• Journal of Korean Medical Science
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• 제33권51호
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• pp.325.1-325.10
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• 2018

Background: To evaluate survival outcomes and prognostic factors for overall survival (OS) in patients with metastatic renal cell carcinoma (mRCC) who received sunitinib (SU) and pazopanib (PZ) as first-line therapy in real-world Korean clinical practice. Methods: Data of 554 patients with mRCC who received SU or PZ at eight institutions between 2012 and 2016 were retrospectively reviewed. Based on the targeted therapy, the patients were divided into SU (n = 293) or PZ (n = 261) groups, and the clinicopathological variables and survival rates of the two groups were compared. A multivariable Cox proportional hazard model was used to determine the prognostic factors for OS. Results: The median follow-up was 16.4 months (interquartile range, 8.3-31.3). Patients in the PZ group were older, and no significant difference was observed in the performance status (PS) between the two groups. In the SU group, the dose reduction rate was higher and the incidence of grade 3 toxicity was more frequent. The objective response rates were comparable between the two groups (SU, 32.1% vs. PZ, 36.4%). OS did not differ significantly between the two groups (SU, 36.5 months vs. PZ, 40.2 months; log-rank, P = 0.955). Body mass index, Eastern Cooperative Oncology Group PS > 2, synchronous metastasis, poor Heng risk criteria, and liver and bone metastases were associated with a shorter OS. Conclusion: Our real-world data of Korean patients with mRCC suggested that SU and PZ had similar efficacies as first-line therapy for mRCC. However, PZ was better tolerated than SU in Korean patients.

• Clinical and Experimental Reproductive Medicine
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• 제32권2호
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• pp.155-164
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• 2005

Objective: This study was performed to investigate the effects of pioglitazone, an insulin sensitizing agent, on insulin resistance, ovarian function and intraovarian stromal blood flow in patients with polycystic ovarian syndrome (PCOS). Material and Methods: Thirty patients with PCOS, aged 18~34 years, were recruited. Criteria for diagnosis of PCOS were as defined in 2003 Rotterdam consensus. They were treated for 6 months with pioglitazone at a dose of 30 mg/day orally. The hormonal blood profile, fasting serum glucose levels, a glycemic response to 75 g oral glucose tolerance test (OGTT), and an ovarian stromal artery (OSA) blood flow were assessed at baseline and after 6 months of treatment. Results: Eighteen (60.0%) of 30 patients treated with pioglitazone demonstrated a spontaneous ovulation After pioglitazone treatment, fasting insulin concentrations, serum glucose levels after 75 g OGTT significantly decreased (p=0.001, p=0.04, respectively), and fasting glucose to insulin (G/I) ratio significantly increased (p<0.001). The pioglitazone treatment induced a significant reduction in serum LH, testosterone (T) and free T levels (p<0.001, p=0.02, p=0.002, respectively). The resistance index (RI) values of OSA significantly increased after treatment (p<0.001). In analyzing pioglitazone-treated patients according to their body mass index (BMI), nonobese group as well as obese group showed a significant improvement in fasting G/I ratio (p<0.01). The pioglitazone treatment induced a significant reduction in serum LH and free T levels in nonobese group (p<0.001, p<0.05, respectively) as well as obese group (p=0.001, p<0.05, respectively). The RI values of OSA significantly increased in both nonobese and obese groups after pioglitazone treatment (p<0.001, p=0.003, respectively). Conclusions: Pioglitazone could ameliorate the glycoinsulinemic metabolism, and this beneficial effects of this drug could improve the endocrine-reproductive condition associated with the decrease of ovarian stromal artery blood flow, in both nonobese and obese patients with PCOS.

• 한국식품과학회지
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• 제53권5호
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• pp.657-668
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• 2021

