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氨溴索对头孢哌酮/舒巴坦肺转运作用的临床研究 被引量:34
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作者 马利军 吴纪珍 +1 位作者 牛红丽 牛坡 《中国新药杂志》 CAS CSCD 北大核心 2003年第1期61-63,共3页
目的 :研究氨溴索 (沐舒坦 )临床疗效及对头孢哌酮 /舒巴坦 (舒普深 )肺转运的作用。方法 :对 1 0 6例老年肺炎患者进行随机开放平行对照试验。分为治疗组 54例 ,采用生理氯化钠溶液 1 0 0mL加头孢哌酮 /舒巴坦3 .0 g ,以 30mg·min... 目的 :研究氨溴索 (沐舒坦 )临床疗效及对头孢哌酮 /舒巴坦 (舒普深 )肺转运的作用。方法 :对 1 0 6例老年肺炎患者进行随机开放平行对照试验。分为治疗组 54例 ,采用生理氯化钠溶液 1 0 0mL加头孢哌酮 /舒巴坦3 .0 g ,以 30mg·min- 1 静滴 ,bid ,在滴注 50mL时 ,静注氨溴索 45mg ,时间不少于 5min ,bid ;对照组除不用氨溴索外 ,其他同治疗组。结果 :治疗组、对照组总有效率分别为 87.0 4 %和 78.80 % (P <0 .0 5) ,痊愈率分别为 70 .37%和57.2 4 % (P <0 .0 1 ) ;细菌清除率分别为 78.1 7%和 68.1 8% (P <0 .0 5)。痰药浓度治疗组高于对照组 (P <0 .0 1 ) ,血药浓度 2组间无显著性差异。结论 :氨溴索不仅有祛痰作用外 ,还增加头孢哌酮 /舒巴坦向肺内转运 。 展开更多
关键词 老年性肺炎 氨溴索 头孢哌酮/舒巴 转运作用
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SSAO酶抑制剂对脂肪细胞内GLUT4转运作用的研究
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作者 邓玉林 郭晓虹 +1 位作者 李明刚 张丽丽 《生命科学仪器》 2004年第1期36-39,15,共5页
SSAO酶在脂肪细胞中的含量较多,位于细胞膜上的SSAO酶的活性和其蛋白质的免疫反应性都是最大的。对于体内葡萄糖的运输和葡萄糖转运蛋白的转运,此酶起到了一定的促进作用,当它与底物在膜上反应后会引起信号传导刺激细胞内葡萄糖转运蛋白... SSAO酶在脂肪细胞中的含量较多,位于细胞膜上的SSAO酶的活性和其蛋白质的免疫反应性都是最大的。对于体内葡萄糖的运输和葡萄糖转运蛋白的转运,此酶起到了一定的促进作用,当它与底物在膜上反应后会引起信号传导刺激细胞内葡萄糖转运蛋白(GLUT4)从内部囊泡转移到细胞表面程,从而促进葡萄糖的运输和细胞对葡萄糖的吸收。如果有SSAO酶抑制剂存在,如氨基脲,二溴乙胺等,这种对GLUT4转运的促进作用就会被削弱。本研究的目的在于建立一种新的定量方法—竞争ELISA法来测试脂肪细胞膜上GLUT4的含量,从而确定SSAO酶抑制剂对GLUT4转运的作用。实验结果说明当SSAO醇抑制剂和脂肪细胞预温育一段时间后,质膜上GLUT4的含量发生下降,钒盐使得这种下降的程度加大,证明GLUT4由细胞内囊泡向细胞质膜转运的易位过程受到了抑制。此种竞争性ELISA的测试方法优点在于只需要少量的细胞膜样品就可以确定GLUT4的含量,灵敏度较高。 展开更多
关键词 SSAO酶 转运作用 脂肪细胞 葡萄糖 蛋白质 免疫反应性
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三磷酸腺苷结合盒转运体A1在泡沫细胞胆固醇流出中的作用 被引量:25
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作者 唐朝克 易光辉 +8 位作者 唐国华 王佐 王燕 刘录山 袁中华 万载阳 严鹏科 阮长耿 杨永宗 《中国动脉硬化杂志》 CAS CSCD 2003年第4期304-308,共5页
以THP 1细胞源泡沫细胞为研究对象 ,观察三磷酸腺苷结合盒转运体A1在单核—巨噬细胞源泡沫细胞胆固醇流出中的作用。实验采用流式细胞术检测的方法 ,来判断三磷酸腺苷结合盒转运体A1激动剂 2 2 (R) 羟基胆固醇和抑制剂 4 ,4 -二异硫氰... 以THP 1细胞源泡沫细胞为研究对象 ,观察三磷酸腺苷结合盒转运体A1在单核—巨噬细胞源泡沫细胞胆固醇流出中的作用。实验采用流式细胞术检测的方法 ,来判断三磷酸腺苷结合盒转运体A1激动剂 2 2 (R) 羟基胆固醇和抑制剂 4 ,4 -二异硫氰酸二丙乙烯 2 ,2 -二磺酸 (4 ,4’ diisothiocyanostilbene 2 ,2’ disulfonicacid ,DIDS)对THP 1细胞源泡沫细胞三磷酸腺苷结合盒转运体A1表达的影响。实验结果发现 ,2 2 (R) 羟基胆固醇作用THP 1细胞源泡沫细胞不同时间后 ,能明显增加细胞三磷酸腺苷结合盒转运体A1的蛋白表达 ,流式细胞术检测三磷酸腺苷结合盒转运体A1表达的平均荧光强度从 0h的 31 .1增加到 2 4h的 4 5 .2 ;而DIDS作用THP 1细胞源泡沫细胞不同时间后 ,能明显降低细胞三磷酸腺苷结合盒转运体A1的蛋白表达 ,平均荧光强度从 0h的 2 9.4降低到 2 4h的1 0 .4。胆固醇流出实验发现 ,2 2 (R) 羟基胆固醇作用THP 1细胞源泡沫细胞不同时间后 ,能明显增加细胞胆固醇流出 ;而DIDS作用THP 1细胞源泡沫细胞不同时间后 ,能明显降低细胞胆固醇流出。这些结果表明 ,三磷酸腺苷结合盒转运体A1在THP 展开更多
关键词 病理生理学 三磷酸腺苷结合盒转运体A1的作用 流式细胞术 胆固醇流出 低密度脂蛋白 泡沫细胞 22(R)-差劲基胆固醇
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囊性纤维化跨膜转运调节体氯离子通道——跨上皮离子转运的多功能引擎(英文) 被引量:11
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作者 李红宇 蔡志伟 +3 位作者 陈正豪 鞠敏 徐喆 David N.Sheppard 《生理学报》 CAS CSCD 北大核心 2007年第4期416-430,共15页
