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We are analyzing https://link.springer.com/article/10.1007/s11010-014-2090-7.

Title:
Rapamycin promotes podocyte autophagy and ameliorates renal injury in diabetic mice | Molecular and Cellular Biochemistry
Description:
The aim was to explore the effects of rapamycin on autophagy and injury of podocytes in streptozocin (STZ)-induced type 1 diabetic mice, and its role in delaying progression of diabetic nephropathy. In this study, male Balb/c mice were divided into three groups: control (n = 12), STZ-induced diabetic (n = 12), and rapamycin-treated diabetic (DM + Rapa) (n = 12), which received intraperitoneal injection of rapamycin (2 mg/kg/48 h) after induction of DM. Levels of urinary albumin (UA), blood urea nitrogen, serum creatinine, and kidney weight/body weight were measured at week 12. Renal pathologic changes, number of podocytes autophagy, and organelles injury were investigated by PAS staining, transmission electron microscopy, and immunofluorescence staining, respectively. Western blot was performed to determine the expression of LC3 (a podocyte autophagy marker), phosphorylated mammalian target of rapamycin, p-p70S6K, bax, and caspase-3 protein. Podocytes count was evaluated by immunofluorescence staining and Wilms tumor 1 immunohistochemistry, and Western blot of nephrin and podocin. The results indicated that rapamycin could reduce the kidney weight/body weight and UA secretion. It could alleviate podocyte foot process fusion, glomerular basement membrane thickening, and matrix accumulation, and increase the number of autophagosomes, and LC3-expressing podocytes. Down-regulation of bax and caspase-3 protein, and up-regulation of nephrin and podocin protein were observed in the glomeruli of diabetic mice after administration of rapamycin. In conclusion, rapamycin can ameliorate renal injury in diabetic mice by increasing the autophagy activity and inhibition of apoptosis of podocytes.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {šŸ“š}

  • Education
  • Health & Fitness
  • Science

Content Management System {šŸ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {šŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {šŸ’ø}

We don't see any clear sign of profit-making.

Not every website is profit-driven; some are created to spread information or serve as an online presence. Websites can be made for many reasons. This could be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {šŸ”}

article, google, scholar, pubmed, diabetic, cas, rapamycin, nephropathy, autophagy, podocyte, injury, kidney, mice, wang, zhao, cell, podocytes, renal, diabetes, central, guan, access, disease, mol, biochem, mtor, privacy, cookies, content, type, glomerular, liu, development, nephrol, publish, research, search, ameliorates, huang, yang, progression, cells, int, rats, clin, chen, china, function, data, information,

Topics {āœ’ļø}

month download article/chapter hyperglycemia-induced podocyte injury ampkα-regulated autophagy induction kidney weight/body weight related subjects cellular biochemistry aims full article pdf growth signal integration podocyte autophagy marker privacy choices/manage cookies pi3k-induced stat1/3 stz-induced diabetic received intraperitoneal injection experimental diabetic nephropathy glomerular epithelial cells oxidative stress parameters chronic allograft nephropathy diabetic renal injury rapamycin-treated diabetic ameliorates renal injury diabetic kidney disease ghrl gene prevents maintains podocyte homeostasis hepg2 hepatocyte cells mtor pathway article xiao check access instant access article molecular ameliorate renal injury european economic area ke yang transmission electron microscopy single intravenous injection asians versus whites phosphatidylinositol kinase homologue usf1 transcription factor shu-chien ac strong therapeutic potential wiggins rc proteinuric experimental nephropathies military medical university conditions privacy policy de cavaglieri cassia article log de azevedo mj accepting optional cookies diabetic rats treated blood urea nitrogen parving hh

Questions {ā“}

  • Baehrecke EH (2005) Autophagy: dual roles in life and death?
  • Lasaridis AN, Sarafidis PA (2003) Diabetic nephropathy and antihypertensive treatment: what are the lessons from clinical trials?
  • Lu MK, Gong XG, Guan KL (2011) mTOR in podocyte function: is rapamycin good for diabetic nephropathy?
  • Skoberne A, Konieczny A, Schiffer M (2009) Glomerular epithelial cells in the urine: what has to be done to make them worthwhile?
  • Torras J, Herrero-Fresneda I, Gulias O, Flaguer M, Vidal A, Cruzado JM, Lioberas N, Franguesa MI, Grinyo JM (2009) Rapamycin has dual opposing effects on proteinuric experimental nephropathies: is it a matter of podocyte damage?

