四川西部地区地理环境复杂,滑坡空间结构多样且变形剧烈。为有效预防滑坡灾害,需要探究相关区域滑坡危险性可靠评价方法。利用G1-熵权耦合赋权逼近理想解排序法(technique for order preference by similarity to ideal solution,TOPSIS...四川西部地区地理环境复杂,滑坡空间结构多样且变形剧烈。为有效预防滑坡灾害,需要探究相关区域滑坡危险性可靠评价方法。利用G1-熵权耦合赋权逼近理想解排序法(technique for order preference by similarity to ideal solution,TOPSIS)构建滑坡灾害危险性评价模型,选取高程、降雨、地震动参数等12个评价因子,对雅砻江滑坡灾害危险性进行评价。依据贴近度将滑坡区域分为4个等级,即高危险区(0.75~1)、较高危险区(0.5~0.75)、中等危险区(0.25~0.5)和低危险区(0~0.25)。同时,对比了由差分干涉测量短基线集时序分析(small baseline subset interferometric synthetic aperture radar,SBAS-InSAR)技术得到的4个区域滑坡实测结果和本文评价模型的分析结果。利用G1-熵权耦合赋权TOPSIS得到九龙县烟袋镇桤木林村高生地滑坡、新龙县和平乡甲西村麻西滑坡、德格县年古乡政府滑坡和甘孜县扎科乡达玛滑坡的贴近度分别为0.854、0.686、0.405和0.224,由SBAS-InSAR技术得到滑坡前缘局部变形速率分别为-150、-43、-66、30 mm/a,二者之间有显著的对应关系,证明本文评价模型的准确性。应用G1-熵权耦合赋权TOPSIS法对滑坡危险性评价具有较高的准确性,该方法可为其他地区滑坡地质灾害评价提供参考。展开更多
Krill oil(KO)exhibits various biological activities,such as anti-inflammatory and antitumor effects.However,the inhibitory effects of benign prostatic hyperplasia(BPH)in vitro and in vivo have not yet been studied.Thi...Krill oil(KO)exhibits various biological activities,such as anti-inflammatory and antitumor effects.However,the inhibitory effects of benign prostatic hyperplasia(BPH)in vitro and in vivo have not yet been studied.This study investigated the anti-BPH effects of KO extracted by an enzymatic hydrolysis method.KO treatment inhibited the proliferation of WMPY-1 and BPH-1 cells by induction of G0/G1 phase arrest through the modulation of positive and negative regulators in both prostate cell types.KO treatment stimulated phosphorylation of c-Jun N-terminal kinase(JNK)and p38 signaling.In addition,KO changed the expression of BPH-related markers(5α-reductase,androgen receptor,FGF,Bcl-2,and Bax)and the activity of the proliferation-mediated NF-κB binding motif.KO-induced levels of proliferation-mediated molecules of prostate cells were attenuated in the presence of siRNA-specific p-38(si-p38)and JNK(si-JNK).Furthermore,the administration of KO alleviated prostate size and weight and the cell layer thickness of prostate glands in a testosterone enanthate-induced BPH rat model.KO treatment altered the level of dihydrotestosterone in serum and the expression levels of BPH-related markers in prostate tissues.Finally,KO-mediated inhibition of prostatic growth was validated by histological analysis.These results suggest that KO has an inhibitory effect on BPH in prostate cells in vitro and in vivo.Thus,KO might be a potential prophylactic or therapeutic agent for patients with BPH.展开更多
文摘四川西部地区地理环境复杂,滑坡空间结构多样且变形剧烈。为有效预防滑坡灾害,需要探究相关区域滑坡危险性可靠评价方法。利用G1-熵权耦合赋权逼近理想解排序法(technique for order preference by similarity to ideal solution,TOPSIS)构建滑坡灾害危险性评价模型,选取高程、降雨、地震动参数等12个评价因子,对雅砻江滑坡灾害危险性进行评价。依据贴近度将滑坡区域分为4个等级,即高危险区(0.75~1)、较高危险区(0.5~0.75)、中等危险区(0.25~0.5)和低危险区(0~0.25)。同时,对比了由差分干涉测量短基线集时序分析(small baseline subset interferometric synthetic aperture radar,SBAS-InSAR)技术得到的4个区域滑坡实测结果和本文评价模型的分析结果。利用G1-熵权耦合赋权TOPSIS得到九龙县烟袋镇桤木林村高生地滑坡、新龙县和平乡甲西村麻西滑坡、德格县年古乡政府滑坡和甘孜县扎科乡达玛滑坡的贴近度分别为0.854、0.686、0.405和0.224,由SBAS-InSAR技术得到滑坡前缘局部变形速率分别为-150、-43、-66、30 mm/a,二者之间有显著的对应关系,证明本文评价模型的准确性。应用G1-熵权耦合赋权TOPSIS法对滑坡危险性评价具有较高的准确性,该方法可为其他地区滑坡地质灾害评价提供参考。
基金supported by the Basic Science Research Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Education(2018R1A6A1A03025159).
文摘Krill oil(KO)exhibits various biological activities,such as anti-inflammatory and antitumor effects.However,the inhibitory effects of benign prostatic hyperplasia(BPH)in vitro and in vivo have not yet been studied.This study investigated the anti-BPH effects of KO extracted by an enzymatic hydrolysis method.KO treatment inhibited the proliferation of WMPY-1 and BPH-1 cells by induction of G0/G1 phase arrest through the modulation of positive and negative regulators in both prostate cell types.KO treatment stimulated phosphorylation of c-Jun N-terminal kinase(JNK)and p38 signaling.In addition,KO changed the expression of BPH-related markers(5α-reductase,androgen receptor,FGF,Bcl-2,and Bax)and the activity of the proliferation-mediated NF-κB binding motif.KO-induced levels of proliferation-mediated molecules of prostate cells were attenuated in the presence of siRNA-specific p-38(si-p38)and JNK(si-JNK).Furthermore,the administration of KO alleviated prostate size and weight and the cell layer thickness of prostate glands in a testosterone enanthate-induced BPH rat model.KO treatment altered the level of dihydrotestosterone in serum and the expression levels of BPH-related markers in prostate tissues.Finally,KO-mediated inhibition of prostatic growth was validated by histological analysis.These results suggest that KO has an inhibitory effect on BPH in prostate cells in vitro and in vivo.Thus,KO might be a potential prophylactic or therapeutic agent for patients with BPH.
