240 research outputs found
Association between thyroid hormones and the components of metabolic syndrome
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
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
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
์ฑ์ฅํธ๋ฅด๋ชฌ ๋ถ๋น ๋ํ์์ฒด ์ข ์์ ์์ ์ ์์น ํ ๋ฐ๊ฒฌ๋ ์ง์ฐํ ์๊ฐ๋ฉด์ญ ๋น๋จ๋ณ 1์
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
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
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
้ซ็ณป็ ๅฑ้ช์ ํ์ค์ ์ ๊ทผ๋ฒ๊ณผ ์ด๋ฅผ ์ด์ฉํ ์ฑ๊ณผ์ธก์
1980-03ไผๆฅญ่ฒกๅ์ ็ฎๆจ๋ ไผๆฅญ์ ๅนๅค๋ฅผ ๆๅคงๅํจ์ผ๋ก์จ ๆ ชไธป์ ๅฏ๋ฅผ ๆฅตๅคงๅ์ํค๋ ๊ฒ์ด๋ค. ๊ทธ๋ฌ๋ ไผๆฅญ์ด ๅนๅค่ฟฝๆฑ๋ฅผ ์ํ์ฌ ๆ่ณๆฑบๅฎ์ ํ ๋๋ ํญ์ ๆๅพ
๋๋ ๆ่ณๆถ็๊ณผ ๋๋ถ์ด ๅฑ้ช์ด ๋ฐ๋ฅด๊ธฐ ๋ง๋ จ์ด๋ค.
ๅฑ้ช์ด ์ด๋ค ๆๅณ๋ฅผ ๊ฐ์ง๊ณ ์๋๋ ํ๋ ๊ฒ์ ๊ดํ์ฌ๋ ๋ค์ ่ฆ่งฃ์ ์ฐจ์ด๋ ์์ผ๋, ์ ์ด๋ ๅฑ้ช์ ๆชไพ่ฑซๆธฌ์ ๋ํ ไธๅฎๅ
จๆง์์ ์ค๋ ๊ฒ์ผ๋ก ไธ็ขบๅฏฆๆง์ ๊ธฐ์ธํ๋ค๊ณ ๋ณผ ์ ์๋ค. ๆ่ณๅฎถ์ ๅฑ้ช์ ๆชไพ์ ็พ้ํ๋ฆ์ด๋ ๊ฐ๋ฅํ ๆถ็์ ๅๆฃ็จๅบฆ(variability of possible return)๋ฅผ ๋งํ๋ฉฐ, ๆชไพ์ ๋ํ ไธ็ขบๅฏฆ๋ก ์ธํ์ฌ ๅฏ่ฝํ ๆถ็์ด ๅนณๅๅค์ ์ ์ดํํ๋ ์ ๋๋ฅผ ๋งํ๋ค
(The) effect of nano-sized carbonate apatite on remineralization of artificial caries-like lesions
์น์ํ๊ณผ/๋ฐ์ฌ[ํ๊ธ]
์น์์ฐ์์ฆ์ ๋ฌด๊ธฐ์ง ์ฉํด์ ์ ๊ธฐ์ง ํ๊ดด๋ก ์น์์์์ด ์ผ์ด๋๋ ๊ตฌ๊ฐ์์ญ์์ ๋ํ๋๋ ๊ฐ์ฅ ๋ํ์ ์ธ ์งํ์ผ๋ก ๋ฌด๊ธฐ์ง ๊ตํ์ ํํ์ ์ ์ง์์ผ ์ค๋ค๋ฉด ํํ๋ฅผ ๋ฐฉ์งํ์ฌ ์น์์ฐ์์ฆ์ ์๋ฐฉํ ์ ์์ผ๋ฉฐ ์น์๋ฅผ ๊ฑด๊ฐํ๊ฒ ์ ์งํ ์ ์๋ค.
