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葛根总黄酮对载脂蛋白E基因缺陷小鼠动脉粥样硬化斑块形成的影响 被引量:11
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作者 武迎 王绿娅 +3 位作者 张慧信 王伟 方微 肖磊 《中国动脉硬化杂志》 CAS CSCD 2006年第4期317-320,共4页
目的探讨葛根总黄酮对载脂蛋白E基因缺陷小鼠主动脉窦动脉粥样硬化斑块形成的影响。方法将载脂蛋白E基因缺陷小鼠随机分为模型组、葛根总黄酮低剂量组、葛根总黄酮高剂量组及阿托伐他汀阳性药物组。常规生物化学法测定血清总胆固醇、甘... 目的探讨葛根总黄酮对载脂蛋白E基因缺陷小鼠主动脉窦动脉粥样硬化斑块形成的影响。方法将载脂蛋白E基因缺陷小鼠随机分为模型组、葛根总黄酮低剂量组、葛根总黄酮高剂量组及阿托伐他汀阳性药物组。常规生物化学法测定血清总胆固醇、甘油三酯及高密度脂蛋白胆固醇水平;采用主动脉根部连续石蜡切片、苏木素伊红染色观察组织形态学改变,测定载脂蛋白E基因缺陷小鼠主动脉窦动脉粥样硬化斑块大小、动脉粥样硬化斑块与管腔面积比。结果4组小鼠共检出斑块65个,4组虽都有典型的粥样斑块或/及纤维斑块等中晚期动脉粥样硬化病变形成,但组织学观察发现模型组部分斑块体积较大,汇合成片,管壁弥漫性增厚,管腔较狭窄,而葛根总黄酮治疗组及阿托伐他汀阳性药物组动脉粥样硬化斑块病变较局限,管腔狭窄程度较轻,并且葛根总黄酮高、低剂量组及阿托伐他汀阳性药物组斑块面积与管腔面积之比值显著低于模型组(分别为0.11%±0.04%、0.27%±0.04%和0.76%±0.33%,P<0.01),葛根总黄酮高剂量组斑块面积与管腔面积比值显著低于葛根总黄酮低剂量组(P<0.01)。结论葛根总黄酮一定程度抑制载脂蛋白E基因缺陷小鼠动脉粥样硬化斑块进展,该作用可能与降低小鼠血脂作用无明显关系。 展开更多
关键词 病理学与病理生理学 葛根总黄酮 血清学与病理学检查 动脉粥样硬化斑块 脂蛋白e基因缺陷 小鼠
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氯沙坦对载脂蛋白E基因缺陷小鼠氧化应激及动脉粥样硬化斑块稳定性的影响 被引量:6
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作者 何继强 刘晓惠 +5 位作者 王绿娅 秦彦文 杜兰萍 方薇 王伟 武迎 《中国动脉硬化杂志》 CAS CSCD 2006年第4期325-329,共5页
目的观察血管紧张素Ⅱ1型受体拮抗剂氯沙坦对载脂蛋白E基因缺陷小鼠氧化应激及主动脉粥样斑块中血管平滑肌细胞、巨噬细胞数量影响,探讨氯沙坦稳定斑块的作用及可能机制。方法27只8周龄雄性载脂蛋白E基因缺陷小鼠随机等分三组:对照组、... 目的观察血管紧张素Ⅱ1型受体拮抗剂氯沙坦对载脂蛋白E基因缺陷小鼠氧化应激及主动脉粥样斑块中血管平滑肌细胞、巨噬细胞数量影响,探讨氯沙坦稳定斑块的作用及可能机制。方法27只8周龄雄性载脂蛋白E基因缺陷小鼠随机等分三组:对照组、氯沙坦低剂量组[5 mg/(kg.d)]及氯沙坦高剂量组[25 mg/(kg.d)],20周后处死动物。常规生物化学法测定血清一氧化氮含量、超氧化物歧化酶活性、丙二醛及血脂水平;采用HE染色法观察小鼠主动脉粥样硬化病变形成;免疫组织化学法分析粥样斑块中血管平滑肌细胞和巨噬细胞数量。结果三组间血脂水平无显著性差异;与对照组相比,氯沙坦低、高剂量组血清一氧化氮水平和超氧化物歧化酶活性均明显升高(P<0.01)、丙二醛水平显著减低(P<0.05和P<0.01),且氯沙坦低剂量和高剂量组间也有明显差异(P<0.01);氯沙坦干预后动脉粥样斑块纤维帽厚,脂质核心小;氯沙坦治疗组斑块中平滑肌细胞数量显著增加(P<0.01)、巨噬细胞数量明显降低(P<0.01),且氯沙坦高剂量组较低剂量组作用更明显(P<0.01)。结论氯沙坦在不影响血脂水平情况下,可通过减轻载脂蛋白E基因缺陷小鼠氧化应激,增加斑块中平滑肌细胞数量,降低巨噬细胞数量,可能起到稳定粥样斑块作用,且随剂量增加作用增强。 展开更多
关键词 病理学 氯沙坦影响小鼠主动脉粥样斑块稳定性 He染色 脂蛋白e基因缺陷小鼠 氧化应激 动脉粥样斑块 氯沙坦
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外膜炎症诱发载脂蛋白E基因敲除鼠冠状动脉粥样硬化病灶 被引量:2
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作者 高琳琳 翟同钧 +4 位作者 陈融 王建丽 李莉 胡维诚 P.D.Polinsky 《中国动脉硬化杂志》 CAS CSCD 2003年第5期415-418,共4页
研究载脂蛋白E基因敲除(载脂蛋白E°)小鼠冠状动脉内粥样硬化病灶的分布、组成与动脉外膜炎症的关系.取载脂蛋白E°小鼠心脏作连续切片,Movat法染色,追踪冠状动脉主干及其心肌内的小分支;寻找病灶,观察病灶内组成,分析其分布规... 研究载脂蛋白E基因敲除(载脂蛋白E°)小鼠冠状动脉内粥样硬化病灶的分布、组成与动脉外膜炎症的关系.取载脂蛋白E°小鼠心脏作连续切片,Movat法染色,追踪冠状动脉主干及其心肌内的小分支;寻找病灶,观察病灶内组成,分析其分布规律.复制小鼠股动脉外膜无菌性炎症模型,用免疫组织化学方法检查内膜粘附分子的表达.结果发现,冠状动脉主干内有延伸病灶,在主干以下分支(包括心肌内小分支)内有在原位生成的病灶,在两类病灶相邻的外膜有炎性细胞浸润,外膜炎症面积大于动脉粥样硬化病灶累及的内膜面积,亦发现一些部位血管外有炎性细胞浸润,而尚无病灶形成.原位病灶均发生于心室壁,大的原位病灶多发生在左室壁心肌内、血管分支处和乳头肌附近的冠状动脉分支内.股动脉外膜炎症可诱发内膜表达细胞间粘附分子1和血管细胞粘附分子1,同时伴白细胞的附壁.以上提示:血管外膜炎症是小鼠冠状动脉内病灶的一个始动环节. 展开更多
关键词 病理学 动脉粥样硬化 脂蛋白e基因敲除小鼠 冠状动脉 外膜炎症 细胞间粘附分子1 血管细胞粘附分子1
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脂蛋白E基因多态性与骨质疏松性髋部骨折
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作者 陶军 许永武 《江西医药》 CAS 2003年第2期151-154,共4页
骨质疏松症是一种多因素性疾病.主要特征是单位体积骨量减少,骨脆性增加.骨质疏松症的严重危害是并发骨折即骨质疏松性骨折:主要包括桡骨远端骨折、脊柱骨折及髋部骨折;其中髋部骨质疏松患者由于骨转换出现特异性改变,骨形成与骨吸收失... 骨质疏松症是一种多因素性疾病.主要特征是单位体积骨量减少,骨脆性增加.骨质疏松症的严重危害是并发骨折即骨质疏松性骨折:主要包括桡骨远端骨折、脊柱骨折及髋部骨折;其中髋部骨质疏松患者由于骨转换出现特异性改变,骨形成与骨吸收失耦合,导致股骨近端骨显微结构发生明显退变,骨组织力学性能下降,因此更易诱发骨折,髋部骨质疏松性骨折又因其致残、致死率高,后果最为严重,尤为受到重视. 展开更多
