• Parasites, Hosts and Diseases
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• 제53권3호
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• pp.271-277
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• 2015

The genetic diversity of Schistosoma haematobium remains largely unstudied in comparison to that of Schistosoma mansoni. To characterize the extent of genetic diversity in S. haematobium among its definitive host (humans), we collected S. haematobium eggs from the urine of 73 infected schoolchildren at 5 primary schools in White Nile State, Sudan, and then performed a randomly amplified polymorphic DNA marker ITS2 by PCR-RFLP analysis. Among 73 S. haematobium egg-positive cases, 13 were selected based on the presence of the S. haematobium satellite markers A4 and B2 in their genomic DNA, and used for RFLP analysis. The 13 samples were subjected to an RFLP analysis of the S. haematobium ITS2 region; however, there was no variation in size among the fragments. Compared to the ITS2 sequences obtained for S. haematobium from Kenya, the nucleotide sequences of the ITS2 regions of S. haematobium from 4 areas in Sudan were consistent with those from Kenya (> 99%). In this study, we demonstrate for the first time that most of the S. haematobium population in Sudan consists of a pan-African S. haematobium genotype; however, we also report the discovery of Kenyan strain inflow into White Nile, Sudan.

• 약학회지
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• 제42권6호
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• pp.576-582
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• 1998

Fenfluramine, an anorectic agent, is widely abused as a diet pill in Korea because it is freely marketed in China without any regulation. The optical isomers of fenfluramine hav e different phamacological actions: d-form is used as an anorectic agent, while l-form as a neuroleptic agent. To investigate the metabolism when racemic fenfluramine was administered orally, the urinary excretion of fenfluramine was studied in rats. The enantiomeric separation of fenfluramine was performed on achiral column by gas chromatography using (S)-N-(trifluoroacetyl)-l-prolyl chloride (TFP) as a derivatizing agent. After administration of 15mg/kg of racemic fenfluramine to rats, d-, l-fenfluramine and its metabolites d- and l norfenfluramine in urine were determined by chromatographic separation of TFP derivatives on DB-1 at retention time of 11.2, 11.8, 8.4 and 8.6 min respectively. Urinary recoveries of d and l-fenfluramine in rat were 0.42-5.9O% and 0.18-1.20% respectively in urine specimens collected during first 24hr. The comparison in the levels of isomers showed that d- fenfluramine were higher than l-form, while d-norfenfluramine were lower than l-form. The ratios between parent compound and metabolite revealed that d-norfenfluramine to d-fenfluramine ranged from 1.0 to 4.4, while the ratio of l-norfenfluramine to l-fenfluramine was 8.2-21.1 indicating that l-fenfluramine is metabolized faster than the d-isomer.

• 혜화의학회지
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• 제10권1호
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• pp.157-166
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• 2001

Oryoungsan which first recorded in Sanghanron, the clinical medical book consists of treating acute febrile disease according to its change, is one of the frequently used oriental medicines. these days, it has been prescribed in symptoms accompanied by edema mostly. therefore it is easy to consider it as a type of diuretics. In Sanghanron it was originally used in the symptoms of perspiration, decreased urine volume, thirsty, flatulence. these symptoms indicate loss of body fluid and the prescription which orders "taking warm water sufficiently" supports this. On this background, it is supposed that Oryoungsan treats dehydration after providing water and electrolytes. To consider that herbal medicines consisted of Oryoungsan make electrolytes go out of the body, The healing mechanism of dehydration doesn't meet this. Because Oryoungsan was used in condition of fever or in similar condition, it is more resonable to understand that restoration of increasing blood flow to the subcutaneous venous plexus regulating body temperature in febrile condition into body circulation, resulting into maintaining main blood volume and into treating decreased urine volume and thirsty is Oryoungsan's function in the dehydration or febrile condition. That is, symptoms are decreased or disappeared through restoring unbalance of internal body fluid. The other target is pain controls, especially chronic headache, facial pain and trigeminal neuralgia. it is suggested that the function of pain control of Oryoungsan is related to 5-HT(5-hydroxytrypamine), nerve transmitter in the endogenous analgesic system. Moreover it is also suggested that Oryoungsan is relate to 5-HT, considering the fact that gastroparesis, a symptom of cyclic vomiting syndrome treated with 5-HT1D receptor agonist is similar to the 'bi', symptoms appeared in the Oryoungsan-related disease.