๋ณธ ์ฐ๊ตฌ๋ ์ด๊ธฐ ๋ฒ๋์ง ์ฐ์์ ํ๋ณต๊ณผ ์น์์ ์ฌ๊ดํ๋ฅผ ์ ๋ํ๊ธฐ ์ํ์ฌ ์ธ๊ณต ์ด๊ธฐ ์ฐ์๋ณ์๋ฅผ ํ์ฑํ ๋ฒ๋์ง์ nano-sized Carbonate Apatite(n-CAP)์ ์ฌ๊ดํ ํจ๊ณผ๋ฅผ Casein Phosphopeptide Amorphous-Calcium Phosphate(CPP-ACP)์ ์ํธ ๋น๊ตํ์ฌ ๋ถ์ํ์๋ค.
n-CAP์ ๋๋๋ 0%, 5%, 10%๋ก ๊ตฌ๋ถํ์์ผ๋ฉฐ CPP-ACP๋ 10% ํจ์ ๋์ด ์ํ๋๊ณ ์๋ Tooth MousseTM ๋ฅผ pH ์ํ๋ชจ๋ธ์ ์ด์ฉํ์ฌ 14์ผ๊ฐ ๊ฐ๊ฐ ํ๋ฃจ 3ํ์ฉ 5๋ถ๊ฐ ์ฒ๋ฆฌํ์์ผ๋ฉฐ ์ฒ๋ฆฌ ์ , ํ์ ํ๋ฉด์ ๊ฒฝ๋ ๋ณํ๋ฅผ Vickers Hardness Number (VHN)๋ก ํ๊ฐํ์๊ณ Knoop Hardness number (KHN)๋ก ๋ฌด๊ธฐ์ง์ ์์ค์ ๋(vol %)๋ฅผ ?Z ๊ฐ์ผ๋ก ์ธก์ ํ์ฌ ๋ณ์ ์ฌ๋ถ๋ก์ ์ฌ๊ดํ์ ๋ฏธ์น ์ํฅ์ ์ดํด๋ณด์๋ค. ๋ํ ์ด๊ธฐ ๋ฒ๋์ง์ ์ฌ๊ดํ ํจ๊ณผ๋ฅผ ๊ดํ์ ์ผ๋ก ํ๊ฐํ๊ธฐ ์ํ์ฌ Quantitative Laser Fluorescence (QLF)๋ฅผ ์ด์ฉํ์๋ค. ๊ฑด์ ์น์์ ๋น๊ตํด์ ์ด๊ธฐ ๋ฒ๋์ง ์ฐ์ ์ฌ๊ดํ์ ์ฐจ์ด๋ฅผ ํ์งํ๊ธฐ ์ํด์ ์ํธ์ window ๋ถ์๋ฅผ ์ค์ฌ์ผ๋ก QLF๋ฅผ ์ด์ฉํ์ฌ fluorescence loss (?F, %), lesion size (ใ2), ?Q (%รใ2) ๊ฐ์ ์ป์์ผ๋ฉฐ Confocal Laser Scanning Microscopy (CLSM) ๊ด์ฐฐ์ ํตํ์ฌ fluorescent lesion์ ๊น์ด์ intensity ๋ฑ ๋ณ์์ ๊น์ด ๋ณํ๋ฅผ ๊ด์ฐฐํ์๋ค. ๋ํ Scanning Electron Microscope (SEM)์ ์ด์ฉํ์ฌ ์
์์ ํฌ๊ธฐ์ ๋ฐ๋ฅธ ๊ฒฐ์ ๊ตฌ์กฐ๋ฅผ ์ดํด๋ณด๊ณ ์ฌ๊ดํ ์์์ ๋ถ์ํ์์ผ๋ฉฐ ๋ค์๊ณผ ๊ฐ์ ๊ฒฐ๊ณผ๋ฅผ ์ป์๋ค.