关键词 脂蛋白e基因 多态性 骨质疏松 髋部骨折
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胰岛素样生长因子1、载脂蛋白酶E基因多态性与阿尔茨海默病关系的研究 被引量:3
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作者 李芳芳 王建平 蒋超 《中风与神经疾病杂志》 北大核心 2017年第8期696-699,共4页
目的探讨河南省汉族人群胰岛素样生长因子1(insulin like growth factor 1,IGF-1)基因rs972936位点多态性、载脂蛋白酶E(Apo E)基因多态性与阿尔茨海默病(Alzheimer’s disease,AD)之间的相关性。方法选取58例AD患者和126例年龄、性别... 目的探讨河南省汉族人群胰岛素样生长因子1(insulin like growth factor 1,IGF-1)基因rs972936位点多态性、载脂蛋白酶E(Apo E)基因多态性与阿尔茨海默病(Alzheimer’s disease,AD)之间的相关性。方法选取58例AD患者和126例年龄、性别相匹配的健康对照(ND)者为研究对象,柱层析法提取外周血基因组DNA,采用PCR和基因测序技术检测IGF-1基因rs972936位点及Apo E基因型多态分布,并进行对比分析。结果与ND组比较,AD组IGF-1基因rs972936位点3种基因型分布总体差异有统计学意义(χ~2=6.108,P=0.047),其中AD组中GG基因型的频率高于对照组(70.7%>51.6%,χ~2=5.935,P=0.015),G等位基因频率明显高于健康对照组(χ~2=6.502,P=0.011);AD组Apo Eε4等位基因频率可能增加AD的患病风险(OR=2.872,95%CI 1.542~5.351)(P=0.001);Apo Eε4等位基因不影响IGF-1基因rs972936位点的基因型或等位基因的分布频率(P>0.05)。结论 IGF-1基因rs972936位点多态性与河南汉族人群AD的发病可能有相关性,其中GG基因型、G等位基因可能是AD发病的独立于Apo Eε4等位基因的危险因素。Apo Eε4等位基因是散发性AD的主要危险因素。 展开更多
关键词 胰岛素样生长因子1基因 蛋白e基因 基因多态性 阿尔茨海默病 汉族
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原肌球蛋白3在雄性ApoE基因敲除小鼠动脉粥样硬化组织中的表达 被引量:1
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作者 李程 吴思 +3 位作者 孙峥嵘 刘聪 李玲 邱阳 《中国医科大学学报》 CAS CSCD 北大核心 2021年第2期168-171,共4页
以脂蛋白E基因敲除(ApoE-/-)的雄性小鼠为研究对象,建立动脉粥样硬化模型。应用免疫组化技术检测原肌球蛋白3(TPM3)在动脉粥样硬化组织中的表达情况。HE染色结果表明ApoE-/-雄性小鼠动脉粥样硬化模型建立成功。免疫组化结果显示,与C57BL... 以脂蛋白E基因敲除(ApoE-/-)的雄性小鼠为研究对象,建立动脉粥样硬化模型。应用免疫组化技术检测原肌球蛋白3(TPM3)在动脉粥样硬化组织中的表达情况。HE染色结果表明ApoE-/-雄性小鼠动脉粥样硬化模型建立成功。免疫组化结果显示,与C57BL/6J小鼠比较,ApoE-/-雄性小鼠动脉粥样硬化组织的内皮及斑块内广泛存在TPM3表达(P<0.05)。因此认为雄性ApoE-/-小鼠动脉粥样硬化组织中TPM3表达显著升高。 展开更多
关键词 原肌球蛋白3 免疫组织化学 动脉粥样硬化 脂蛋白e基因敲除小鼠
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The Effects of Apolipoprotein E Polymorphism on Serum Lipids, Lipoproteins and Apolipoproteins Variation 被引量:3
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作者 潘闽 朱健华 +2 位作者 袁瑾 王惠民 刘志华 《Journal of Nanjing Medical University》 2003年第4期196-200,共5页
Objective: To study the effects of Apolipoprotein E (ApoE) polymorphism onserum levels of lipids, lipoproteins and apolipoproteins. Methods: Fragments of ApoE gene forthex-on containing codon 112 and 158 polymorphic l... Objective: To study the effects of Apolipoprotein E (ApoE) polymorphism onserum levels of lipids, lipoproteins and apolipoproteins. Methods: Fragments of ApoE gene forthex-on containing codon 112 and 158 polymorphic locus were amplified by PCR, and then digested untilCfo I endonuclease. Genotypes and alleles frequencies of 168 healthy persons in Jiangsu area werecalculated. The effects of ApoE genotypes and alleles on serum lipids, lipoproteins andapolipoproteins variation were analyzed. Results: The effects of ApoE alleles on total cholesterol(TC), law density lipoprotein-cholesterol (LDL-C), ApoB was: along a decreasing gradientε_4>ε_3>ε_2. The effect of ε_4 allele was to increase serum levels of TC, LDL-C and ApoB, andthe ε_2 allele had an effect opposite to that of ε_4 allele. Conclusion: ApoE polymorphism is anindependent genetic factor on individual serum levels of lipids and apolipoproteins. 展开更多