• Archives of Pharmacal Research
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• 제27권2호
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• pp.265-272
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• 2004

The pharmacokinetics of CKD-732 (6-0-4-[dimethyl-aminoethoxy)cinnamoyl]-fumagillolㆍhemioxalate) was investigated in male SD rats and beagle dogs after bolus intravenous administration. The parent compound and metabolites obtained from in vitro and in vivo samples were determined by LC/MS. The main metabolite was isolated and identified as an N-oxide form of CKD-732 by NMR and LC/MS/MS. CKD-732 was metabolized into either M11 or others by rapid hydroxylation, demethylation, and hydrolysis. The blood level following the intravenous route declined in first-order kinetics with $T_{1}$2/$\beta$ values of 0.72-0.78 h for CKD-732 and 0.92-1.09 h for M11 in rats at a dose of 7.5-30 mg/kg. In dogs, $T_{1}$2/$\beta$ values of CKD-732 and M11 were 1.54 and 1.79 h, respectively. Moreover, AUC values increased dose dependently for CKD-732 and M11 in rats and dogs. The CLtot and Vdss did not change significantly with increasing dose, indicating linear pharmacokinetic patterns. The excretion patterns through the urine, bile, and feces were also examined in the animals. The total amount excreted in urine, bile, and feces was 2.13% for CKD-732 and 1.29% for M11 in rats, and 1.58% for CKD-732 and 2.28% for M11 in dogs.

• Journal of Ginseng Research
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• 제45권5호
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• pp.565-574
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• 2021

Background: Saengmaeksan (SMS) is a traditional Korean medicine composed of three herbs, Panax ginseng, Schisandra chinensis, and Liriope platyphylla. SMS is used to treat respiratory and cardiovascular disorders. However, whether SMS exerts antihyperuricemic effects is unknown. Methods: Effects of the SMS extract in water (SMS-W) and 30% ethanol (SMS-E) were studied in a rat model of potassium oxonate-induced hyperuricemia. Uric acid concentrations and xanthine oxidase (XO) activities were evaluated in the serum, urine, and hepatic tissue. Using renal histopathology to assess kidney function and uric acid excretion, we investigated serum creatinine and blood urea nitrogen concentrations, as well as protein levels of renal urate transporter 1 (URAT1), glucose transporter 9 (GLUT9), and organic anion transporter 1 (OAT1). The effects of SMS on in vitro XO activity and uric acid uptake were also evaluated. The components of SMS were identified using Ultra Performance Liquid Chromatography (UPLC). Results: SMS-E reduced serum uric acid and creatinine concentrations, and elevated urine uric acid excretion. SMS-E lowered XO activities in both the serum and liver, and downregulated the expression of renal URAT1 and GLUT9 proteins. SMS-E reduced renal inflammation and IL-1b levels in both the serum and kidneys. SMS-E inhibited both in vitro XO activity and urate uptake in URAT1-expressing oocytes. Using UPLC, 25 ginsenosides were identified, all of which were present in higher levels in SMS-E than in SMS-W. Conclusion: SMS-E exhibited antihyperuricemic effects by regulating XO activity and renal urate transporters, providing the first evidence of its applicability in the treatment of hyperuricemia and gout.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제22권5호
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• pp.453-459
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• 2019

Purpose: Jaundice accounts for most hospital admissions in the neonatal period. Nowadays, in addition to phototherapy, other auxiliary methods are used to reduce jaundice and the length of hospitalization. This study aimed to investigate the effect of probiotics on the treatment of hyper-bilirubinemia in full-term neonates. Methods: In this randomized clinical trial, 83 full-term neonates, who were admitted to the hospital to receive phototherapy in the first 6 months of 2015, were randomly divided into two groups: synbiotic (SG, n=40) and control (CG, n=43). Both groups received phototherapy but the SG also received 5 drops/day of synbiotics. Serum bilirubin, urine, stool, feeding frequency, and weight were measured daily until hospital discharge. A p-value<0.05 was considered statistically significant. Results: The mean total serum bilirubin in the SG was lower than that in the CG ($9.38{\pm}2.37$ and $11.17{\pm}2.60mg/dL$, respectively). The urine and stool frequency in the SG was significantly higher than that in the CG (p<0.05). The duration of hospitalization in the SG was shorter than that in the CG. Conclusion: Use of synbiotics as an adjuvant therapy had a significant treatment effect on jaundice in full-term neonates. Further studies including larger samples with long follow-up periods are essential to confirm the benefits of routine use of synbiotics in neonatal patients with jaundice.

