Sulfonylureas are widely used oral anti-diabetic drugs.However,its long-term usage effects on patients’lifespan remain controversial,with no reports of influence on animal longevity.Hence,the anti-aging effects of ch...Sulfonylureas are widely used oral anti-diabetic drugs.However,its long-term usage effects on patients’lifespan remain controversial,with no reports of influence on animal longevity.Hence,the anti-aging effects of chlorpropamide along with glimepiride,glibenclamide,and tolbutamide were studied with special emphasis on the interaction of chlorpropamide with mitochondrial ATP-sensitive K+(mito K-ATP)channels and mitochondrial complex II.Chlorpropamide delayed aging in Caenorhabditis elegans,human lung fibroblast MRC-5 cells and reduced doxorubicin-induced senescence in both MRC-5 cells and mice.In addition,the mitochondrial membrane potential and ATP levels were significantly increased in chlorpropamide-treated worms,which is consistent with the function of its reported targets,mito K-ATP channels.Increased levels of mitochondrial reactive oxygen species(mt ROS)were observed in chlorpropamide-treated worms.Moreover,the lifespan extension by chlorpropamide required complex II and increased mt ROS levels,indicating that chlorpropamide acts on complex II directly or indirectly via mito K-ATP to increase the production of mt ROS as a pro-longevity signal.This study provides mechanistic insight into the anti-aging effects of sulfonylureas in C.elegans.展开更多
The theoretical study of chlorpropamide, tolazamide and glipizide was carried out by the </span><span style="font-family:Verdana;">Density Functional Theory </span><span style="font...The theoretical study of chlorpropamide, tolazamide and glipizide was carried out by the </span><span style="font-family:Verdana;">Density Functional Theory </span><span style="font-family:Verdana;">(DFT) at B3LYP/6-31G(d) level. This study</span></span><span style="font-family:""> </span><span style="font-family:Verdana;">made it possible to determine the global reactivity parameters in order to better understand the interactions between the molecules studied and the copper surface. Then, the determination of local reactivity indices (Fukui functions and dual descriptor) on these molecules resulted in the precision </span><span style="font-family:Verdana;">on </span><span style="font-family:Verdana;">the most probable center</span><span style="font-family:Verdana;">s </span><span style="font-family:Verdana;">of nucleophilic and electrophilic attacks within each molecule. The results obtained, show that chloropropamide, tolazamide and glipizide can be good inhibitors against copper corrosion. Thus, the mechanism of copper corrosion inhibition of these compounds in nitric acid solution has been explained </span><span style="font-family:Verdana;">by means of theoretical calculations</span><span style="font-family:Verdana;">.展开更多
基金Financial support for this research provided by the National Natural Science Foundation of China(22037002 and 81772689)the Program for Professor of Special Appointment(Eastern Scholar TP2018025,China)at Shanghai Institutions of Higher Learning+2 种基金the Innovative Research Team of High-level Local Universities in Shanghaithe Chinese Special Fund for State Key Laboratory of Bioreactor Engineering(2060204,China)Strains of Caenorhabditis elegans were provided by the CGC,which is funded by NIH Office of Research Infrastructure Programs(P40 OD010440)。
文摘Sulfonylureas are widely used oral anti-diabetic drugs.However,its long-term usage effects on patients’lifespan remain controversial,with no reports of influence on animal longevity.Hence,the anti-aging effects of chlorpropamide along with glimepiride,glibenclamide,and tolbutamide were studied with special emphasis on the interaction of chlorpropamide with mitochondrial ATP-sensitive K+(mito K-ATP)channels and mitochondrial complex II.Chlorpropamide delayed aging in Caenorhabditis elegans,human lung fibroblast MRC-5 cells and reduced doxorubicin-induced senescence in both MRC-5 cells and mice.In addition,the mitochondrial membrane potential and ATP levels were significantly increased in chlorpropamide-treated worms,which is consistent with the function of its reported targets,mito K-ATP channels.Increased levels of mitochondrial reactive oxygen species(mt ROS)were observed in chlorpropamide-treated worms.Moreover,the lifespan extension by chlorpropamide required complex II and increased mt ROS levels,indicating that chlorpropamide acts on complex II directly or indirectly via mito K-ATP to increase the production of mt ROS as a pro-longevity signal.This study provides mechanistic insight into the anti-aging effects of sulfonylureas in C.elegans.
文摘The theoretical study of chlorpropamide, tolazamide and glipizide was carried out by the </span><span style="font-family:Verdana;">Density Functional Theory </span><span style="font-family:Verdana;">(DFT) at B3LYP/6-31G(d) level. This study</span></span><span style="font-family:""> </span><span style="font-family:Verdana;">made it possible to determine the global reactivity parameters in order to better understand the interactions between the molecules studied and the copper surface. Then, the determination of local reactivity indices (Fukui functions and dual descriptor) on these molecules resulted in the precision </span><span style="font-family:Verdana;">on </span><span style="font-family:Verdana;">the most probable center</span><span style="font-family:Verdana;">s </span><span style="font-family:Verdana;">of nucleophilic and electrophilic attacks within each molecule. The results obtained, show that chloropropamide, tolazamide and glipizide can be good inhibitors against copper corrosion. Thus, the mechanism of copper corrosion inhibition of these compounds in nitric acid solution has been explained </span><span style="font-family:Verdana;">by means of theoretical calculations</span><span style="font-family:Verdana;">.