囊性纤维化跨膜转运调节体(cystic fibrosis transmembrane conductance regulator,CFTR)是ATP结合转运体超家族(ATP- binding cassette transporter superfamily)的一名特殊成员,因为它是一个具有相当复杂调控机制的氯离子通道。CFTR... 囊性纤维化跨膜转运调节体(cystic fibrosis transmembrane conductance regulator,CFTR)是ATP结合转运体超家族(ATP- binding cassette transporter superfamily)的一名特殊成员,因为它是一个具有相当复杂调控机制的氯离子通道。CFTR由五个结构域(domain)组成:两个跨膜结构域(membrane-spanning domains,MSDs),两个核苷酸结合域(nucleotide-binding domains,NBDs)和一个特殊的调控域(regulatory domain,RD)。MSDs构成一个低电导(6~12 pS)的阴离子选择性孔道(pore),其形状如同不对称的沙漏,胞外小胞内大,狭窄部分为离子筛。两个NBDs组成头尾相对的二聚体,在二聚体之间的接触面上有两个能和ATP结合的位点(位点1和位点2)。CFTR的门控机制是:ATP分子与位点1和2相互作用促使NBD二聚体的结合与解离,从而引起MSDs的构象发生变化进而使通道孔打开和关闭。RD具有多样化的结构,它含有多个磷酸化共有位点(consensus phosphorylation sites)。RD的磷酸化促进NBDs与ATP的结合,从而使CFTR得以激活。CFTR通过支架蛋白与其它膜受体以及蛋白激酶、磷酸酶形成大分子信号复合体。在复杂的细胞信号系统参与下,CFTR的功能活动在时间和空间上得到精确的调控。此外,CFTR的活动与细胞代谢有紧密联系:CFTR与代谢酶形成大分子复合体,当细胞能量需求增加时,CFTR活动会受到抑制而使细胞能量得以保存。CFTR广泛分布于机体上皮组织,它通过促进水盐转运而控制上皮细胞分泌物的量与组成。值得注意的足,在呼吸道,CFTR还对机体的防御机制起重要作用。CFTR功能失常严重影响跨上皮离子转运,进而引起或加重某些疾病。 展开更多
关键词 ATP结合转运体超家族 囊性纤维化跨膜转运调节体 囊性纤维化跨膜转运调节体相互作用蛋白 囊性纤维 化跨膜转运调节体相关疾病 囊性纤维化病 氯离子通道 跨上皮离子转运 大分子信号复合体 分泌性腹泻
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谈植物对蔗糖的利用 被引量:2
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作者 李江肃 《生物学教学》 2012年第5期62-64,共3页
本文从植物能否吸收蔗糖和植物如何利用蔗糖两方面,探讨了植物对蔗糖的利用。
关键词 质壁分离 组织培养 蔗糖 转运作用
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Overexpression of Proline Transporter Gene Isolated from Halophyte Confers Salt Tolerance in Arabidopsis 被引量:16
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作者 沈义国 张万科 +3 位作者 阎冬青 杜保兴 张劲松 陈受宜 《Acta Botanica Sinica》 CSCD 2002年第8期956-962,共7页
Proline is one of the most important and widespread osmolyte which functions in adaptation to adverse environmental stresses in many organisms. Also it is an important carbon and nitrogen resource in higher plants. Me... Proline is one of the most important and widespread osmolyte which functions in adaptation to adverse environmental stresses in many organisms. Also it is an important carbon and nitrogen resource in higher plants. Metabolism of proline has been elucidated in many plant species. However, transport of proline was poorly characterized although transport system plays an important role in proline distribution in different tissues. We isolated one full_length cDNA encoding proline transporter from the typical halophyte: Atriplex hortensis L. through cDNA library screening and 5′_RACE. The deduced amino acid sequence had eleven transmembrane domains, showed 60%-69% similarities to other ProTs and the gene was designated AhProT1. In the phylogenetic tree, higher plants' ProTs, e.g. AhProT1, showed more similar to ProP from microorganisms than ProT from mammalians. AhProT1 gene was transformed into Arabidopsis thaliana under 35S promoter. In MS medium containing [U_ 14 C] proline, AhProT1 + plants were able to accumulate much more radiolabeled proline in the roots than control plants. In MS medium containing different concentrations of NaCl, AhProT1 + plants could endure 200 mmol/L NaCl and keep development and biomass increase with proline supply, whereas control plants died back at 150 mmol/L NaCl. 展开更多
关键词 Atriplex hortensis proline transporter deposition salt stress
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降脂中药复方的转运性相互作用——体外MDR1转运研究 被引量:3
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作者 李燕娜 郭峰 +5 位作者 代卉 毛玉昌 沈智杰 侴桂新 王肖龙 胡卓汉 《现代生物医学进展》 CAS 2014年第10期1813-1817,1824,共6页