• Journal of Trauma and Injury
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• 제34권4호
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• pp.299-304
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• 2021

Atypical hemolytic uremic syndrome (aHUS) is a rare, progressive, life-threatening condition of thrombotic microangiopathy characterized by thrombocytopenia, microangiopathic hemolytic anemia, and renal impairment. The mechanisms underlying aHUS remain unclear. Herein, we present the first case in the literature of aHUS after a traumatic injury. A 55-year-old male visited the emergency department after a traumatic injury caused by a tree limb. Abdominal computed tomography revealed a rectal wall defect with significant air density in the perirectal space and preperitoneum, implying rectal perforation. Due to the absence of intraperitoneal intestinal perforation, we performed diverting sigmoid loop colostomy. An additional intermittent simple repair was performed due to perianal and anal injuries. One day postoperatively, his urine output abruptly decreased and serum creatinine level increased. His platelet level decreased, and a spiking fever occurred after 2 days. The patient was diagnosed with acute renal failure secondary to aHUS and was treated with fresh frozen plasma replacement. Continuous renal replacement therapy (CRRT) was also started for oliguria and uremic symptoms. The patient received CRRT for 3 days and intermittent hemodialysis thereafter. After hemodialysis and subsequent supportive treatment, his urine output and renal function improved. The hemolytic anemia and thrombocytopenia also gradually improved. Dialysis was terminated on day 22 of admission and the patient was discharged after recovery. This case suggests that that a traumatic event can trigger aHUS, which should be considered in patients who have thrombocytopenia and acute renal failure with microangiopathic hemolytic anemia. Early diagnosis and appropriate management are critical for favorable outcomes.

• Childhood Kidney Diseases
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• 제4권1호
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• pp.69-76
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• 2000

목 적 : 일차성 야뇨증의 병인론은 유전적 요인 외에 수면 요인, 야간 Arginine Vasopressin(AVP)분비 장애, 기능적 방광 미숙 등 주로 배뇨 반사의 성숙 지연이 논의되고 있으나 위험 요인에 대한 연구는 적었다. 이에 저자들은 소변을 충분히 가릴 나이인 5세 이후까지 야뇨증을 지속시킬 수 있는 위험 요인들을 분석하고자 하였다. 대상 및 방법 ;서울 목동지역 초등학교 1학년의 정기 신체 검사에서 야뇨증 설문지 조사를 통해 일차성 야뇨증으로 확인된 아동 20명과 이후 1년간 이화여자대학교 목동병원 소아과 외래에서 동일한 설문지 조사를 받은 6-7세의 일차성 야뇨증 아동 35명을 포함한 55명을 야뇨증군으로 하였고, 설문지 조사에서 야뇨증이 없었던 아동 221명을 대조군으로 하였다. 이중 야뇨증군 55명과 대조군 22명에서는 24시간 배뇨 일지를 기록하게 하였으며, 두 군사이에 유전적 요인, 심리적 요인, 발달 요인, 수면 요인, 일일 및 야간 수분 섭취량과 요량, 주간 배뇨 장애 및 일회 최대 요량 등을 비교분석 하였다. 결 과 : 1)부모의 야뇨증 병력은 야뇨증군에서 $20.0\%$로 대조군의 $2.7\%$에 비해 유의하게 많았다(P<0.05). 남녀비는 야뇨증군과 대조군에서 유의한 차이가 없었다. 2)출생 순서, 어머니의 직장 여부, 아동과 부모의 성격, 걷기 시작한 나이 및 학교 성적 두 군간에 유의한 차이가 없었다. 3) 잠에서 깨어나기 힘든 경우는 야뇨증군에서 $70.9\%$로 대조군의 $54.3\%$에 비해 유의하게 많았으나(P<0.05), 수면 시간은 차이가 없었다. 4) 야간 수분 섭취량은 야뇨증군에서 $330{\pm}158.2\;mL$로 대조군의 $235{\pm}129.5\;mL$에 비해 유의하게 많았고(P<0.05), 야간 요량은 야뇨증군에서 $390{\pm}61.5mL$로 대조군의 $140{\pm}43.2mL$에 비해 유의하게 많았다(P<0.05). 일일 수분 섭취량과 일일 요량은 두 군간에 유의한 차이가 없었다. 5) 일회 최대 요량은 야뇨증군에서 $107{\pm}35.9mL$로 대조군의 $236{\pm}41.3mL$에 비해 유의하게 적었다((P<0.05). 주간 배뇨 이상은 야뇨증군에서 $80.0\%$로 대조군의 $57.9\%$에 비해 유의하게 많았으며 주간 배뇨 횟수도 야뇨증군에서 $7.0{\pm}3.4$회로 대조군의 $5.4{\pm}1.6$회에 비해 유의하게 많았다(P<0.05). 결 론 :야뇨증은 유전적 요인을 비롯하여 성숙 지연과 관련된 수면 요인, 야간 다뇨, 방광 미숙 등이 관련될 것으로 생각된다. 야간 다뇨의 원인으로 야간 수분 섭취 과다가 관련되므로 치료의 일차 단계로 야간 수분 섭취 제한의 중요성이 강조되어야 한다고 생각된다.