1. pH ์ํ ๋ชจํ์ ํตํ ๋ฒ๋์ง ํ๋ฉด์ ๋ฏธ์ธ๊ฒฝ๋ ๋ณํ๋ฅผ ์ดํด ๋ณธ ๊ฒฐ๊ณผ 5% n-CAP๊ตฐ์ด ? VHN ๊ฐ์ด 23.16ยฑ9.99 ๋ก ๋ค๋ฅธ n-CAP๊ตฐ๋ณด๋ค ํ๋ฉด ๊ฒฝ๋๊ฐ ๋ ๋๊ฒ ๋ํ๋ฌ๋ค(p<0.05).
2. ๋ฒ๋์ง ํ์ธต ํ๋ถ์ ์นจํฌ์จ์ ์ฌ๋ถ๋ก์ ๋ฌด๊ธฐ์ง ์์ค์ ๋๋ก ์ธก์ ํ ๊ฒฐ๊ณผ์์๋ 10%์ CPP-ACP ๊ตฐ์์ ?Z 1014.9ยฑ342.8(Under Vol 85% area)๋ก KHN์ ํ๊ท ๊ฐ์ด ๊ฐ์ฅ ์ ๊ฒ ๋ํ๋ 10% CPP-ACP์์ ๋ณ์ ์ฌ๋ถ๋ก ๊ฐ์๋ก ๋ฌด๊ธฐ์ง์ ์์ค ์ ๋๊ฐ ๋ฎ์ ๊ฒ์ผ๋ก ๋ํ๋ฌ๋ค(p<0.05).
3. QLF๋ฅผ ์ด์ฉํ ์ฐ์๋ณ์์ ๊น์ด ๋ณํ ์ธก์ ์์๋ lesion(mm2)์ mineral loss, ์ฆ ?Q๊ฐ์ด 10%์ n-CAP์์ ์ฐ์๋ณ์์ ๊น์ด๊ฐ ๋ฎ์ ๊ฒ(?Q -6.58ยฑ7.37)์ผ๋ก ๋ํ๋ฌ์ผ๋ ํต๊ณ์ ์ผ๋ก ์ ์ํ์ง ์์๋ค(p>0.05).
4. CLSM๊ณผ SEM์ ์ด์ฉํ์ฌ ๋ฒ๋์ง ํ๋ฉด์ ์์๊ณผ ์ฐ์๋ณ์์ ๋ฌด๊ธฐ์ง ์นจ์ฐฉ ์ ๋๋ฅผ ์ดํด๋ณธ ๊ฒฐ๊ณผ ์ฐ์๋ณ์์ ๊น์ด์ ํ๋ฉด ๊ฒฝ๋๋ณํ ์ฌ์ด์์ 5% n-CAP๊ตฐ์ด 45.27ยฑ9.99 ใ, 10% n-CAP๊ฐ 43.35ยฑ6.55 ใ๋ก 10% n-CAP๊ตฐ์ด ๋ค๋ฅธ ๊ตฐ๋ค์ ๋นํด ๋ณ์ ๊น์ด์ ๊ฐ์๋ฅผ ๋ํ๋์ง๋ง ์ ์ํ ์ฐจ์ด ์์๋ค (p>0.05). ๋ํ SEM์ ์ด์ฉํ์ฌ ๋ฒ๋์ง ํ๋ฉด์ ์์์ ์ดํด๋ณธ ๊ฒฐ๊ณผ ๊ฐ ๊ตฐ ๊ฐ์ ํน์ดํ ์๊ฒฌ์ ์์์ผ๋ ์ ๋ฐ์ ์ผ๋ก ํ๋ฉด์ ์นจ์ฐฉ๋ ์์์ ๋์๋ค.
