• 제목/요약/키워드: brc-2

검색결과 26건 처리시간 0.021초

결합재와 혼화재 종류에 따른 콘크리트의 수화반응 특성 (Hydration Reaction Properties of Concrete With Binders and Admixtures)

  • 조일호;성찬용
    • 한국농공학회논문집
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    • 제50권2호
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    • pp.27-34
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    • 2008
  • Recently, owing to the development of industry and improvement of building techniques, concrete structures are becoming larger and higher. This study was performed to analyze hydration reation properties of concrete with binders and admixtures, such as OPC, low heat cement, belite rich cement, slag powder, lime powder and fly ash. To investigate effects of PC type superplasticizer on the hydration, experiments involving FT-IR, XRD, DSC, SEM were analyzed at the curing age 1day, 3days and 28days. The hydration reaction rate of OPC concrete slightly delayed at the curing age 1day, blast furnace slag powder and fly ash were more effective. BRC and LHC concretes can be used for concrete structures in winter season.

MAGNETIC FIELDS IN BRIGHT-RIMMED CLOUDS AND COMETARY GLOBULES TRACED USING R-BAND POLARIZATION OBSERVATIONS

  • SOAM, ARCHANA;GOPINATHAN, MAHESWAR;LEE, CHANG WON;BHATT, HRISH
    • 천문학논총
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    • 제30권2호
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    • pp.87-88
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    • 2015
  • We present results of our R-band polarimetry of a bright-rimmed cloud, IC1396A (with BRC 36), associated with the H II region S131 and the cometary globule LDN 1616 to study their magnetic field geometry. The distances of these clouds have been reported to be ~ 750 pc and ~ 450 pc, respectively in the literature. The young open cluster Trumpler 37 in the vicinity of IC1396A and the high mass stars in the Orion belt near L1616 are found to be responsible for the structure of these clouds. We made polarimetry of foreground stars inferred from their distances measured by the Hipparcos satellite to subtract the foreground contribution to the observed polarization results. We discuss the optical polarimetric results and compare our findings with MHD simulations towards BRCs and CGs.

Inhibitory effects of total saponin from Korean Red Ginseng on [Ca2+]i mobilization through phosphorylation of cyclic adenosine monophosphate-dependent protein kinase catalytic subunit and inositol 1,4,5-trisphosphate receptor type I in human platelets

  • Shin, Jung-Hae;Kwon, Hyuk-Woo;Cho, Hyun-Jeong;Rhee, Man Hee;Park, Hwa-Jin
    • Journal of Ginseng Research
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    • 제39권4호
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    • pp.354-364
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    • 2015
  • Background: Intracellular $Ca^{2+}$($[Ca^{2+}]_i$) is a platelet aggregation-inducing molecule. Therefore, understanding the inhibitory mechanism of $[Ca^{2+}]_i$mobilization is very important to evaluate the antiplatelet effect of a substance. This study was carried out to understand the $Ca^{2+}$-antagonistic effect of total saponin from Korean Red Ginseng (KRG-TS). Methods: We investigated the $Ca^{2+}$-antagonistic effect of KRG-TS on cyclic nucleotides-associated phosphorylation of inositol 1,4,5-trisphosphate receptor type I ($IP_3RI$) and cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA) in thrombin (0.05 U/mL)-stimulated human platelet aggregation. Results: The inhibition of $[Ca^{2+}]_i$ mobilization by KRG-TS was increased by a PKA inhibitor (Rp-8-BrcAMPS), which was more stronger than the inhibition by a cyclic guanosine monophosphate (cGMP)- dependent protein kinase (PKG) inhibitor (Rp-8-Br-cGMPS). In addition, Rp-8-Br-cAMPS inhibited phosphorylation of PKA catalytic subunit (PKAc) ($Thr^{197}$) by KRG-TS. The phosphorylation of $IP_3RI$ ($Ser^{1756}$) by KRG-TS was very strongly inhibited by Rp-8-Br-cAMPS compared with that by Rp-8-BrcGMPS. These results suggest that the inhibitory effect of $[Ca^{2+}]_i$ mobilization by KRG-TS is more strongly dependent on a cAMP/PKA pathway than a cGMP/PKG pathway. KRG-TS also inhibited the release of adenosine triphosphate and serotonin. In addition, only G-Rg3 of protopanaxadiol in KRG-TS inhibited thrombin-induced platelet aggregation. Conclusion: These results strongly indicate that KRG-TS is a potent beneficial compound that inhibits $[Ca^{2+}]_i$ mobilization in thrombin-platelet interactions, which may result in the prevention of platelet aggregation-mediated thrombotic disease.