• Clinical and Experimental Pediatrics
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• 제48권4호
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• pp.411-415
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• 2005

목 적 : 방광의 발달과정은 척수배뇨반사에서 척수연수척수반사로의 전환을 특징으로 한다고 알려져 왔다. 향신경인자가 이러한 방광의 발달과정에 관여한다는 동물연구에도 불구하고 인간의 방광 발달과정에도 향신경인자가 역할을 하는지에 관한 연구는 없는 실정이다. 본 연구는 인간의 방광 발달과정에 향신경인자가 관여할 것이라는 가정 하에 방광 발달과정에서 소변의 nerve growth factor(NGF) 변화를 관찰하였다. 방 법 : 배뇨생식기의 선천적 이상을 동반하지 않고 배뇨이상, 요로감염의 증거가 없는 지원자 60명을 대상으로 하였다. 지원자는 출생 후 한달 미만의 신생아, 1년 미만의 유아, 1세, 2세, 3세, 4세의 소아로 분류하였고 각각 10명씩 소변을 채취하였다. 소변의 NGF의 정량은 ELISA 방법을 이용하였고 소아의 연령, 요자제 유무에 따른 NGF의 변화를 NGF/Cr, NGF/total protein 값으로 비교하였다. 결 과 : 연령별로 NGF/Cr은 신생아에서 증가하였다가 유아에 감소하고 1세, 2세에 증가하였다가 3세 때부터 감소하였다. 신생아에서 다른 군과 비교하였을 때 의미있는 증가가 관찰이 되었고(P<0.05) 다른 군에서는 의미있는 차이를 보이지는 않았다. NGF/total protein도 NGF/Cr과 비슷한 양상으로 관찰이 되었다. 자발적 배뇨조절이 가능한 소아는 1세에 2명, 2세에 8명, 3세와 4세에는 10명씩이었다. 1세 이상에서 요자제 유무에 따른 NGF/Cr을 비교하였을 때 요자제가 있는 소아에서 의미있게 감소하였다(P<0.05). 결 론 : 단절배뇨와 높은 방광압력을 특징으로 하는 요자제 이전에 NGF가 증가하였다가 요자제 이후에는 감소하는 것을 확인하였다. 이는 배뇨근-괄약근 협동장애로 인해 증가된 방광조직의 NGF가 역행성 축삭수송을 통해 중추신경계에서 척수반사를 척수연수척수반사로 성숙시키고 이것이 다시 배뇨근-괄약근 성숙을 통해 요자제를 형성하였다고 추정할 수 있다. 이는 인간의 방광 발달과정에도 향신경인자가 방광신경 성장과 배뇨반사의 재구성에 관여함을 시사한다고 생각한다.

• Journal of Nutrition and Health
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• 제34권4호
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• pp.440-448
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• 2001

As diverse physiological functions of taurine have been reported, taurine-containing health drinks and products are marketed worldwide for the treatment of various conditions such as improvements of liver, heart and circulatory functions or as an aid to athletic performance. Although animal studies have shown that taurine is fairly safe when supplemented in the diet for an extended period, the effective dose range of taurine for dietary supplements is in controversy. Reports on dietary taurine intakes have been sparse, and would serve as a guideline for determining an appropriate taurine dosage. The present study was aimed to estimate dietary intake level of taurine using the taurine content database of commonly used food stuffs established recently in our laboratory, and also to evaluate plasma concentration and urinary excretion of taurine in adolescents and adults residing in Seoul area. Dietary taurine intakes of the subjects were 219$\pm$16.9mg/day for 16-19 years old(n=123), 177$\pm$18.1mg/day for adults older than 20 years old(n=123). Male subjects(n=115) consumed 216$\pm$21.1mg of taurine/day, while female subjects(n=131) consumed 181$\pm$14.3mg of taurine/day(p<0.05). The level of dietary taurine intake was positively correlated with the levels of dietary intakes of energy, carbohydrate, total lipids, cholesterol, vitamin A, vitamin B$_1$, niacin, vitamin C, calcium, phosphorous, sodium and potassium at p<0.01, and with dietary intakes of iron and animal lipids at p<0.05, respectively. Plasma taurine concentration of subjects were 135$\pm$5.9$\mu$mol/L, which is considered to be within a normal range for healthy subjects. The subjects excreted 1158$\pm$72.7nmol/ of tarine mg creatinine in their urine, which is approximated as 150-170mg of taurine/24hr urine based on the assumption that 18mg creatinine/kg/day is excreted in the urine of healthy adults, and this would be about 80% of the daily taurine intake observed in the same subjects. Dietary taurine intake level was positively correlated with plasma taurine concentration, as well as with urinary taurine excretion corrected by creatinine excretion at p<0.05. The present study was the first report of taurine intake, and plasma concentration and urinary excretion of taurine in a Korean population so far, and these results would serve as an index for the future study evaluating taurine status in a diverse population within and outside Korea. (Korean J Nutrition 34(4) : 440~448, 2001)