关键词 Apolipoprotein e POLYMORPHISM polymerase chain reaction restrictionfragment length polymorphism
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APOLIPOPROTEIN E GENE POLYMORPHISMS AND RISK FOR CORONARY ARTERY DISEASE IN CHINESE XINJIANGUYGUR AND HAN POPULATION 被引量:17
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作者 Sheng-liYang Bing-xianHe +5 位作者 Hui-liangLiu Zuo-yunHe HuaZhang Jian-pingLuo Xiu-fangHong Yang-chunZou 《Chinese Medical Sciences Journal》 CAS CSCD 2004年第2期150-154,共5页
Objective To examine the relationship between apolipoprotein E (Apo E) gene polymorphism and risk of coronary artery disease (CAD), analyzing association of polymorphism with classical risk factors. Methods A total of... Objective To examine the relationship between apolipoprotein E (Apo E) gene polymorphism and risk of coronary artery disease (CAD), analyzing association of polymorphism with classical risk factors. Methods A total of 124 patients (including 84 Han population and 40 Uygur population) with angiographically verified CAD or myocardial infarction were prospectively evaluated. Data referring to hypertension, diabetes, and tobacco consump-tion were recorded. The levels of total cholesterol (TC), high density lipoprotein (HDL) cholesterol, Apo A1 and B, and triglycerides (TG) were determined. DNA was obtained from 124 patients and 70 controls. In order to determine Apo E genotypes, DNA was PCR amplified and digested with HhaI. The genetic polymorphism of Apo E is due to three common alleles, epsilon(ε) 2, ε3, ε4, at a single autosomal gene locus. These alleles determine the six phenotypes E2/2, E3/3, E4/4, E4/2, E4/3, and E3/2. Results In Uygur population, the frequency of the ε2, ε3, and ε4 was 0.155, 0.648, and 0.197 respectively. In Han po-pulation, the frequency of the ε2, ε3, and ε4 was 0.081, 0.772, and 0.146 respectively. In the patient group, the frequency of the ε2, ε3, and ε4was 0.060, 0.758, and 0.182 respectively. In the control group, the frequency of the ε2, ε3, and ε4 was 0.193, 0.671, and 0.136 respectively. ε2 frequency of Uygur’ patients and controls was 0.050 and 0.290 respectively. Serum low density lipoprotein (LDL) cholesterol, TC, and TG values tended to decrease from the Apo E-4 phenotypes to Apo E-2 phenotypes. When deletion polymorphism of ε2 was compared with the common risk factors for CAD, its risk ratio (RR) is 4.38. Conclusions These studies confirm and find that Apo E phenotype distribution in Uygur population differs significantly from that in Han population in Xinjiang. CAD patients have significantly lower ε2 allele and slightly higher ε3 or ε4 allele frequency than controls, especially in Uygur population. It shows protective effects of ε2 on CAD. 展开更多
关键词 apolipoprotein e DNA polymorphisms risk factors coronary artery disease
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Study of apolipoprotein E genetic polymorphism in patients with atherosclerotic cerebral infarction 被引量:2
