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In vitro assessment of gastrointestinal viability of two photosynthetic bacteria,Rhodopseudomonas palustris and Rhodobacter sphaeroides 被引量:4
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作者 ZHOU Xu-xia PAN Yuan-jiang +1 位作者 WANG Yan-bo LI Wei-fen 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2007年第9期686-692,共7页
The objectives of this study were to assess the potential of two photosynthetic bacteria (PSB), Rhodopseudomonas palustris HZ0301 and Rhodobacter sphaeroides HZ0302, as probiotics in aquaculture. The viability of HZ... The objectives of this study were to assess the potential of two photosynthetic bacteria (PSB), Rhodopseudomonas palustris HZ0301 and Rhodobacter sphaeroides HZ0302, as probiotics in aquaculture. The viability of HZ0301 and HZ0302 in simulated gastric transit conditions (pH 2.0, pH 3.0 and pH 4.0 gastric juices) and in simulated small intestinal transit conditions (pH 8.0, with or without 0.3% bile salts) was tested. The effects of HZ0301 and HZ0302 on the viability and permeability of intestinal epithelial cell in primary culture of tilapias, Oreochrornis nilotica, were also detected. All the treatments were deter- mined with three replicates. The simulated gastric transit tolerance of HZ0301 and HZ0302 strains was pH-dependent and correspondingly showed lower viability at pH 2.0 after 180 min compared with pH 3.0 and pH 4.0. Both HZ0301 and HZ0302 were tolerant to simulated small intestine transit with or without bile salts in our research. Moreover, there was no significant difference (P〉0.05) among three treatments including the control and the groups treated with HZ0301 or HZ0302 both in intestinal epithelial cell viability and membrane permeability, showing no cell damage. In summary, this study demonstrated that HZ0301 and HZ0302 had high capacity of upper gastrointestinal transit tolerance and were relatively safe for intestinal epithelial cells of tilapias. 展开更多
关键词 Photosynthetic bacteria PROBIOTICS Primary culture Intestinal epithelial cell Oreochromis nilotica
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Developments in metastatic pancreatic cancer:Is gemcitabine still the standard? 被引量:3
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作者 Jie-Er Ying Li-Ming Zhu Bi-Xia Liu 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第8期736-745,共10页
In the past 15 years, we have seen few therapeutic advances for patients with pancreatic cancer, which is the fourth leading cause of cancer-related death in the United States. Currently, only about 6% of patients wit... In the past 15 years, we have seen few therapeutic advances for patients with pancreatic cancer, which is the fourth leading cause of cancer-related death in the United States. Currently, only about 6% of patients with advanced disease respond to standard gemcitabine therapy, and median survival is only about 6 mo. Moreover, phase Ⅲ trials have shown that adding various cytotoxic and targeted chemotherapeutic agents to gemcitabine has failed to improve overall survival, except in cases in which gemcitabine combined with erlotinib show minimal survival benefi t. Several metaanalyses have shown that the combination of gemcitabine with either a platinum analog or capecitabine may lead to clinically relevant survival prolongation, especially for patients with good performance status. Meanwhile, many studies have focused on the pharmacokinetic modulation of gemcitabine by fi xed-dose administration, and metabolic or transport enzymes related to the response and toxicity of gemcitabine. Strikingly, a phase Ⅲ trial in 2010 showed that, in comparison to gemcitabine alone, the FOLFIRINOX regimen in patients with advanced disease and good performance status, produced better median overall survival, median progression-free survival, and objective response rates. This regimen also resulted in greater, albeit manageable toxicity. 展开更多
关键词 CHEMOTHERAPY Palliative therapy Metasta-sis Biomarkers Pancreatic neoplasms
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过表达C3G对高糖诱导H9C2心肌细胞增殖和凋亡的影响 被引量:1
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作者 张旭 陈旺盛 +2 位作者 张梦娇 聂娇 陈秀 《重庆医学》 CAS 2018年第8期1033-1035,共3页
目的探讨过表达C3G对高糖诱导H9C2心肌细胞增殖和凋亡的影响。方法分别用pCXN2-Flag(空质粒)、pCXN2-Flag-hC3G(人过表达C3G mRNA)质粒通过瞬时转染H9C2心肌细胞,并进行高糖干预。实验分为空白组、空载体组、过表达C3G组、空白+高糖组... 目的探讨过表达C3G对高糖诱导H9C2心肌细胞增殖和凋亡的影响。方法分别用pCXN2-Flag(空质粒)、pCXN2-Flag-hC3G(人过表达C3G mRNA)质粒通过瞬时转染H9C2心肌细胞,并进行高糖干预。实验分为空白组、空载体组、过表达C3G组、空白+高糖组、空载体+高糖组、过表达C3G+高糖组,分别检测各组H9C2心肌细胞的C3G蛋白表达、增殖率及凋亡率。结果空白+高糖组、空载体+高糖组较空白组、空载体组细胞增殖率均明显降低,凋亡率均明显升高。过表达C3G组较空白组与空载体组,过表达C3G+高糖组较空白+高糖组与空载体+高糖组H9C2心肌细胞的C3G蛋白表达增加,增殖率升高,凋亡率明显降低。结论高糖抑制H9C2心肌细胞增殖、促进H9C2心肌细胞凋亡;过表达C3G可逆转高糖诱导H9C2心肌细胞增殖率的降低、凋亡率的升高。过表达C3G能促进高糖诱导H9C2心肌细胞的生存力。 展开更多
关键词 H9C2心肌细胞 鸟嘌呤核苷酸释放因子2 高糖血症 细胞生存力
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