• 대한공간정보학회지
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• 제7권1호
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• pp.87-95
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• 1999

본 연구에서는 고 해상력의 IRS-1C PAN 데이터와 다중 관측파장대를 갖고 있는 Landsat TM 데이터를 PCA(principal component analysis) 기법으로 중합하고, 중합화상을 이용하여 토지이용분류를 수행, TM 원화상과 분류정확도를 비교 분석하고자 하였다. 분류결과를 평가하기 위해서 10개의 분류항목으로 구성된 sample data를 생성시켰으며, 생성된 sample data의 전체정확도(overall accuracy)로서 분류결과를 평가하였다. 그 결과 여러 밴드를 사용할 수 있다는 이점을 가진 PCA기법으로 Landsat TM 데이터와 IRS-1C PAN 데이터를 중합하여 토지이용분류를 수행할 경우, IRS-1C PAN데이터와 TM13457의 중합화상에서 95.1%로 분류정확도가 가장 높았으며, 특히 TM123457 또는 TM 13457의 중합화상의 경우 TM원화상보다 분류정확도가 가장 크게 향상(6.2%)되었다. 또한 토지이용분류에 있어서 중합칼라합성화상이 TM 원화상 보다 전체적으로 약 5.16%의 정확도 향상을 가져왔다.

• 한국측량학회지
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• 제16권2호
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• pp.187-194
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• 1998

본 연구에서는 높은 해상력의 IRS-1C PAN 데이터와 다양한 관측파장대를 갖고 있는 Landsat TM 데이터를 사용하여, 화상중합방법의 대표적 방법인 IHS방법으로 중합화상을 작성하고, IHS중합화상 및 원화상을 이용하여 토지이용분류를 수행하는데 있어서 어떤 칼라합성밴드가 유효한지를 밝히는데 그 목적이 있다. 분류결과를 평가하기 위해서 10개의 분류항목으로 구성된 sample data를 생성시켰으며, 생성된 sample data의 전체정확도(overall accuracy)로서 분류결과를 평가하였다. 그 결과 Landsat TM 데이터와 IRS-1C PAN데이터를 IHS방법으로 중합하여 토지이용분류를 수행할 경우, TM4, TM5 및 TM7의 적외선영역(infrared spectral region)의 밴드 중 2개 밴드를 포함시켜 분류를 수행하는 것이 좋았으며, 특히 TM 247 중합화상의 경우 분류정확도가 11.8%로 향상되어 가장 좋은 결과를 나타내었다. 또한 토지이용분류를 수행할 경우 3밴드를 중합하여 사용하는 경우보다 1% 원화상에 IRS-1C PAN화상을 추가하여 사용하는 경우의 정확도가 전체적으로 높았다.

• 한국측량학회지
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• 제19권4호
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• pp.373-383
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• 2001

본 연구에서는 중해상도 위성영상으로 대표적인 SPOT, 아리랑, IRS-1C위성영상에 대하여 각기 하나의 입체모델을 이용한 지도제작 실험을 수행하였으며, 각각에 대한 위치정확도, 판독 및 묘사가능한 지형지물의 분석, 기존 수치지도와의 비교 등을 통하여, 제작가능한 지도축척의 범위에 대한 기술적인 검토 및 경제성 검토를 하였다. 도화작업에 있어서, SPOT 영상은 수치입체도화기를 사용한 3차원 도화를 하였으며, 아리랑 및 IRS-lC 위성영상은 데이터에 대한 시스템 지원상의 문제가 있어서 영상정합 방법으로 수치표고모형을 생성한 후 정사보정영상을 제작하여 head-up digitizing에 의한 2차원 도화를 실시하였다. 실험 결과 중해상도 영상으로 큰 도로, 하천, 수애선 등 일부 항목에 대하여 판독과 묘사가 가능하였지만, 불가능한 항목이 많았다. 지도제작 측면에서 SPOT은 1/50,000지형도 수정용, 아리랑 및 IRS-lC는 1/25,000지형도의 수정용으로 활용이 가능하다고 판단되었다.

