• Title/Summary/Keyword: Hepatic uptake

검색결과 123건 처리시간 0.027초

간세포암의 $^{99m}Tc-DISIDA$ 신티그램 소견 ([ $^{99m}Tc-DISIDA$ ] Scintigraphic Findings of Hepatocellular Carcinoma)

  • 김성훈;정수교;박용휘
    • 대한핵의학회지
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    • 제20권1호
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    • pp.33-37
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    • 1986
  • It is well known that $^{99m}Tc-sulfur$ colloid or phytate hepatic scintigraphy is highly sensitive but not specific. Both $^{99m}Tc-DISIDA$ and bilirubin have been shown to share the same anionic transport pathway in the liver. Hepatocellular carcinoma(HCC) retains the ability to produce bile but has marked limitation to excreting it resulting in accumulation of bile within the tumor cells. Based upon such a fact, $^{99m}Tc-DISIDA$ hepatobiliary scintigraphy is used for the diagnosis of HCC. The present communication deals with our experience of DISIDA scintigraphic exploration of 9 cases of HCC in a retrospective way. We have made an observation on intensity of positive radio nuclide accumulation in the cold area of HCC as it is demonstrated by phytate scintigraphy. In addition we have semi quantitatively analyzed time-activity pattern and the following results were obtained. (1) All of 9 cases showed an increased uptake of $^{99m}Tc-DISIDA$ in delayed scintigrams. Of these 5 cases showed accumulation less than, 3 equal to, 1 more than the surrounding liver tissue. (2) The mean of the first appearing time of $^{99m}Tc-DISIDA$ activity in tumoral region was 2 hours and 20 minutes. (3) DISIDA scintigraphy provides us with positive informations of diagnostic value.

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원발성간암(肝癌)과 아메바성간농양(肝膿瘍)의 진단에 관한 핵의학(核醫學)적 고찰 (Radiogold Study in Primary Hepatoma and Amebic Liver Abscess: Is Their Distinction Possible?)

  • 박용휘;김동집
    • 대한핵의학회지
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    • 제2권1호
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    • pp.53-58
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    • 1968
  • Both primary hepatoma and amebic liver abscess are probably the most common space-occupying disease of the liver in Korea, and the importance of their accurate distinction can not be overemphasized. Radiogold hepatoscanning has been widely used at St. Mary's Hospital, and recently blood disappearance rate of colloidal $^{198}Au$ has been introduced in the study of hepatic ailments. A review of the literature revealed few previous publications concerning the differential features of the two conditions although some characteristic scan findings of each condition have been described. The present study is aimed at a critical review and analysis of various photoscan findings and blood disappearance rate determinations of colloidal $^{198}Au$ of 34 cases of primary hepatoma and 30 cases of amebic liver abscess. Among many scan manifestations, prominence of the uninvolved liver tissue, "hemispherical cold area," and splenic uptake are much more commonly encountered in primary hepatoma and the blood disappearance rate tends to be far more frequently delayed in primary hepatoma than in abscess providing at least a statistically useful basis of distinction of the two diseases.

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Caffeine attenuates lipid accumulation via activation of AMP-activated protein kinase signaling pathway in HepG2 cells

  • Quan, Hai Yan;Kim, Do Yeon;Chung, Sung Hyun
    • BMB Reports
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    • 제46권4호
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    • pp.207-212
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    • 2013
  • The main purpose of this study is to examine the effect of caffeine on lipid accumulation in human hepatoma HepG2 cells. Significant decreases in the accumulation of hepatic lipids, such as triglyceride (TG), and cholesterol were observed when HepG2 cells were treated with caffeine as indicated. Caffeine decreased the mRNA level of lipogenesis-associated genes (SREBP1c, SREBP2, FAS, SCD1, HMGR and LDLR). In contrast, mRNA level of CD36, which is responsible for lipid uptake and catabolism, was increased. Next, the effect of caffeine on AMP-activated protein kinase (AMPK) signaling pathway was examined. Phosphorylation of AMPK and acetyl-CoA carboxylase were evidently increased when the cells were treated with caffeine as indicated for 24 h. These effects were all reversed in the presence of compound C, an AMPK inhibitor. In summary, these data indicate that caffeine effectively depleted TG and cholesterol levels by inhibition of lipogenesis and stimulation of lipolysis through modulating AMPK-SREBP signaling pathways.