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作者 罗本燕 陈智 +2 位作者 陈峰 李霞 潘小平 《Journal of Zhejiang University Science》 CSCD 2003年第6期749-752,共4页
Objective: To explore the frequency and significance of ApoE gene polymorphisms in Chinese patients with atherosclerotic cerebral infarction (ACI). Methods: Polymerase chain reaction and gene sequencing, single nucleo... Objective: To explore the frequency and significance of ApoE gene polymorphisms in Chinese patients with atherosclerotic cerebral infarction (ACI). Methods: Polymerase chain reaction and gene sequencing, single nucleotide polymorphisms of ApoE gene were used to analyze 33 cases of patients with ACI and 35 controls. Results: The frequencies of ApoE gene single nucleotide polymorphisms 465C/G, 462C/G and 451delC in the ACI group were significantly higher than those in the control group (P<0.05). The prevalence of polymorphism 486G/T in the control group was significantly higher than that in the ACI group ( P = 0.011) . Conclusions: 465C/G,462C/G and 451delC polymorphisms might be associated with ACI.486GT allele might have protective effect on the pathogenesis of ACI. 展开更多
关键词 Cerebral infarction ATHeROSCLeROTIC GeNeTICS Apoe allele Single nucleotide polymorphism
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GENE POLYMORPHISM OF APOLIPOPROTEIN E AND CORTICAL CEREBRAL INFARCTION
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作者 张颖冬 梁秀龄 《Chinese Medical Sciences Journal》 CAS CSCD 1998年第4期248-251,共4页
The polymorphism of apoE, an important determinant in the lipid metabolism, may be related to the atherosclerotic events. In this study, the apoE genotypes, by means of PCR AFLP assay in ... The polymorphism of apoE, an important determinant in the lipid metabolism, may be related to the atherosclerotic events. In this study, the apoE genotypes, by means of PCR AFLP assay in 42 patients with cortical cerebral infarction and 85 healthy controls were detected. The results showed that the apoE ε 3/3 genotype was more prevalent in the controls (55.29%), and ε 3/4 genotype was more common in the patients (57.14%). The frequency of ε 4 allele was more predominate in the patients than that in the controls. The ε 3/4 genotype or ε 4 allele was associated with 2.44 or 2.31 fold increase in the risk of cortical cerebral infarction. Therefore, it was suggested that apoE ε 4 allele is a genetic factor of susceptibility to cerebral infarction, which supported the hypothesis of the association between apoE polymorphism and atherosclerotic cardio cerebrovascular disorders. 展开更多
关键词 apolipoprotein e POLYMORPHISM cerebral infarction
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APOLIPOPROTEIN E POLYMORPHISM AND ALZHERMER'S DISEASE
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作者 张曙云 葛炜 +1 位作者 程吟梅 朱建中 《Chinese Medical Sciences Journal》 CAS CSCD 1998年第2期123-125,共3页