결합재 조건에 따른 콘크리트의 수화발열 특성에 관한 연구 (The Experimental Study on the Heat Hydration Properties of Concrete According to Binder Conditions)

  • 최성우;조현태;유득현
    • 콘크리트학회논문집
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    • 제18권6호
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    • pp.769-776
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    • 2006
  • 최근 급속한 산업의 발달과 더불어 토목 건축기술의 발달로 콘크리트 구조물의 초고층화 대형화가 이루어 지고 있으며, 이러한 대형 구조물의 시공에 있어서 콘크리트의 온도상승은 부재의 내 외부 온도차이로 인한 온도응력에 의하여 균열을 발생시켜 구조물의 내하력 및 내구성에 심각한 손상을 가져올 수 있다. 연구에서는 시멘트 및 혼화재의 종류 및 배합설계 조건에 따라 콘크리트의 수화발열 특성 및 콘크리트의 공학적 특성에 대해 실험을 진행하였다. 시멘트 종류는 1종 보통포틀랜드시멘트, 혼합시멘트인 고로슬래그시멘트 및 4종 포틀랜드시멘트(벨라이트시멘트)를 사용하였으며, 혼화재 종류로는 플라이애쉬와 고로슬래그미분말을 사용하였다. 혼화재의 사용방법은 일반적으로 사용되는 플라이애쉬 25% 대체한 경우와 비교용으로 고로슬래그미분말을 50% 대체한 경우(2성분계 배합)와 또는 플라이애쉬와 혼합 사용(3성분계 배합) 방법을 적용하였다. 본 연구 결과, 결합재 종류 및 설계 조건에 따른 수화발열특성에 있어서는 벨라이트시멘트를 사용하는 것이 가장 효과적이며, 플라이애쉬를 사용한 경우도 수화열 저감 효과는 우수한 것으로 나타났으며, 수화발열특성을 비롯한, 콘크리트의 품질 특성을 종합적으로 고려할 경우, 고로슬래그미분말의 사용이 효과적이며, 특히 고로슬래그미분말과 플라이애쉬를 혼합사용한 3성분계의 배합설계가 가장 효과적인 것으로 판단된다.

DNA Strand Breaks in Mitotic Germ Cells of Caenorhabditis elegans Evaluated by Comet Assay

  • Park, Sojin;Choi, Seoyun;Ahn, Byungchan
    • Molecules and Cells
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    • 제39권3호
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    • pp.204-210
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    • 2016
  • DNA damage responses are important for the maintenance of genome stability and the survival of organisms. Such responses are activated in the presence of DNA damage and lead to cell cycle arrest, apoptosis, and DNA repair. In Caenorhabditis elegans, double-strand breaks induced by DNA damaging agents have been detected indirectly by antibodies against DSB recognizing proteins. In this study we used a comet assay to detect DNA strand breaks and to measure the elimination of DNA strand breaks in mitotic germline nuclei of C. elegans. We found that C. elegans brc-1 mutants were more sensitive to ionizing radiation and camptothecin than the N2 wild-type strain and repaired DNA strand breaks less efficiently than N2. This study is the first demonstration of direct measurement of DNA strand breaks in mitotic germline nuclei of C. elegans. This newly developed assay can be applied to detect DNA strand breaks in different C. elegans mutants that are sensitive to DNA damaging agents.

Involvement of Crosstalk Between cAMP and cGMP in Synaptic Plasticity in the Substantia Gelatinosa Neurons

  • Kim, Tae-Hyung;Chung, Ge-Hoon;Park, Seok-Beom;Chey, Won-Young;Jun, Sung-Jun;Kim, Joong-Soo;Oh, Seog-Bae
    • International Journal of Oral Biology
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    • 제36권2호
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    • pp.83-89
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    • 2011
  • Substantia gelatinosa (SG) neurons receive synaptic inputs from primary afferent $A{\delta}$- and C-fibers, where nociceptive information is integrated and modulated by numerous neurotransmitters or neuromodulators. A number of studies were dedicated to the molecular mechanism underlying the modulation of excitability or synaptic plasticity in SG neurons and revealed that second messengers, such as cAMP and cGMP, play an important role. Recently, cAMP and cGMP were shown to downregulate each other in heart muscle cells. However, involvement of the crosstalk between cAMP and cGMP in neurons is yet to be addressed. Therefore, we investigated whether interaction between cAMP and cGMP modulates synaptic plasticity in SG neurons using slice patchclamp recording from rats. Synaptic activity was measured by excitatory post-synaptic currents (EPSCs) elicited by stimulation onto dorsal root entry zone. Application of 1 mM of 8-bromoadenosine 3,5-cyclic monophosphate (8-Br-cAMP) or 8-bromoguanosine 3,5-cyclic monophosphate (8-Br-cGMP) for 15 minutes increased EPSCs, which were maintained for 30 minutes. However, simultaneous application of 8-BrcAMP and 8-Br-cGMP failed to increase EPSCs, which suggested antagonistic cross-talk between two second messengers. Application of 3-isobutyl-1-methylxanthine (IBMX) that prevents degradation of cAMP and cGMP by blocking phosphodiesterase (PDE) increased EPSCs. Co-application of cAMP/cGMP along with IBMX induced additional increase in EPSCs. These results suggest that second messengers, cAMP and cGMP, might contribute to development of chronic pain through the mutual regulation of the signal transduction.