目的:药物相互作用是影响药物安全和药效的重大因素之一。本文旨在通过体外MDR1研究方法——ATP酶法,评价降脂中药复方(Fang-2)及其单方6个饮片水提物与P-gp的相互作用,为临床中西药转运性相互作用提供参考。方法:应用标准化制备技术,... 目的:药物相互作用是影响药物安全和药效的重大因素之一。本文旨在通过体外MDR1研究方法——ATP酶法,评价降脂中药复方(Fang-2)及其单方6个饮片水提物与P-gp的相互作用,为临床中西药转运性相互作用提供参考。方法:应用标准化制备技术,制备降脂中药复方及其6个饮片水提物。利用基于MDR1膜的ATP酶法,计算MDR1细胞膜的ATP酶活性,考察药物与P-gp的相互作用。结果:1 mg·mL-1、10 mg·mL-1两个浓度中药复方的ATP酶活性分别为27.2、40.0 nmol Pi·min-1·mg-1protein,呈浓度依赖性。6个单方中,泽泻、厚朴、夏枯草与P-gp作用显著,其强弱顺序为:泽泻>夏枯草>厚朴(50.6>42.6>40.0 nmol Pi·min-1·mg-1protein)。泽泻单体23-乙酰泽泻醇B、24-乙酰泽泻醇A均与P-gp有较强的相互作用,ATP酶动力学研究显示其Km值和Vmax值分别为0.79±0.28μM,2.01±0.67μM和50.57±3.72 nmol Pi·min-1·mg-1protein,56.28±29.6 nmol Pi·min-1·mg-1protein。结论:Fang-2与MDR1存在相互作用,其中泽泻为主要被MDR1转运的饮片,泽泻的有效组分23-乙酰泽泻醇B和24-乙酰泽泻醇A均是MDR1底物。表明该降脂中药与临床上其他降脂药物的联用时应充分考虑MDR1介导的转运行相互作用,为临床用降脂药物提供参考和依据。 展开更多
关键词 降脂中药 MDR1 体外 ATP酶分析法 转运性相互作用 泽泻 MDR1
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Correlation between inhibition of calcium-dependent apoptosis by cyclosporin A and calcium transportation in HL-60 cells 被引量:1
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作者 HUANG QI QING MING FANG +1 位作者 HONG QING ZHANG SHAO BAI XUE(Department of Biology, Beijing Normal University, Beijing 100875, China.) 《Cell Research》 SCIE CAS CSCD 1996年第1期23-30,共8页
Both calcium ionophore A23187 and endoplasmic reticulum Ca2+- ATPase inhibitor thapsigargin (Tg) could increase intracellular free calcium concentration and induce apoptosis in some cell lines. In the present study, w... Both calcium ionophore A23187 and endoplasmic reticulum Ca2+- ATPase inhibitor thapsigargin (Tg) could increase intracellular free calcium concentration and induce apoptosis in some cell lines. In the present study, we found that HL-60 cells treated with A23187 (1μg/ml) for 4 h or with Tg (0.5μg/ml) for 2 h showed typical characteristics of apoptosis. Pretreatment with nontoxic concentration of cyclosporin A (CsA) (1μg/ml) Could block these effects. Flow cytometric analysis of intracellular Ca2+ after staining with fluo-3 AM showed that CsA did not prevent the increase of intracellular calcium induced by A23187 or Tg, but it could maintain the high level of intracellular Ca2+ for a long time. These results suggest that CsA may prevent calcium- induced apoptosis by blocking the transportation of Ca2+ in HL-60cells. 展开更多
关键词 Cyclosporin A calcium ionophore A_(23187) THAPSIGARGIN APOPTOSIS intracellular calcium
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Detoxification of toxic herbs in TCM prescription based on modulation of efflux transporters
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作者 QIAN Liyunhe HE Yufei +1 位作者 ZHANG Mei XIE Ying 《Digital Chinese Medicine》 2021年第1期9-18,共10页
Traditional Chinese medicines(TCMs)have been used to prevent and treat various diseases for thousands of years.Promoting efficacy and reducing toxicity by the compatibility theory of TCMs has attracted increasing atte... Traditional Chinese medicines(TCMs)have been used to prevent and treat various diseases for thousands of years.Promoting efficacy and reducing toxicity by the compatibility theory of TCMs has attracted increasing attention,especially for the toxicity of herbs.Studies have pointed out the interactions between the active compounds of herbs and transporters in the detoxification process of toxic compounds.Here,we summarize data on five toxic herbs commonly used in TCMs and their related efflux transporters to reduce toxicity to offer a scientific rationale for the compatibility principle of TCMs and provide guidance for the rational clinical use of TCMs. 展开更多