We determined and analysed the ApoE polymorphism of 30 sporadic Alzheimer’s disease (AD) pa- tients, 27 patients with multi-infarct dementia (MID) and 46 aged healthy subjects as control. The results showed that the ... We determined and analysed the ApoE polymorphism of 30 sporadic Alzheimer’s disease (AD) pa- tients, 27 patients with multi-infarct dementia (MID) and 46 aged healthy subjects as control. The results showed that the frequency of ApoE E4/3 genetype in AD group was significantly higher than that in con- trol (P<0. 05). Among these three groups, ApoE 4 allele frequency in AD group was significantly higher than that in control (P<0. 01 ) and MID group (P<0. 05). Among the three ApoE alleles, the risk ratio of ApoE E4 allele in AD group was 4. 114(p<0. 01 ). There was statistically significant (P<0. 05) as the increasing of ApoE 4 gene dose in AD. It suggests that ApoE is related to AD of Chineses and it might be a genetics index of early diagnosis for AD. 展开更多
关键词 apolipoprotein e POLYMORPHISM Alzheimer's disease
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聪明由何而来
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作者 张唯诚 《海峡科技》 2003年第8期33-33,共1页
关键词 心理学 智力测验 G要素 智慧基因 基因变体 阿朴脂蛋白e基因 智商
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Apolipoprotein E polymorphism in the early onset of coronary heart disease
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作者 杨志健 朱铁兵 +5 位作者 马根山 尹航 钱卫冲 张馥敏 曹克将 马文珠 《Chinese Medical Journal》 SCIE CAS CSCD 2001年第9期87-89,110,共4页
Objective To assess the relationship between apolipoprotein E (apoE) polymorphism and the early onset of coronary heart disease (CHD) and the effect of apoE on lipids and lipoproteins in healthy Chinese subjects. Met... Objective To assess the relationship between apolipoprotein E (apoE) polymorphism and the early onset of coronary heart disease (CHD) and the effect of apoE on lipids and lipoproteins in healthy Chinese subjects. Methods Sixty-eight patients with CHD younger than 55 years (CHD1), 136 patients with CHD older than 65 years (CHD2), and 136 healthy subjects were enrolled, and their plasma levels of triglyceride (TG), total cholesterol (TC) and high density lipoprotein cholesterol (HDL-C) were determined. The apoE genotypes were identified by polymerase chain reaction-restriction fragment length polymorphism. Results apoE 3/4 genotype and E4 allele frequency in the CHD1 group were higher than those in the CHD2 group and healthy subjects, while no differences were found between CHD2 and healthy subjects. Meanwhile, the plasma levels of TC and low density lipoprotein cholesterol (LDL-C) were higher in the CHD2 group than in both CHD1 group and healthy subjects.Each apoE isoprotein has variable TC and LDL-C levels that is E2 (E2/2+E2/3)<E3(E3/3)<E4(E4/4+E3/4). Conclusion apoE is one of the genetic factors that affect TC and LDL-C levels, and apoE 4 has a very close relation to CHD, suggesting that apoE 4 is an independent genetic factor of the early onset of CHD. 展开更多
关键词 coronary heart disease · early onset · apolipoprotein e · polymorphism
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Apolipoprotein E gene polymorphism and its association with human longevity in the Uygur nationality in Xinjiang 被引量:1