본 연구는 일반우유와 무지방우유에서 장출혈성 대장균과 캠필로박터 제주니의 행동예측모델을 개발하고, 미생물학적 안전관리를 위한 기준의 적절성 평가를 위해 정량적 위해성평가를 수행하였다. 시중 마트에서 유통 판매되고 있는 일반우유(n=195)에서 장출혈성 대장균과 캠필로박터 제주니의 오염실태를 모니터링한 결과 모든 제품에서 장출혈성 대장균과 캠필로박터 제주니는 검출되지 않아 초기 오염도는 각각 -3.94 log CFU/mL로 동일하게 추정되었다. 장출혈성 대장균은 7℃ 이상의 온도에서 성장하였고, 캠필로박터 제주니는 4-25℃ 온도의 우유에서 사멸하였다. 우유에서 1차 모델에서 얻은 parameter를 사용하여 장 출혈성 대장균은 2차 성장모델을 캠필로박터 제주니는 2차 사멸예측모델을 개발하였다. 일반우유의 섭취패턴은 식품의약품안전처(2015) 연구에서 수행한 "50대 주요 축산식품의 섭취량 및 섭취패턴조사" 결과를 바탕으로 @RISK 프로그램을 활용하여 하루에 일반우유의 1회 섭취를 통하여 장출혈성 대장균과 캠필로박터 제주니에 의한 식중독 발생 확률을 추정하였다. 추정 결과 1일 1회 일반우유 섭취로 장출혈성 대장균과 캠필로박터 제주니로 인한 평균 식중독 발생 확률은 각각 5.70×10^-5, 9.86×10^-9 것으로 확인되었다. 본 연구에서 정량적 위해평가를 통해 일반우유에서 장출혈성 대장균과 캠필로박터 제주니의 위해수준을 산출한 결과 일반우유에서 장출혈성 대장균의 식중독 발생 가능성이 상대적으로 높으므로 우선관리 대상임을 알 수 있었고, 우유제조업체에서 교차오염 방지, 살균온도/시간 관리, 유통온도, 가정에서 온도 관리 등이 매우 중요할 것으로 사료된다.

• Laboraroty Animal Research
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• 제33권2호
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• pp.57-67
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• 2017

The inhibitory effects of Asparagus cochinchinensis against inflammatory response induced by lipopolysaccharide (LPS), substance P and phthalic anhydride (PA) treatment were recently reported for some cell lines and animal models. To evaluate the hepatotoxicity and nephrotoxicity of A. cochinchinensis toward the livers and kidneys of ICR mice, alterations in related markers including body weight, organ weight, urine composition, liver pathology and kidney pathology were analyzed in male and female ICR mice after oral administration of 150, 300 and 600 mg/kg body weight/day saponin-enriched extract of A. cochinchinensis (SEAC) for 14 days. The saponin, total flavonoid and total phenol levels were found to be 57.2, 88.5 and 102.1 mg/g in SEAC, respectively, and the scavenging activity of SEAC gradually increased in a dose-dependent manner. Moreover, body and organ weight, clinical phenotypes, urine parameters and mice mortality did not differ between the vehicle and SEAC treated group. Furthermore, no significant alterations were measured in alkaline phosphatase (ALP), alanine aminotransferase (ALT), aspartate aminotransferase (AST), lactate dehydrogenase (LDH), blood urea nitrogen (BUN) and the serum creatinine (Cr) in the SEAC treated group relative to the vehicle treated group. Moreover, the specific pathological features induced by most toxic compounds were not observed upon liver and kidney histological analysis. Overall, the results of the present study suggest that SEAC does not induce any specific toxicity in the livers and kidneys of male and female ICR mice at doses of 600 mg/kg body weight/day.

• 생명과학회지
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• 제29권7호
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• pp.785-791
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• 2019

본 연구에서는 편백나무(Chamaecyparis obtusa) 추출액의 항산화 활성 및 항균활성을 검토하였다. 편백나무 추출액의 항산화 활성을 평가하기 위하여 DPPH radical 소거능, ABTS radical 소거능 및 SOD 유사 활성을 분석하였다. 그 결과, 편백나무 추출액의 DPPH radical 및 ABTS radical 소거 활성은 농도 의존적으로 증가하였으며, $50{\mu}l/ml$ 농도에서 78% 및 62%의 최대 활성을 나타내었다. 또한, 편백나무 추출액은 높은 SOD 유사 활성을 보였으며, $50{\mu}l/ml$ 농도에서 92.85 %의 최대 활성을 나타내었다. 한편, 편백나무 추출액의 항균 활성을 측정하기 위해 Paper disc agar diffusion 법을 이용하여 식중독 및 질병을 일으키는 6종의 균주에 대하여 검토하였다. 편백나무 추출액은 B. cereus, E. coli, L. monocytogenes, S. aureus, S. typhi, V. parahaemolyticus에 대한 항균 활성이 나타났고, 이중 B. cereus에 대하여 가장 강한 항 박테리아 활성을 보였다. 이상과 같이 항균 활성이 나타난 6종의 균주에서 편백나무 추출액의 MIC 및 MBC는 $30{\sim}40{\mu}l/ml$로 확인되었다. 이러한 결과는 편백나무 추출액을 이용하여 식중독과 같은 병원균의 성장을 억제하는 항균 소재로 개발한다면 산업적 가치가 높을 것으로 생각된다.