์ด์์ ์คํ๊ฒฐ๊ณผ๋ฅผ ์ข
ํฉํด ๋ณผ ๋ nano-sized Carbonate Apatite๋ ๋ฒ๋์ง ํ๋ฉด์ธต์์ ์ฌ๊ดํ ํจ๊ณผ๊ฐ ์์์ผ๋ฉฐ CPP-ACP๋ ๋ฒ๋์ง ํ๋ฉด ํ์ธต์์ ์ฌ๊ดํ ํจ๊ณผ๊ฐ ์์์ ์ ์ ์์๋ค. ํ์ธต๊ณผ ์ฌ๋ถ์์์ ์ฌ๊ดํ ์์์ด ๋ฌ๋ผ์ง ๊ฒ์ CPP-ACP์ ๊ฒฝ์ฐ ํํ๋ ํ๋ฉด์์์ ๋ฌด๊ธฐ์ง ๊ฐ์ ๋ถ์์ ์นผ์๊ณผ ์ธ ๋ฑ์ ์ด์จ์ด ์ฉํด๋์๋ค๊ฐ ์์ถ๋๋ ๊ณผ์ ์์ ์ธ ๋จ๋ฐฑ์ง์ธ Casein phosphopeptide ์ ๊ธฐ๋ฌผ์ด ์ด๋ฐ์ฒด ์ญํ ์ ํ์ฌ ์นผ์๊ณผ ์ธ ๋ฑ์ ์ด์จ์ ๋ณ์ ์ฌ๋ถ๊น์ง ์ ๋ฌํ ๊ฒ์ผ๋ก ์ถ์ ๋๋ฉฐ n-CAP์ ๊ฒฝ์ฐ๋ ๋ฌด๊ธฐ์ง ์นจ์ฐฉ์ด ํ์ธต ๋ถ์์ ๊ตญํ๋์ด ํ๋ฉด์ธต์ ์นจ์ฐฉ๋ ์นผ์๊ณผ ์ธ ๋ฑ์ ์ด์จ์ด ์ฌ๋ถ๋ก์ ์นจํฌ๋ฅผ ๋ฐฉํดํ์ฌ ์ฌ๋ถ๊น์ง์ ์์ ํ ์ฌ๊ดํ๊ฐ ์ผ์ด๋์ง ์์์์ ์ ์ถํ ์ ์๋ค.
์ด์ n-CAP์ ์ฌ๊ดํ ํจ๊ณผ๋ฅผ ์ฆ์ง์ํค๊ธฐ ์ํ ํฅํ ์ฐ๊ตฌ์์๋ CPP-ACP์ casein๊ณผ ๊ฐ์ ํ์ฑ์ฒด ์ญํ ์ ํ ์ ์๋ ์ ๊ธฐ๋ฌผ์ง์ ๋ํ ๊ณ ๋ ค๊ฐ ์์ด์ผ ํ๋ฆฌ๋ผ ์ฌ๊ฒจ์ง๋ค.
[์๋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 ฮZ 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 (ฮF,%), lesionsize (ใ2), and ฮQ (%รใ2) 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 ฮVHN(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 (ฮZ=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
์ํ๊ณผ/์์ฌ[ํ๊ธ]
์ฐํ ์๊ถ์ถํ์ ๋ชจ์ฒด์ฌ๋ง์ ์ค์ํ ์์ธ์ด ๋๋ฉฐ ๋๋ถ๋ถ์ ๊ฐ๋ ฅํ ํก์
๋ง์ทจ์ ๋ ์๊ถ์
์ถ์ ์ฅ์ ๋ฅผ ์ผ์ผํค๋ฏ๋ก ๋ฌธ์ ์ ๋๊ณ ์๋ค(Munson, 1970: ไปป๋ฑ, 1971: ้, 1972).
