Liver-targeted Nano-MitoPBN normalizes glucose metabolism by improving mitochondrial redox balance. (November 2019)
- Record Type:
- Journal Article
- Title:
- Liver-targeted Nano-MitoPBN normalizes glucose metabolism by improving mitochondrial redox balance. (November 2019)
- Main Title:
- Liver-targeted Nano-MitoPBN normalizes glucose metabolism by improving mitochondrial redox balance
- Authors:
- Wu, Meiling
Liao, Lihao
Jiang, Lihan
Zhang, Chunwang
Gao, Hongyang
Qiao, Liang
Liu, Shanlin
Shi, Dongyun - Abstract:
- Abstract: Recent advances in Nanomedicine provide promising disease treatment through improved drug delivery efficiency, but clinical applications have encountered difficulties, largely due to the majority of injected nanoparticle is sequestered in liver. In contrast, liver cells seem to be a perfect target for nanoparticles. Here we generated a new formula of liposome encapsulated Nano-MitoPBN as a liver mitochondrial-targeting free radical scavenger. We found that Nano-MitoPBN mainly accumulated in hepatocytes and scavenged hepatic mitochondrial superoxide/hydrogen peroxide generated from mono-electron leak of electron transport chain (ETC) complex I and III. Due to micro-compartmentalization, Nano-MitoPBN increased mitochondrial state 3 respiratory rate and respiratory control ratio (RCR), resulting in decreased NADH:NAD + ratio, improved mitochondrial oxidative energy coupling and ATP synthesis, thus alleviating ROS-induced mitochondrial dysfunction. The functional mitochondria promoted the substrate oxidation by the liver, resulting in increased glycolysis and TCA cycle, which directly speeds glucose decomposition, thus decreasing the peripheral blood glucose level and improving the impaired glucose tolerance in diabetic animals. Our study suggests the potential of liver mitochondrial targeting antioxidative nanomedicines for diabetes mellitus. Graphical abstract: Image 1 Highlights: Liposome encapsulated Nano-MitoPBN is used in liver-targeted therapy. Nano-MitoPBNAbstract: Recent advances in Nanomedicine provide promising disease treatment through improved drug delivery efficiency, but clinical applications have encountered difficulties, largely due to the majority of injected nanoparticle is sequestered in liver. In contrast, liver cells seem to be a perfect target for nanoparticles. Here we generated a new formula of liposome encapsulated Nano-MitoPBN as a liver mitochondrial-targeting free radical scavenger. We found that Nano-MitoPBN mainly accumulated in hepatocytes and scavenged hepatic mitochondrial superoxide/hydrogen peroxide generated from mono-electron leak of electron transport chain (ETC) complex I and III. Due to micro-compartmentalization, Nano-MitoPBN increased mitochondrial state 3 respiratory rate and respiratory control ratio (RCR), resulting in decreased NADH:NAD + ratio, improved mitochondrial oxidative energy coupling and ATP synthesis, thus alleviating ROS-induced mitochondrial dysfunction. The functional mitochondria promoted the substrate oxidation by the liver, resulting in increased glycolysis and TCA cycle, which directly speeds glucose decomposition, thus decreasing the peripheral blood glucose level and improving the impaired glucose tolerance in diabetic animals. Our study suggests the potential of liver mitochondrial targeting antioxidative nanomedicines for diabetes mellitus. Graphical abstract: Image 1 Highlights: Liposome encapsulated Nano-MitoPBN is used in liver-targeted therapy. Nano-MitoPBN efficiently scavenges hepatic mitochondrial respiratory-originated ROS. Nano-MitoPBN improves respiration and prevents mitochondrial dysfunction. Nano-MitoPBN increases glycolysis and aerobic oxidation in liver. … (more)
- Is Part Of:
- Biomaterials. Volume 222(2019)
- Journal:
- Biomaterials
- Issue:
- Volume 222(2019)
- Issue Display:
- Volume 222, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 222
- Issue:
- 2019
- Issue Sort Value:
- 2019-0222-2019-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-11
- Subjects:
- Liver targeted Nano-MitoPBN -- Reactive oxygen species -- Mitochondrial function -- Glycolysis -- Aerobic oxidation -- Type 2 diabetes
Biomedical materials -- Periodicals
Biocompatible Materials -- Periodicals
Biomatériaux -- Périodiques
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01429612 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01429612 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01429612 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.biomaterials.2019.119457 ↗
- Languages:
- English
- ISSNs:
- 0142-9612
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2087.715000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11715.xml