Green tea and type 2 diabetes

  • Park, Jae-Hyung;Bae, Jae-Hoon;Im, Sung-Soon;Song, Dae-Kyu
    • Integrative Medicine Research
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    • 제3권1호
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    • pp.4-10
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    • 2014
  • Green tea and coffee consumption have been widely popular worldwide. These beverages contain caffeine to activate the central nervous system by adenosine receptor blockade, and due to the caffeine, addiction or tolerance may occur. In addition to this caffeine effect, green tea and coffee consumption have always been at the center of discussions about human health, disease, and longevity. In particular, green tea catechins are involved in many biological activities such as antioxidation and modulation of various cellular lipid and proteins. Thus, they are beneficial against degenerative diseases, including obesity, cancer, cardiovascular diseases, and various inflammatory diseases. Some reports also suggest that daily consumption of tea catechins may help in controlling type 2 diabetes. However, other studies have reported that chronic consumption of green tea may result in hepatic failure, neuronal damage, and exacerbation of diabetes, suggesting that interindividual variations in the green tea effect are large. This review will focus on the effect of green tea catechins extracted from the Camellia sinensis plant on type 2 diabetes and obesity, and the possible mechanistic explanation for the experimental results mainly from our laboratory. It is hoped that green tea can be consumed in a suitable manner as a supplement to prevent the development of type 2 diabetes and obesity.

Interleukin-6-producing paraganglioma as a rare cause of systemic inflammatory response syndrome: a case report

  • Yin Young Lee;Seung Min Chung
    • Journal of Yeungnam Medical Science
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    • 제40권4호
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    • pp.435-441
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    • 2023
  • Pheochromocytomas and paragangliomas (PPGLs) may secrete hormones or bioactive neuropeptides such as interleukin-6 (IL-6), which can mask the clinical manifestations of catecholamine hypersecretion. We report the case of a patient with delayed diagnosis of paraganglioma due to the development of IL-6-mediated systemic inflammatory response syndrome (SIRS). A 58-year-old woman presented with dyspnea and flank pain accompanied by SIRS and acute cardiac, kidney, and liver injuries. A left paravertebral mass was incidentally observed on abdominal computed tomography (CT). Biochemical tests revealed increased 24-hour urinary metanephrine (2.12 mg/day), plasma norepinephrine (1,588 pg/mL), plasma normetanephrine (2.27 nmol/L), and IL-6 (16.5 pg/mL) levels. 18F-fluorodeoxyglucose (FDG) positron emission tomography/CT showed increased uptake of FDG in the left paravertebral mass without metastases. The patient was finally diagnosed with functional paraganglioma crisis. The precipitating factor was unclear, but phendimetrazine tartrate, a norepinephrine-dopamine release drug that the patient regularly took, might have stimulated the paraganglioma. The patient's body temperature and blood pressure were well controlled after alpha-blocker administration, and the retroperitoneal mass was surgically resected successfully. After surgery, the patient's inflammatory, cardiac, renal, and hepatic biomarkers and catecholamine levels improved. In conclusion, our report emphasizes the importance of IL-6-producing PPGLs in the differential diagnosis of SIRS.

$K^+$ 통로개방제 Pinacidil이 종양이식 생쥐에서 Tl-201의 체내분포에 미치는 영향 (Effects of Pinacidil, a Potassium-Channel Opener, on Biodistribution of Thallium-201 in Tumor-Bearing Mice)

  • 이재태;천경아;이상우;강도영;안병철;전수한;이규보;하정희
    • 대한핵의학회지
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    • 제34권4호
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    • pp.303-311
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    • 2000
  • 목적: 생체 내에서 potassium과 유사한 역학을 보이는 thallium은 종양의 영상에 널리 사용된다. $K^+$ 통로개방제는 세포 내의 potassium을 외부로 배출되게 하는 기능이 있어 Tl-201을 이용한 종양영상에도 영향을 미칠 수 있을 것이라 생각된다. 본 연구는 강력한 $K^+$ 통로개방제의 하나인 pinacidil이 Tl-201을 이용한 종양의 국소화에 어떠한 영향을 미치는 가를 알아보기 위하여, 종양을 가진 생쥐에서 pinacidil에 의한 Tl-201의 체내분포 변화를 알아보았다. 대상 및 방법: 생쥐 유방암세포주를 이식받은 Balb/c 생쥐를 3주간 사육한 후 실험에 이용하였다. Tl-201 185 KBq를 꼬리정맥을 통해 주입한 후 일정시간에 실험동물을 희생시켜 Tl-201의 체내 분포를 알아 보았으며, pinacidil $100{\mu}g$ 투여에 따른 분포 변화를 알아보았다. 또한 Tl-201 3.7 MBq를 꼬리정맥을 통해 주입하여 Tl-201의 시간에 따른 전신 잔류율을 측정하였고, pinacidil 투여에 의한 전신 잔류율 변화를 구하였다. 결과: pinacidil 투여시 대조군에 비해 혈액 내 Tl-201의 방사능치를 약간 감소시키나 신장에서는 현저한 감소를 일으켰다. 또한 간, 근육, 및 장관의 방사능은 pinacidil 투여에 의해 변하지 않았다. 종양 내 Tl-201 섭취율 및 종양조직/혈액 무게당 섭취비는 대조군에 비해 pinacidil 투여군에서 낮았으며, Tl-201의 24시간 전신 잔류율도 pinacidil 투여군에서 낮았다. 결론: $K^+$ 통로개방제는 Tl-201의 체외 배설을 촉진시키고, 신장 섭취를 감소시켜나, 종양 섭취량도 감소시켰다. 그러므로 Tl-201 종양영상 판독시 $K^+$ 통로개방제를 사용하는 경우에는 오히려 Tl-201 종양영상의 질이 향상되기 보다는 저하될 수 있다는 사실을 고려하여야 할 것으로 생각된다.