关键词 Toxic herbs Efflux transporters DETOXIFICATION TCMs compatibility principles P-glycoprotein(P-gp)
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A Study on Antitoxic Role of Vesicular Monoamine Transporter 2 in Transgenic Chinese Hamster Overy Cells
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作者 叶民 丁新生 +2 位作者 董海蓉 仇镇宁 管晓虹 《Journal of Nanjing Medical University》 2003年第2期87-92,共6页
Objective : To study the antitoxic role of vesicular monoamine transporter 2 (VMAT2) in transgenic Chinese Hamster ovary (CHO) cell. Methods :With the technology of trans-gene from PC 12 to CHO, MTT reduction assay wa... Objective : To study the antitoxic role of vesicular monoamine transporter 2 (VMAT2) in transgenic Chinese Hamster ovary (CHO) cell. Methods :With the technology of trans-gene from PC 12 to CHO, MTT reduction assay was used to detect MPP+ toxic effect on wild type CHO (wtCHO) and transgenic CHO. Meanwhile, the role of reserpine was also observed in MPP+ toxic effects. Results :The sensitivity of transgenic CHO to MPP+ was much less than that of wtCHO with 0. 5 mmol/L MPP+. Transgenic CHO had the same sensitivity as wtCHO if rotenone was given. WtCHO, by given reserpine alone, didn't change its sensitivity to MPP+. Conclusions :VMAT2 has protective effect on transgenic CHO by transporting MPP+ to vesicles. 展开更多
关键词 transgenic Chinese Hamster Ovary Vesicular Monoamine Transporter 2 ANTITOXIC MPP+ RESERPINE
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Transfer RNA:A dancer between charging and mis-charging for protein biosynthesis 被引量:5
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作者 ZHOU XiaoLong WANG EnDuo 《Science China(Life Sciences)》 SCIE CAS 2013年第10期921-932,共12页
Transfer RNA plays a fundamental role in the protein biosynthesis as an adaptor molecule by functioning as a biological link between the genetic nucleotide sequence in the mRNA and the amino acid sequence in the prote... Transfer RNA plays a fundamental role in the protein biosynthesis as an adaptor molecule by functioning as a biological link between the genetic nucleotide sequence in the mRNA and the amino acid sequence in the protein.To perform its role in protein biosynthesis,it has to be accurately recognized by aminoacyl-tRNA synthetases(aaRSs)to generate aminoacyl-tRNAs(aa-tRNAs).The correct pairing between an amino acid with its cognate tRNA is crucial for translational quality control.Production and utilization of mis-charged tRNAs are usually detrimental for all the species,resulting in cellular dysfunctions.Correct aa-tRNAs formation is collectively controlled by aaRSs with distinct mechanisms and/or other trans-factors.However,in very limited instances,mis-charged tRNAs are intermediate for specific pathways or essential components for the translational machinery.Here,from the point of accuracy in tRNA charging,we review our understanding about the mechanism ensuring correct aa-tRNA generation.In addition,some unique mis-charged tRNA species necessary for the organism are also briefly described. 展开更多