์์์ ์ผ๋ก ketamine์ ์๊ถ์์ถ์ ์ด์ง์ํจ๋ค(Chodoff ๋ฐ Stella, 1966: Little๋ฑ, 1
972; Galbert ๋ฐ Gardner, 1973; Corssen 1974)๊ณ ๋ณด๊ณ ๋๋ฐ ์์ผ๋ฉฐ, Jawalekar ๋ฑ(1972)
์ ์ฅ์ ์์ ์๊ถ์ ํธ์ ketamine์ ์ ์ฉํ์ฌ ์๊ถ์ด๋์ ์ด์ง์ ๊ด์ฐฐํ์๋ค. ้(1975)์
์ํ๋ฉด ๊ฐํ ์์ ketamine์ ์๊ถ์ด๋ ์ด์ง์์ฉ์ adrenergic ๋ฐ cholinergic receptor
์ ๊ด๊ณ์์ด ๋์ํธ๋ฅด๋ชฌ์ค ์ฃผ๋ก progesterone์ ์ํฅ์ ๋ฐ์ผ๋ฉฐ ์๊ถ๊ทผ์ ๋ํ์ฌ ์ง์ ์ ์ผ
๋ก ์์ฉํ๋ค๊ณ ํ๋ค.
์ด์ ์ ์๋ ketamine์ด ํด๋ช
(guinea pig)์ ์๊ถ์ ๋ํด์๋ ์ด์ง์์ฉ์ ๋ํ๋ด๋์ง์
์ฌ๋ถ์ ๊ดํด ์ถ๊ตฌํจ๊ณผ ๋์์ ketamine์ด ํด๋ช
์์๋ progesterone์ ์ํฅ์ ๋ฐ๋์ง๋ฅผ
์ถ์ํ๋ค.
์คํ๋๋ฌผ๋ก๋ 0.5ใ๋ด์ธ์ ๋น์์ฑ์์์ฑํด๋ช
(้ๅฆๆ็้ๆงๆตทๆบ)๊ณผ 2.0ใ๋ด์ธ์ ๋น์์ฑ
์์์ฑ๊ฐํ (้ๅงๆ็้ๆงๅฎถใ)์ ์ฌ์ฉํ์๋ค. ํด๋ช
๊ณผ ๊ฐํ ๋ ๊ฐ๊ฐ ์์ธก๋์์ ์ถ 10โผ14์ผ
ํ estrogen์ฃผ์ฌ๊ตฐ์ estradiol benzoate 2,000 I.U./ใ, progesterone์ฃผ์ฌ๊ตฐ์ progeste
rone 5ใ/ใ์ ๋งค์ผ 1ํ 4์ผ๊ฐ ๊ทผ์ก์ฃผ์ฌํ๋ค.
์๊ถ์ ํธ(1.5โผ2.0ใ ๊ธธ์ด)์ ํด๋ช
ํน์ ๊ฐํ ์์ ๋์ดํ๋ ์ฆ์ ๋ถ๋ฆฌ ์ฒ์ถ(ๅๅบ)ํ์ฌ
Locke์ก 50ใ๊ฐ ๋ค์ด์๋ ์ด์ค๋ฒฝ์ด์์ (ไบ้ๅฃ็กๅญ่ฃฝ) muscle chamber ์ ๋ถ(ๅบ้จ)์ ํ๊ณจ
์ ๊ณ ์ ํ๊ณ ๋ค๋ฅธ๋์ lever์ ์ฐ๊ฒฐํ์ฌ ๊ทธ ์์ถ์ kymograph์ง์ ๋ฌ์ฌํ์๋ค. ์ด๋ musc
le chamber๋ด Locke์ก์ 38โ๋ก ์ผ์ ํ๊ฒ ์ ์ง์ํค๊ณ ์ฐ์๋ฅผ ๊ณ์ ๊ณต๊ธํ๋ค. ์๊ถ์ ํธ์
์๋ฐ์ด๋์ด ์ผ์ ํ๊ฒ ๋จ์ ๊ธฐ๋ค๋ ค ketamine์ ์ ์ฉํ๊ณ ์ด๋๊ณก์ ์ ๋ณํ๋ฅผ ๊ด์ฐฐํ์๋๋ฐ
๋ค์๊ณผ ๊ฐ์ ๊ฒฐ๊ณผ๋ฅผ ์ป์๋ค.
1) ํด๋ช
์ ์๊ถ์ด๋์์์ ๊ฐํ ์๋ ๋ฌ๋ฆฌ ๋์ ์์ถ๊ณ ์ ์ ์ ์์ถ๋น๋๋ฅผ ๋ํ๋ด์๋ค.