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$^{99m}Tc$-MAA를 이용한 간세포암의 간동맥 관류 스캔의 유용성 (Usefulness of Hepatocellular Carcinoma by Hepatic Arterial Perfusion Scintigraphy with $^{99m}Tc$-MAA)

  • 정지욱;이효영;윤종준;이화진;이무석;송현석;박세윤
    • 핵의학기술
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    • 제14권2호
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    • pp.155-158
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    • 2010
  • $^{99m}Tc$-macroaggregated albumin (MAA) 를 이용한 간동맥 관류스캔(hepatic arterial perfusion scintigraphy, HAPS)은 간종양의 경동맥 화학요법을 위해 종양의 관류 등을 평가하는데 매우 유용한 방법으로 알려져 있다. 본 연구는 간암환자(hepatocellular carcinoma, HCC)에서의 정상 간 조직에 대한 간세포암의 상대적인 혈류량을 평가하여 종양의 형태, 크기와 lung shunting, tumor to normal ratio (T/N ratio)를 측정하여 HAPS 의 유용성을 알아보고자 하였다. 2009년 6월부터 2009년 9월까지 본원에서 HCC 진단을 받은 환자 7명(평균 64세, 남자 6명, 여자 1명)을 대상으로 하였다. $^{99m}Tc$-MAA 5 mCi를 간 동맥 내에 위치된 카테타를 통하여 주입하고 20분경과 후 HAPS를 시행하였다. 환자의 흉부와 복부가 포함되게 시야를 잡고 anterior, posterior, both lateral 상을 얻고 SPECT를 시행하였다. liver, tumor, lung의 ROI를 그리고 각각의 count와 count/pixel (mean value) 를 구하여 lung shunting, T/N ratio를 구하였다. anterior, posterior 상에서 얻어진 ROI에서 얻어진 tumor size는 2.0~10.8 cm(평균 3.75 cm), liver size 는 8.8~18.5 cm(평균14.6 cm)였다. total tumor와 total normal의 mean value를 통해 얻은 T/N ratio의 범위는 2.41~5.76(평균 3.8)였다. total lung과 total liver의 counts를 통해 얻은 lung shunting의 범위는 3.14~13.92%(평균 6.77%)였다. $^{99m}Tc$-MAA를 이용한 HAPS 는 정상 간 조직에 비해 간세포암내에 강한 방사능 섭취를 보였으며 종양의 크기, 위치 및 T/N ratio를 통한 정량적 관류 평가를 할 수 있었다. 또한 폐 섭취 빈도는 종양 내 동정맥 단락을 추정할 수 있어 간동맥 동위원소 치료 전 단락 유무를 평가할 수 있다는 점이 유용하게 활용될 수 있을 것이다. 따라서 $^{99m}Tc$-MAA를 이용한 HAPS는 간암의 평가 및 치료를 결정 할 수 있는 유용한 검사법으로 이용될 수 있을 것으로 사료된다.