• Asian-Australasian Journal of Animal Sciences
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• 제32권12호
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• pp.1942-1949
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• 2019

Objective: Leukocyte cell-derived chemotaxin 2 (LECT2) is associated with several physiological processes including inflammation, tumorigenesis, and natural killer T cell generation. Chicken LECT2 (chLECT2) gene was originally identified as one of the differentially expressed genes in chicken kidney tissue, where the chickens were fed with different calcium doses. In this study, the molecular characteristics and gene expression of chLECT2 were analyzed under the stimulation of toll-like receptor 3 (TLR3) ligand to understand the involvement of chLECT2 expression in chicken metabolic disorders. Methods: Amino acid sequence of LECT2 proteins from various species including fowl, fish, and mammal were retrieved from the Ensembl database and subjected to Insilco analyses. In addition, the time- and dose-dependent expression of chLECT2 was examined in DF-1 cells which were stimulated with polyinosinic:polycytidylic acid (poly [I:C]), a TLR3 ligand. Further, to explore the transcription factors required for the transcription of chLECT2, DF-1 cells were treated with poly (I:C) in the presence or absence of the nuclear factor ${\kappa}B$ ($NF{\kappa}B$) and activated protein 1 (AP-1) inhibitors. Results: The amino acid sequence prediction of chLECT2 protein revealed that along with duck LECT2 (duLECT2), it has unique signal peptide different from other vertebrate orthologs, and only chLECT2 and duLECT2 have an additional 157 and 161 amino acids on their carboxyl terminus, respectively. Phylogenetic analysis suggested that chLECT2 is evolved from a common ancestor along with the actinopterygii hence, more closely related than to the mammals. Our quantitative polymerase chain reaction results showed that, the expression of chLECT2 was up-regulated significantly in DF-1 cells under the stimulation of poly (I:C) (p<0.05). However, in the presence of $NF{\kappa}B$ or AP-1 inhibitors, the expression of chLECT2 is suppressed suggesting that both $NF{\kappa}B$ and AP-1 transcription factors are required for the induction of chLECT2 expression. Conclusion: The present results suggest that chLECT2 gene might be a target gene of TLR3 signaling. For the future, the expression pattern or molecular mechanism of chLECT2 under stimulation of other innate immune receptors shall be studied. The protein function of chLECT2 will be more clearly understood if further investigation about the mechanism of LECT2 in TLR pathways is conducted.

• 생명과학회지
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• 제31권2호
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• pp.192-198
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• 2021

홍국은 동아시아 국가에서 예로부터 음식과 전통의학에 이용되어 왔다. 홍국은 특정 미생물(일반적으로 Monascus purpureus)이 쌀을 발효시켜 생산되어진다. Monascus sp.는 2차 대사과정을 통해 Monascus 색소, monacolins, γ-aminobutyric acid 등을 생산할 수 있다. Monascus 종의 대사산물인 monacolin K, γ-aminobutyric acid와 dimerumic acid 및 monascus pigments는 항산화 효과, 콜레스테롤과 혈압과 항비만 효과들이 알려져 있다. 본 연구에서는 Monascus sp.로 발효된 홍맥 에탄올 추출물의 항비만 활성을 알아보고자 지방 세포를 이용하여 실험을 실시하였다. 홍국 에탄올 추출물의 항비만 효과는 MDI로 유도된 3T3-L1 전지방세포의 Oil Red O staining과 Real time RT-PCR을 이용하여 비만 유전자 발현을 통해 확인하였다. 홍맥 추출물을 3T3-L1 전지방세포에 각각 200 ㎍/ml, 400 ㎍/ml, 800 ㎍/ml을 처리한 결과 5.04%, 12.24%, 23.52%로 지방축적을 감소시키는 것을 확인하였다. 또한, 홍맥 추출물은 3T3-L1 전지방세포로부터의 C/EBPα, SREBP-1, PPAR-γ 유전자의 발현이 농도 의존적으로 감소되는 것을 확인하였다. 본 연구를 통해 홍맥 추출물의 지방 합성 억제활성을 확인하였으며, 향후 항비만 기능성 식품소재로 활용될 수 있을 것으로 사료된다.

