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The miR-9-5p/CXCL11 pathway is a key target of hydrogen sulfide-mediated inhibition of neuroinflammation in hypoxic ischemic brain injury 被引量:2
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作者 Yijing Zhao Tong Li +6 位作者 Zige Jiang Chengcheng Gai Shuwen Yu Danqing Xin Tingting Li Dexiang Liu Zhen Wang 《Neural Regeneration Research》 SCIE CAS CSCD 2024年第5期1084-1091,共8页
We previously showed that hydrogen sulfide(H2S)has a neuroprotective effect in the context of hypoxic ischemic brain injury in neonatal mice.However,the precise mechanism underlying the role of H2S in this situation r... We previously showed that hydrogen sulfide(H2S)has a neuroprotective effect in the context of hypoxic ischemic brain injury in neonatal mice.However,the precise mechanism underlying the role of H2S in this situation remains unclear.In this study,we used a neonatal mouse model of hypoxic ischemic brain injury and a lipopolysaccharide-stimulated BV2 cell model and found that treatment with L-cysteine,a H2S precursor,attenuated the cerebral infarction and cerebral atrophy induced by hypoxia and ischemia and increased the expression of miR-9-5p and cystathionineβsynthase(a major H2S synthetase in the brain)in the prefrontal cortex.We also found that an miR-9-5p inhibitor blocked the expression of cystathionineβsynthase in the prefrontal cortex in mice with brain injury caused by hypoxia and ischemia.Furthermore,miR-9-5p overexpression increased cystathionine-β-synthase and H2S expression in the injured prefrontal cortex of mice with hypoxic ischemic brain injury.L-cysteine decreased the expression of CXCL11,an miR-9-5p target gene,in the prefrontal cortex of the mouse model and in lipopolysaccharide-stimulated BV-2 cells and increased the levels of proinflammatory cytokines BNIP3,FSTL1,SOCS2 and SOCS5,while treatment with an miR-9-5p inhibitor reversed these changes.These findings suggest that H2S can reduce neuroinflammation in a neonatal mouse model of hypoxic ischemic brain injury through regulating the miR-9-5p/CXCL11 axis and restoringβ-synthase expression,thereby playing a role in reducing neuroinflammation in hypoxic ischemic brain injury. 展开更多
关键词 chemokine(C-X-C motif)ligand 11 cystathionineβsynthase H2S hypoxic ischemic brain injury inflammation L-CYSTEINE lipopolysaccharide microglia miR-9-5p neuroprotection
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Pectate lyase is a factor in the adaptability for Heterodera glycines infecting tobacco 被引量:2
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作者 TIAN Zhong-ling SHI Hong-li +1 位作者 Munawar Maria ZHENG Jing-wu 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2019年第3期618-626,共9页
The soybean cyst nematode, Heterodeara glycines, is a serious pathogen of soybean, and reported to be the host of a wide range of Fabaceae. In the present study, the host specificity and reproductivity of two populati... The soybean cyst nematode, Heterodeara glycines, is a serious pathogen of soybean, and reported to be the host of a wide range of Fabaceae. In the present study, the host specificity and reproductivity of two populations of H. glycines collected from soybean and tobacco were identified and characterized. The comparative identity between β-1,4-endoglucanase, pectate lyase and chorismate mutase of H. glycines parasitizing on soybean and tobacco were 99, 97 and 98%, respectively. The qR T-PCR analysis indicated that the expression of pectate lyase 2 gene was significantly higher in second-stage juveniles of H. glycines Henan population parasitizing on tobacco than that of H. glycines Shanxi population parasitizing on soybean. In addition, the pectic acid content of cell wall was significantly higher(45%) in the roots of tobacco than the roots of soybean. Our results indicate that the changes in transcript parasitism genes may be a result of long-term evolution illustrating how a plant-parasitic nematode adapts to the host environment for optimal infestation and survival. 展开更多
关键词 s: HETERODERA GLYCINES TOBACCO parasitism genes β-1 4-endoglucanase pectate lyase CHORISMATE mutase pectic acid
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Formation of (2E)-4-Hydroxy-2-nonenal and (2E)-4-Hydroxy-2-hexenal by Plant Enzymes: A Review Suggests a Role in the Physiology of Plants
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作者 Harold W. Gardner 《Advances in Enzyme Research》 CAS 2016年第2期56-61,共6页
It is demonstrated that (3Z)-nonenal (NON) and (3Z)-hexenal (HEX) are oxidized in a cascade by lipoxygenase (LOX) and hydroperoxide peroxygenase (HP peroxygenase) into (2E)-4-hydroxy-2- nonenal (HNE) and (2E)-4-hydrox... It is demonstrated that (3Z)-nonenal (NON) and (3Z)-hexenal (HEX) are oxidized in a cascade by lipoxygenase (LOX) and hydroperoxide peroxygenase (HP peroxygenase) into (2E)-4-hydroxy-2- nonenal (HNE) and (2E)-4-hydroxy-2-hexenal (HHE), respectively. In turn, HNE inactivates LOX terminating the cascade. The hydroxy-alkenals produced serve to inhibit plant pathogens, which initiated the cascade. In addition to LOX, other unknown oxygenases may be involved in the cascade. 展开更多
关键词 (3Z)-Nonenal (3Z)-Hexenal (2E)-4-Hydroxy-2-nonenal (2E)-4-Hydroxy-2-hexenal (2E)-4-Hydroperoxy-2-hexenal LIPOXYGENASE Hydroperoxide Peroxygenase Hydroperoxide lyase (2E)-4-Hydroperoxy-2-Nonenal 3 4-Epoxynonanal (2E)-4-Oxo-2-nonenal Glycine max Vica faba Plant Pathogen
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同型半胱氨酸与甲基代谢及其胱硫醚酶基因研究进展 被引量:3
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作者 农茜 陆文权 +2 位作者 梁烨 赖腾芳 李天资 《临床医学进展》 2020年第7期1277-1284,共8页
同型半胱氨酸(HCY)水平增高是慢性血管疾病的独立危险因子,但HCY的来源不是从食物中吸取,其由蛋氨酸在甲基(CH3)循环代谢的中间产物。甲基化代谢亢进,再甲基化或转硫化代谢酶基因突变或功能障碍等原因均可造成甲基循环代谢失衡,从而导致... 同型半胱氨酸(HCY)水平增高是慢性血管疾病的独立危险因子,但HCY的来源不是从食物中吸取,其由蛋氨酸在甲基(CH3)循环代谢的中间产物。甲基化代谢亢进,再甲基化或转硫化代谢酶基因突变或功能障碍等原因均可造成甲基循环代谢失衡,从而导致HCY推积,患者出现高同型半胱氨酸血症(HHCY),动脉硬化等为特征的临床症状和体征。胱硫醚β-合酶(CBS)基因可将HCY转硫化成为胱硫醚,后者再经过胱硫醚-γ-裂解酶(CTH)裂解成丙酮酸、硫酸和水,达到有效降低HCY水平,降低动脉硬化进展,保障机体健康。本文综述近年来HCY代谢通路及其与心血管疾病的关系等的研究许多新进展。 展开更多
关键词 高同型半胱氨酸血症 甲基代谢 胱硫醚β-合酶(cystathionase CBS) 胱硫醚-裂解酶(cystathionine gamma-lyase CTH) 动脉硬化
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