterine strips of rabbits pre-treated with progesterone, there was an increase in amplitude and frequency of uterine contractions with up to 150 ฮณ/ml of ketamine, but depressed amplitude with 200 ฮณ/ml or more. From the above results it may be concluded that ketamine exerted a stimulatory action on the uterus of rabbit under the influence of progesterone but not on the uterus of guinea pig. The large amount of ketamine depressed the amplitude of uterine contraction in guinea pig and rabbit, and this depressing dose is higher in the animals (guinea pig and rabbit) pre-treated with progesterone than with estrogen.restrictio
    • โ€ฆ
    corecore