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Re-188이 표지된 황 교질(Sulfur Colloid)/리피오돌(Lipiodol)의 제조와 생체내 분포 (Preparation and Biodistribution of Re-188-Sulfur Colloid Suspension in Lipiodol)

  • 김영주;정재민;김석기;손미원;이동수;정준기;이명철
    • 대한핵의학회지
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    • 제37권5호
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    • pp.301-307
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    • 2003
  • 목적: 리피오돌은 간암환자의 간동맥으로 투여시 암에 많이 섭취된다. 이 연구에서는 Re-188-황 교질/리피오돌을 제조하여 생체내분포를 보았다. 재료 및 방법: Re-188-황 교질/리피오돌을 마우스의 꼬리정맥으로 주사한후 1 시간 후에 생체내 분포를 확인하였다. 간암을 유발시킨 백서의 좌심실로 Re-188-황 교질/리피오돌을 주사하고 5 분후의 생체내 분포와 간의 자가방사사진을 보았다. 결과: Re-188-황 교질/리피오돌을 마우스의 꼬리정맥으로 주사한 후 1시간(n=3)섭취율(% ID/organ)은 간에서 $5.2{\pm}0.7$, 폐는 $91.0{\pm}1.7$이었다. 간암을 유발시킨 백서의 좌심실로 Re-188-황 교질/리피오돌을 주사한 후 5 분(n=4)의 정상간의 섭취율(% ID/g)은 $0.41{\pm}0.28$, 간암은 $1.88{\pm}1.57$, 폐는 $1.65{\pm}1.54$였으며, 자가방사사진에서도 간암부위의 섭취가 정상적인 간조직 보다 증가되었다. 결론: Re-188-황 교질/리피오돌을 동맥으로 투여시 간암부위의 섭취가 정상적인 간조직보다 많아 간암치료용 방사성의약품으로서 사용할 수 있음을 알았다.

Effects of Curcumin on the Pharmacokinetics of Loratadine in Rats: Possible Role of CYP3A4 and P-glycoprotein Inhibition by Curcumin

  • Li, Cheng;Choi, Byung-Chul;Kim, Dong-Ki;Choi, Jun-Shik
    • Biomolecules & Therapeutics
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    • 제19권3호
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    • pp.364-370
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    • 2011
  • The purpose of this study was to investigate the effects of curcumin on the pharmacokinetics of loratadine in rats. The effect of curcumin on P-glycoprotein (P-gp) and cytochrome P450 (CYP) 3A4 activity was evaluated. Pharmacokinetic parameters of loratadine were also determined after oral and intravenous administration in the presence or absence of curcumin. Curcumin inhibited CYP3A4 activity with an IC50 value of 2.71 ${\mu}M$ and the relative cellular uptake of rhodamine-123 was comparable. Compared to the oral control group, curcumin significantly increased the area under the plasma concentration-time curve and the peak plasma concentration by 39.4-66.7% and 34.2-61.5%. Curcumin also significantly increased the absolute bioavailability of loratadine by 40.0-66.1% compared to the oral control group. Consequently, the relative bioavailability of loratadine was increased by 1.39- to 1.67-fold. In contrast, curcumin had no effect on any pharmacokinetic parameters of loratadine given intravenously, implying that the enhanced oral bioavailability may be mainly due to increased intestinal absorption caused via P-gp and CYP3A4 inhibition by curcumin rather than to reduced renal and hepatic elimination of loratadine. Curcumin enhanced the oral bioavailability of loratadine in this study. The enhanced bioavailability of loratadine might be mainly attributed to enhanced absorption in the gastrointestinal tract via the inhibition of P-gp and reduced fi rst-pass metabolism of loratadine via the inhibition of the CYP3A subfamily in the small intestine and/or in the liver by curcumin.

췌장 선방세포암 1예 (A Case of Pancreatic Acinar Cell Carcinoma)

  • 이화정;지준호;박승찬;박정철;최은정;서혜진;이원식;이정림;배병조;손경락;이경희
    • Journal of Yeungnam Medical Science
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    • 제25권2호
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    • pp.128-133
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    • 2008
  • Acinar cell carcinoma is a rare tumor that represents 1~2% of all pancreatic cancers. Clinical and radiologic findings are inconclusive in this disease. Acinar cell carcinoma is characterized by rapid progression and early metastasis, which lead to its poor prognosis. A 41-year-old man was admitted to our hospital for abdominal pain. Abdominal computed tomography (CT) and positron emission tomography-computed tomography (PET-CT) showed a splenic mass, which was being invaded by a pancreatic tail mass and which had increased $^{18}F$-fluorodeoxyglucose (FDG) uptake. Primary radical distal pancreatectomy and splenectomy were performed. Pathologic findings revealed an acinar cell carcinoma of the pancreas. The patient underwent a total gastrectomy three months later because of gastric recurrence. Four months later, multiple hepatic metastases were discovered, and the patient underwent a left hepatectomy. During treatment with capecitabine, there was no evidence of tumor progression for 14 months. We report a case of metastatic pancreatic acinar cell carcinoma, which did not progress for an extended period while the patient was being treated with capecitabine.

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