2) Estrogen์ฃผ์ฌ ํด๋ช
์๊ถ์ ํธ์ 1โผ25 ฮณ/ใ์ ketamine์ ์ ์ฉํ์๋๋ฐ ์๊ถ์ด๋์์
์ ์๋ฌด๋ฐ ๋ณํ๊ฐ ์์๊ณ 50 ฮณ/ใ์ด์์ ๋๋์ ์ ์ฉํ์์ ๋๋ ์คํ๋ ค ์๊ถ์์ถ๊ณ ์
์ ํ๋ฅผ ๋ํ๋ด์๋ค.
3) Progesterone์ฃผ์ฌ ํด๋ช
์๊ถ์ ํธ์ 1โผ100 ฮณ/ใ์ ketamine์ ์ ์ฉํ์๋ ์๋ฌด๋ฐ ๋ฐ
์์ด ์์์ผ๋ estrogenํฌ์ฌ๊ตฐ์ 3๋ฐฐ์ ์์ธ 150 ฮณ/ใ์ ๋๋์์ ์ญ์ ์๊ถ์์ถ๊ณ ์ ์
ํ๋ฅผ ๋ํ๋์ผ๋ฉฐ 200 ฮณ/ใ์ ๋๋์์๋ ํ์ ํ ์ต์ ๋ฅผ ๋ณด์ฌ์ฃผ์๋ค.
4) Estrogen์ฃผ์ฌ ๊ฐํ ์๊ถ์ ํธ์ ๋ํ ๋๋์ ketamine์ ์ํฅ์ 20 ฮณ/ใ์ ๋๋์์
๋ ์๋ฌด ๋ณํ๊ฐ ์์์ผ๋ ํด๋ช
์๊ถ์ ํธ์์ ์์ถ๊ณ ์ ์ ํ๋ฅผ ๋ณด์ฌ์ฃผ๋ 50 ฮณ/ใ์ ๋๋์
์๋ ์ญ์ ์์ถ๊ณ ์ ์ ํ๋ฅผ ๋ํ๋ด์๋ค.
5) Progesterone์ฃผ์ฌ ๊ฐํ ์๊ถ์ ํธ์ ๋ํ ๋๋์ ketamine์ ์ํฅ์ ๋ณด์๋๋ฐ 150 ฮณ/
ใ์ ๋๋์์๋ ์์ถ๊ณ ์ ํญ์ง์ ๋ํ๋์ผ๋ 200 ฮณ/ใ์ ๋๋์์๋ ์ญ์ ์์ถ๊ณ ์ ์
ํ๋ฅผ ๋ํ๋๋ค.
์ด์์ ๊ฒฐ๊ณผ, ketamine์ ์๊ถ์์ถ์์ฉ์ ๊ฐํ ์ ์์ด์๋ progesterone์ ์ํฅ์ ๋ฐ์ผ
๋ ํด๋ช
์ ์์ด์๋ progesterone์ ์ํฅ์ ๋๋ ท์ด ๊ด์ฐฐํ ์๋ ์์๋ค. ์ฆ ์ข
์กฑ์ฐจ์ด๊ฐ
์๋ค๊ณ ์๊ฐํ ์ ์์๋ค. ๊ทธ๋ฆฌ๊ณ ketamine์ ๋๋ ์ ์ฉํ๊ฒ ๋๋ฉด ์๊ถ์์ถ๊ณ ์ ์ต์ ํ์
์ด ๋ํ๋๋๋ฐ ๊ทธ ์ต์ ๋์ ํด๋ช
๋ฐ ๊ฐํ ๋ชจ๋ estrogenํฌ์ฌ๊ตฐ๋ณด๋ค progesteroneํฌ์ฌ๊ตฐ์
์์ด์ ๋ ๋๋์ด ํ์ํจ์ ๋ณผ ์ ์์๋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. 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
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