Schema {šŸ—ŗļø}

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         headline:Rapamycin promotes podocyte autophagy and ameliorates renal injury in diabetic mice
         description:The aim was to explore the effects of rapamycin on autophagy and injury of podocytes in streptozocin (STZ)-induced type 1 diabetic mice, and its role in delaying progression of diabetic nephropathy. In this study, male Balb/c mice were divided into three groups: control (nĀ =Ā 12), STZ-induced diabetic (nĀ =Ā 12), and rapamycin-treated diabetic (DMĀ +Ā Rapa) (nĀ =Ā 12), which received intraperitoneal injection of rapamycin (2Ā mg/kg/48Ā h) after induction of DM. Levels of urinary albumin (UA), blood urea nitrogen, serum creatinine, and kidney weight/body weight were measured at week 12. Renal pathologic changes, number of podocytes autophagy, and organelles injury were investigated by PAS staining, transmission electron microscopy, and immunofluorescence staining, respectively. Western blot was performed to determine the expression of LC3 (a podocyte autophagy marker), phosphorylated mammalian target of rapamycin, p-p70S6K, bax, and caspase-3 protein. Podocytes count was evaluated by immunofluorescence staining and Wilms tumor 1 immunohistochemistry, and Western blot of nephrin and podocin. The results indicated that rapamycin could reduce the kidney weight/body weight and UA secretion. It could alleviate podocyte foot process fusion, glomerular basement membrane thickening, and matrix accumulation, and increase the number of autophagosomes, and LC3-expressing podocytes. Down-regulation of bax and caspase-3 protein, and up-regulation of nephrin and podocin protein were observed in the glomeruli of diabetic mice after administration of rapamycin. In conclusion, rapamycin can ameliorate renal injury in diabetic mice by increasing the autophagy activity and inhibition of apoptosis of podocytes.
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            Cancer Research
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      headline:Rapamycin promotes podocyte autophagy and ameliorates renal injury in diabetic mice
      description:The aim was to explore the effects of rapamycin on autophagy and injury of podocytes in streptozocin (STZ)-induced type 1 diabetic mice, and its role in delaying progression of diabetic nephropathy. In this study, male Balb/c mice were divided into three groups: control (nĀ =Ā 12), STZ-induced diabetic (nĀ =Ā 12), and rapamycin-treated diabetic (DMĀ +Ā Rapa) (nĀ =Ā 12), which received intraperitoneal injection of rapamycin (2Ā mg/kg/48Ā h) after induction of DM. Levels of urinary albumin (UA), blood urea nitrogen, serum creatinine, and kidney weight/body weight were measured at week 12. Renal pathologic changes, number of podocytes autophagy, and organelles injury were investigated by PAS staining, transmission electron microscopy, and immunofluorescence staining, respectively. Western blot was performed to determine the expression of LC3 (a podocyte autophagy marker), phosphorylated mammalian target of rapamycin, p-p70S6K, bax, and caspase-3 protein. Podocytes count was evaluated by immunofluorescence staining and Wilms tumor 1 immunohistochemistry, and Western blot of nephrin and podocin. The results indicated that rapamycin could reduce the kidney weight/body weight and UA secretion. It could alleviate podocyte foot process fusion, glomerular basement membrane thickening, and matrix accumulation, and increase the number of autophagosomes, and LC3-expressing podocytes. Down-regulation of bax and caspase-3 protein, and up-regulation of nephrin and podocin protein were observed in the glomeruli of diabetic mice after administration of rapamycin. In conclusion, rapamycin can ameliorate renal injury in diabetic mice by increasing the autophagy activity and inhibition of apoptosis of podocytes.
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      dateModified:2014-05-22T00:00:00Z
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         Rapamycin
         Podocyte injury
         Autophagy
         mTOR signal pathway
         Diabetic nephropathy
         Biochemistry
         general
         Cardiology
         Cancer Research
         Medical Biochemistry
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            name:Ling Nie
            affiliation:
                  name:Third Military Medical University
                  address:
                     name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Song Wang
            affiliation:
                  name:Third Military Medical University
                  address:
                     name:State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury of PLA, Third Military Medical University, Chongqing, People’s Republic of China
                     type:PostalAddress
                  type:Organization
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                  name:Third Military Medical University
                  address:
                     name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
                     type:PostalAddress
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                     type:PostalAddress
                  type:Organization
            type:Person
            name:Junping Wang
            affiliation:
                  name:Third Military Medical University
                  address:
                     name:State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury of PLA, Third Military Medical University, Chongqing, People’s Republic of China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jinghong Zhao
            affiliation:
                  name:Third Military Medical University
                  address:
                     name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
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      name:Ling Nie
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               type:PostalAddress
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      name:Song Wang
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            name:Third Military Medical University
            address:
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      name:Lei Sun
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            name:Third Military Medical University
            address:
               name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
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      name:Ting He
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            name:Third Military Medical University
            address:
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      name:Yunjian Huang
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            name:Third Military Medical University
            address:
               name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
               type:PostalAddress
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      name:Jingbo Zhang
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            name:Third Military Medical University
            address:
               name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
               type:PostalAddress
            type:Organization
      name:Ke Yang
      affiliation:
            name:Third Military Medical University
            address:
               name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
               type:PostalAddress
            type:Organization
      name:Junping Wang
      affiliation:
            name:Third Military Medical University
            address:
               name:State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury of PLA, Third Military Medical University, Chongqing, People’s Republic of China
               type:PostalAddress
            type:Organization
      name:Jinghong Zhao
      affiliation:
            name:Third Military Medical University
            address:
               name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury of PLA, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
      name:State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury of PLA, Third Military Medical University, Chongqing, People’s Republic of China
      name:Department of Nephrology, Institute of Nephrology of Chongqing and Kidney Center of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, People’s Republic of China
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