• Journal of Yeungnam Medical Science
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• 제36권1호
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• pp.26-35
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• 2019

Background: Dysregulation of hepatic glucose production (HGP) contributes to the development of type 2 diabetes mellitus. Telmisartan, an angiotensin II type 1 receptor blocker (ARB), has various ancillary effects in addition to common blood pressure-lowering effects. The effects and mechanism of telmisartan on HGP have not been fully elucidated and, therefore, we investigated these phenomena in hyperglycemic HepG2 cells and high-fat diet (HFD)-fed mice. Methods: Glucose production and glucose uptake were measured in HepG2 cells. Expression levels of phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase ${\alpha}$ ($G6Pase-{\alpha}$), and phosphorylation levels of insulin receptor substrate-1 (IRS-1) and protein kinase C ${\zeta}$ ($PKC{\zeta}$) were assessed by western blot analysis. Animal studies were performed using HFD-fed mice. Results: Telmisartan dose-dependently increased HGP, and PEPCK expression was minimally increased at a $40{\mu}M$ concentration without a change in $G6Pase-{\alpha}$ expression. In contrast, telmisartan increased phosphorylation of IRS-1 at Ser302 ($p-IRS-1-Ser^{302}$) and decreased $p-IRS-1-Tyr^{632}$ dose-dependently. Telmisartan dose-dependently increased $p-PKC{\zeta}-Thr^{410}$ which is known to reduce insulin action by inducing IRS-1 serine phosphorylation. Ectopic expression of dominant-negative $PKC{\zeta}$ significantly attenuated telmisartan-induced HGP and $p-IRS-1-Ser^{302}$ and -inhibited $p-IRS-1-Tyr^{632}$. Among ARBs, including losartan and fimasartan, only telmisartan changed IRS-1 phosphorylation and pretreatment with GW9662, a specific and irreversible peroxisome proliferator-activated receptor ${\gamma}$ ($PPAR{\gamma}$) antagonist, did not alter this effect. Finally, in the livers from HFD-fed mice, telmisartan increased $p-IRS-1-Ser^{302}$ and decreased $p-IRS-1-Tyr^{632}$, which was accompanied by an increase in $p-PKC{\zeta}-Thr^{410}$. Conclusion: These results suggest that telmisartan increases HGP by inducing $p-PKC{\zeta}-Thr^{410}$ that increases $p-IRS-1-Ser^{302}$ and decreases $p-IRS-1-Tyr^{632}$ in a $PPAR{\gamma}$-independent manner

• 약학회지
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• 제52권3호
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• pp.182-187
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• 2008

Salicylate (SA) was shown to alleviate insulin resistance. Here, we showed that SA inhibited Ser731 phosphorylation of insulin receptor substrate 1 (IRS1) and S6 kinase activation, and enhanced tyrosine phosphorylation of IRS1 in response to insulin or amino acid. Experiments using a cJun N-terminal kinase (JNK)-deficient cell and an IRS1 JNK-binding mutant showed that JNK is not required for Ser731 phosphorylation. A two-week treatment of obese mice with SA resulted in decreased Ser731 phosphorylation and enhanced insulin signaling. These results suggest that SA enhances insulin signaling by inhibiting Ser731 phosphorylation of IRS1.

• 한국측량학회지
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• 제17권3호
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• pp.293-300
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• 1999

IRS-1C PAN의 수치화상데이터를 사용하여 수치표고모델을 생성하는 기법을 연구하였다. 번들조정기법을 적용하여 라인별 외부표정요소를 결정하였으며, 그 결과 위성의 자세와 위치 모두에 있어서 1차다항식이 가장 유효하였다. 수치표고모델과 정사투영화상을 생성한 후, 연구 대상영역내의 상이한 표고를 가지고 있는 16점의 평가점을 선정하여, 연구결과의 지도좌표와 비교해본 결과, 표고오차의 RMSE가 $\pm{16.66m}$인 수치표고 모델을 생성할 수 있었다.

• Molecules and Cells
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• 제38권4호
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• pp.356-361
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• 2015

Mitochondrial dysfunction is associated with insulin resistance and diabetes. We previously showed that retinoid X receptor ${\alpha}$ ($RXR{\alpha}$) played an important role in transcriptional regulation of oxidative phosphorylation (OXPHOS) genes in cells with mitochondrial dysfunction caused by mitochondrial DNA mutation. In this study, we investigated whether mitochondrial dysfunction induced by incubation with OXPHOS inhibitors affects insulin receptor substrate 1 (IRS1) mRNA and protein levels and whether $RXR{\alpha}$ activation or overexpression can restore IRS1 expression. Both IRS1 and $RXR{\alpha}$ protein levels were significantly reduced when C2C12 myotubes were treated with the OXPHOS complex inhibitors, rotenone and antimycin A. The addition of $RXR{\alpha}$ agonists, 9-cis retinoic acid (9cRA) and LG1506, increased IRS1 transcription and protein levels and restored mitochondrial function, which ultimately improved insulin signaling. $RXR{\alpha}$ overexpression also increased IRS1 transcription and mitochondrial function. Because $RXR{\alpha}$ overexpression, knock-down, or activation by LG1506 regulated IRS1 transcription mostly independently of mitochondrial function, it is likely that $RXR{\alpha}$ directly regulates IRS1 transcription. Consistent with the hypothesis, we showed that $RXR{\alpha}$ bound to the IRS1 promoter as a heterodimer with peroxisome proliferator-activated receptor ${\delta}$ ($PPAR{\delta}$). These results suggest that $RXR{\alpha}$ overexpression or activation alleviates insulin resistance by increasing IRS1 expression.