• Molecules and Cells
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• 제44권1호
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• pp.38-49
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• 2021

Airway mucus secretion is an essential innate immune response for host protection. However, overproduction and hypersecretion of mucus, mainly composed of the gel-forming MUC5AC protein, are significant risk factors for patients with asthma and chronic obstructive pulmonary disease (COPD). The transforming growth factor β (TGFβ) signaling pathway negatively regulates MUC5AC expression; however, the underlying molecular mechanism is not fully understood. Here, we showed that TGFβ significantly reduces the expression of MUC5AC mRNA and its protein in NCI-H292 cells, a human mucoepidermoid carcinoma cell line. This reduced MUC5AC expression was restored by a TGFβ receptor inhibitor (SB431542), but not by the inhibition of NF-κB (BAY11-7082 or Triptolide) or PI3K (LY294002) activities. TGFβ-activated Smad3 dose-dependently bound to MUC5AC promoter. Notably, TGFβ-activated Smad3 recruited HDAC2 and facilitated nuclear translocation of HDAC2, thereby inducing the deacetylation of NF-κB at K310, which is essential for a reduction in NF-κB transcriptional activity. Both TGFβ-induced nuclear translocation of Smad3/HDAC2 and deacetylation of NF-κB at K310 were suppressed by a Smad3 inhibitor (SIS3). These results suggest that the TGFβ-activated Smad3/HDAC2 complex is an essential negative regulator for MUC5AC expression and an epigenetic regulator for NF-κB acetylation. Therefore, these results collectively suggest that modulation of the TGFβ1/Smad3/HDAC2/NF-κB pathway axis can be a promising way to improve lung function as a treatment strategy for asthma and COPD.

• The Korean Journal of Pain
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• 제34권1호
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• pp.58-65
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• 2021

Background: Supraspinal delivery of neurotensin (NTS), which may contribute to the effect of a systemically administered agonist, has been reported to be either pronociceptive or antinociceptive. Here, we evaluated the effects of systemically administered NTSR1 agonist in a rat model of neuropathic pain and elucidated the underlying supraspinal mechanism. Methods: Neuropathic pain was induced by L5 and L6 spinal nerve ligation in male Sprague-Dawley rats. The effects of intraperitoneally administered NTSR1 agonist PD 149163 was assessed using von Frey filaments. To examine the role of 5-HT neurotransmission, a serotonin (5-HT) receptor antagonist dihydroergocristine was pretreated intrathecally, and spinal microdialysis studies were performed to measure the change in extracellular level of 5-HT in response to PD 149163 administration. To investigate the supraspinal mechanism, NTSR1 antagonist 48692 was microinjected into the rostral ventromedial medulla (RVM) prior to systemic PD 149163. Additionally, the effect of intrathecal DHE on intra-RVM PD 149163 was assessed. Results: Intraperitoneally administered PD 149163 exhibited a dose-dependent attenuation of mechanical allodynia. This effect was partially reversed by intrathecal pretreatment with dihydroergocristine and was accompanied by an increased extracellular level of 5-HT in the spinal cord. The PD 149163-produced antinociception was also blocked by intra-RVM SB 48692. Direct injection of PD 149163 into the RVM mimicked the maximum effect of the same drug delivered intraperitoneally, which was reversed by intrathecal dihydroergocristine. Conclusions: These observations indicate that systemically administered NTSR1 agonist produces antinociception through the NTSR1 in the RVM, activating descending serotonergic projection to release 5-HT into the spinal dorsal horn.

• BMB Reports
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• 제54권5호
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• pp.266-271
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• 2021

Estrogen-related receptor γ (ERRγ), a member of the orphan nuclear receptor family, is a key mediator in cellular metabolic processes and energy homeostasis. Therefore, ERRγ has become an attractive target for treating diverse metabolic disorders. We recently reported that ERRγ acts as a negative regulator of osteoclastogenesis induced by receptor activator of nuclear factor-κB ligand (RANKL). In the present study, we explored the effects of an ERRγ-specific modulator, GSK5182, on ERRγ-regulated osteoclast differentiation and survival. Interestingly, GSK5182 increased ERRγ protein levels much as does GSK4716, which is an ERRγ agonist. GSK5182 inhibited osteoclast generation from bone-marrow-derived macrophages without affecting cytotoxicity. GSK5182 also attenuated RANKL-mediated expression of cFos and nuclear factor of activated T-cells cytoplasmic 1 (NFATc1), pivotal transcription factors for osteoclastogenesis. Arrested osteoclast differentiation was associated with reduced RANK expression, but not with the M-CSF receptor, c-Fms. GSK5182 strongly blocked the phosphorylation of IκBα, c-Jun N-terminal kinase, and extracellular signal-regulated kinase in response to RANKL. GSK5182 also suppressed NF-κB promoter activity in a dose-dependent manner. In addition to osteoclastogenesis, GSK5182 accelerated osteoclast apoptosis by caspase-3 activation. Together, these results suggest that GSK5182, a synthetic ERRγ modulator, may have potential in treating disorders related to bone resorption.