关键词 TRNA aminoacyl-tRNA synthetase AMINOACYLATION EDITING
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Interaction of δ-opioid Receptor with Membrane Transporters: Possible Mechanisms in Pain Suppression by Acupuncture 被引量:17
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作者 杨智杰 鲍国斌 +6 位作者 邓海平 杜慧明 顾全保 裴钢 濮璐 Wolfgang SCHWARZ 夏鹏 《Journal of Acupuncture and Tuina Science》 2008年第5期298-300,共3页
Objective: To investigate the possible mechanisms in acupuncture analgesia by interaction of δ-opioid receptor with neurotransmitter transport proteins or the Na^+-K^+ pump. Methods: Microinjection of respective ... Objective: To investigate the possible mechanisms in acupuncture analgesia by interaction of δ-opioid receptor with neurotransmitter transport proteins or the Na^+-K^+ pump. Methods: Microinjection of respective heterologous cRNA into the Xenopus oocytes as a model system, and measurement of steady-state currents under two-electrode voltage clamp. Results: The co-expression of the 8-opioid receptor with GAT1, EAAC 1 or the sodium pump resulted in reducing activity of the respective transporter. Opioid receptor activation affected transporter activity in different ways: 1) GAT1 was further inhibited; 2) EAAC1 was stimulated; 3) Na^+-K^+ pump activity interfered with agonist sensitivity of DOR. Pump inhibition led to higher sensitivity for DPDPE. Conclusion: GABA transporter inhibition and glutamate transporter stimulation may counteract pain sensation by affecting the neurotransmitter concentration in the synaptic cleft and, therefore, may contribute synergistically to pain suppression by acupuncture. Sodium pump inhibition by endogenous ouabain may amplify these effects. These synergistic effects may be the molecular mechanism of inhibiting pain sense and/or acupuncture analgesia. 展开更多
关键词 Acupuncture Analgesia Receptors Opioid Neurotransmitter Transport Proteins Protein Interaction Domains and Motifs
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Protective effect of liposome-mediated glial cell line-derived neurotrophic factor gene transfer in vivo on motoneurons following spinal cord injury in rats 被引量:6
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作者 鲁凯伍 陈哲宇 侯铁胜 《Chinese Journal of Traumatology》 CAS 2004年第5期275-279,共5页
Objective: To investigate the effect of liposome-mediated glial cell line-derived neurotrophic factor (GDNF) gene transfer in vivo on spinal cord motoneurons after spinal cord injury (SCI) in adult rats. Methods: Sixt... Objective: To investigate the effect of liposome-mediated glial cell line-derived neurotrophic factor (GDNF) gene transfer in vivo on spinal cord motoneurons after spinal cord injury (SCI) in adult rats. Methods: Sixty male Sprague-Dawley rats were divided equally into two groups: GDNF group and control group. The SCI model was established according to the method of Nystrom, and then the DC-Chol liposomes and recombinant plasmid pEGFP-GDNF cDNA complexes were injected into the injured