• 천문학회보
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• 제43권2호
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• pp.39.1-39.1
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• 2018

We present our observational attempts to precisely measure the central mass of a proto-brown dwarf candidate, L328-IRS, in order to investigate whether L328-IRS is in the substellar mass regime. Observations were made for the central region of L328-IRS with the dust continuum and CO isotopologue line emission at ALMA band 6, discovering the detailed outflow activities and a deconvolved disk structure of a size of ${\sim}87AU{\times}{\sim}37AU$. We investigated the rotational velocities as a function of the disk radius, finding that its motions between 130 AU and 60 AU are partially fitted with a Keplerian orbit by a stellar object of ${\sim}0.30M_{\odot}$, while the motions within 60 AU do not follow any Keplerian orbit at all. This makes it difficult to lead a reliable estimation of the mass of L328-IRS. Nonetheless, our ALMA observations were useful enough to well constrain the inclination angle of the outflow cavity of L328-IRS as ${\sim}66^{\circ}$ degree, enabling us to better determine the mass accretion rate of ${\sim}8.9{\times}10^{-7}M_{\odot}yr-1$.From assumptions that the internal luminosity of L328-IRS is mostly due to this mass accretion process in the disk, or that L328-IRS has mostly accumulated the mass through this constant accretion rate during its outflow activity, its mass was estimated to be ${\sim}0.012-0.023M_{\odot}$, suggesting L328-IRS to be a substellar object. However, we leave our identification of L328-IRS as a proto-brown dwarf to be tentative because of various uncertainties especially regarding the mass accretion rate.

• 천문학회보
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• 제39권1호
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• pp.63.2-63.2
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• 2014

As a part of the "Dust, Ice, and Gas In Time" (DIGIT) key program on Herschel, we observed GSS30-IRS1, a Class I protostar located in Ophiuchus (d =125 pc), with Herschel/Photodetector Array Camera and Spectrometer (PACS). More than 70 lines were detected within a wavelength range from 50 ${\mu}m$ to 200 ${\mu}m$: CO lines from J = 14-13 to 41-40, several $H_2O$ lines of Eup = 100 K to 1500 K, 16 transitions of OH rotational lines, and two atomic [O I] lines at 63 and 145 ${\mu}m$. The [C II] line, known as a tracer of externally heated gas by the interstellar radiation field, is also detected at 158 ${\mu}m$. All lines, except [O I] and [C II], are detected only at the central spaxel of $9^{\prime\prime}.4{\times}9^{\prime\prime}.4$. The [O I] emission is extended along a NE-SW orientation, which is consistent with the known outflow direction, while the [C II] line is detected over all spaxels. One possible explanation of the detection of the [C II] line and no correlation of its spatial distribution with any other molecular emission is the existence of the enhanced ISRF nearby GSS30-IRS1. One interesting feature of GSS30-IRS1 is that the continuum emission is extended beyond the point-spread function (PSF), unlike the molecular line emission, indicative of significant external heating. The best-fit continuum model of GSS30-IRS1 with the physical structure including flared disk, envelope, and outflow shows that the internal luminosity is 11 $L_{\odot}$, and the region is also externally heated by a radiation field enhanced by a factor of 25 compared to the local standard interstellar field.

• 대한수의학회지
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• 제49권2호
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• pp.105-111
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• 2009

In this study, occurrence of canine brucellosis was surveyed in kennels, indoor dogs and stray dogs in Korea, and infrequent restriction site-polymerase chain reaction (IRS-PCR) was applied to analyze DNA polymorphism of Brucella canis (B. canis) isolates. Among a total of 501 dogs tested, B. canis antibodies by both rapid screening agglutination with 2-mercaptoethanol (2-ME RSAT) and immunochromatographic assay were detected in only 14.1% of kennel dogs. There were no seropositive cases in indoor dogs and stray dogs. DNA polymorphism was observed in 16 B. canis isolates by the IRS-PCR. Sixteen isolates were tested with primers, PsalA, PsalC, PsalG and PsalT, and different primers produced different DNA patterns. In regard to the IRS-PCR pattern of 16 isolates, 9 (56.3%) belonged to the IRS-PCR type I. The remaining 7 were differentiated as type II, III and IV. An application of the primer PsalC provided discrimination between B. canis isolated in 2005 and others.