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作者 王新利 王国荃 +1 位作者 杨春荣 李萱 《Chinese Medical Journal》 SCIE CAS CSCD 2001年第8期34-37,104,共5页
Objective To study the relationship between apoE alleles and life-span. Methods Apolipoprotein E genotypes were determined in 164 unrelated Uygurs including 35 persons aged 90 years or older, 71 men aged 20-35 and 5... Objective To study the relationship between apoE alleles and life-span. Methods Apolipoprotein E genotypes were determined in 164 unrelated Uygurs including 35 persons aged 90 years or older, 71 men aged 20-35 and 54 men with myocardial infarction by using polymerase chain reaction-restriction fragment length polymorphism. Apolipoprotein E gene polymorphism was analyzed among three groups. Results There was statistically significant difference in the ε4 allele frequencies among three groups. The ε4 allele frequency in olds was the lowest (0.057), while in patients suffering from myocardial infarction (MI) was the highest (0.213). In MI patients the average age of first attack in ε4 allele carriers was significantly younger than that of non-carries, 51.3 and 58.3 years, respectively (P<0.05). Conclusion ApoE genotype may have some impact on human longevity. 展开更多
关键词 apolipoprotein e · gene · longevity · Uy gur
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Genetic susceptibility to traumatic brain injury and apolipoprotein E gene 被引量:5
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作者 孙晓川 江涌 《Chinese Journal of Traumatology》 CAS 2008年第4期247-252,共6页
Traumatic brain injury (TBI) is defined as an injury caused by a blow or jolt to the head or a penetrating head injury that disrupts the normal function of the brain. It is a common emergency and severe case in neur... Traumatic brain injury (TBI) is defined as an injury caused by a blow or jolt to the head or a penetrating head injury that disrupts the normal function of the brain. It is a common emergency and severe case in neurosurgery field. Nowadays, there are more and more evidences showing that TBI, which is apparently similar in pathology and severity in the acute stage, may have different outcomes. The known prognostic factors (such as age, severity of injury and treatments, etc.) explain only part of this variability and the concept of genetic susceptibility of traumatic brain injury has already been accepted by more and more people. It is now demonstrated that genetic polymorphism may play a key role in the susceptibility to TBI, even outcome follow-ing TBI. Although there are many genes that may involved in pathophysiological processes influencing TBI, apolipoprotein E gene has become one of the most extensive studied genes in neurotrauma and neurodegenerative disease and seems to take an important part in the neural responses to TBI. In this article, we will review the current understanding of the genetic susceptibility of TBI and the advancements regarding the impact of apolipoprotein E genotype on the severity and/or outcome following TBI. 展开更多
关键词 Brain injuries Genetic predisposition to disease GeNeS
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