spinal cord. The expression of GDNF cDNA 1 week after injection was detected by RT-PCR and fluorescence microscope. We observed the remaining motoneurons in the anterior horn and the changes of cholinesterase (CHE) and acid phosphatase (ACP) activity using Nissl and enzyme histochemistry staining. The locomotion function of hind limbs of rats was evaluated using inclined plane test and BBB locomotor scale. Results: RT-PCR and fluorescence observation confirmed the presence of expression of GDNF cDNA 1 week and 4 weeks after injection. At 1, 2, 4 weeks after SCI, the number of motoneurons in the anterior horn in GDNF group ((20.4)±(3.2), (21.7)±(3.6), (22.5)±(3.4)) was more than that in control group ((16.8)±(2.8), (17.3)±(2.7), (18.2)±(3.2), P<(0.05)). At 1, 2 weeks after SCI, the mean gray of the CHE-stained spinal motoneurons in GDNF group ((74.2)±(25.8), (98.7)±(31.6)) was less than that in control group ((98.5)±(32.2), (134.6)±(45.2), P<(0.01)), and the mean gray of ACP in GDNF group ((84.5)±(32.6), (79.5)±(28.4)) was more than that in control group ((61.2)±(24.9), (52.6)±(19.9), P<(0.01)). The locomotion functional scales in GDNF group were higher than that in control group within 1 to 4 weeks after SCI (P<(0.05)). Conclusions: GDNF gene transfer in vivo can protect motoneurons from death and degeneration induced by incompleted spinal cord injury as well as enhance locomotion functional restoration of hind limbs. These results suggest that liposome-mediated delivery of GDNF cDNA might be a practical method for treating traumatic spinal cord injury. 展开更多
关键词 Spinal cord injury Motor neurons LIPOSOME Gene therapy
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Spin manipulations through electrical and thermoelectrical transport in magnetic tunnel junctions 被引量:1
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作者 ZHU ZhenGang SU Gang 《Science China(Physics,Mechanics & Astronomy)》 SCIE EI CAS 2013年第1期166-183,共18页
A brief review is presented,which includes the direct current,alternate current,electrical and thermoelectrical transport as well as spin transfer effect in a variety of spin-based nanostructures such as the magnetic ... A brief review is presented,which includes the direct current,alternate current,electrical and thermoelectrical transport as well as spin transfer effect in a variety of spin-based nanostructures such as the magnetic tunnel junction(MTJ),ferromagnet(FM)-quantum dot(QD)/FM-FM,double barrier MTJ,FM-marginal Fermi liquid-FM,FM-unconventional superconductor-FM(FUSF),quantum ring and optical spin-field-effect transistor.The magnetoresistances in those structures,spin accumulation effect in FM-QD-FM and FUSF systems,spin injection and spin filter into semiconductor,spin transfer effect,photon-assisted spin transport,magnonassisted tunneling,electron-electron interaction effect on spin transport,laser-controlled spin dynamics,and thermoelectrical spin transport are discussed. 展开更多
关键词 SPINTRONICS magnetic tunnel junction spin transport MAGNETORESISTANCE spin transfer torque spin injection spin filter SPIN-VALVE SPIN-ORBIT
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