alexa Nanowired Antioxidant Compound H-290/51 Downregulates Ubiquitin And Heat Shock Proteins Expressions And Attenuates Exacerbation Of Spinal Cordpathology In Diabetic Rats Following Trauma
ISSN: 2157-7439

Journal of Nanomedicine & Nanotechnology
Open Access

Like us on:
OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations

700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Share This Page

Additional Info

Loading Please wait..

4th International Conference on Nanotek & Expo
December 01-03, 2014 DoubleTree by Hilton Hotel San Francisco Airport, USA

Aruna Sharma, Jose Vicente Lafuente, Dafin F Muresanu, Ranjana Patnaik, Z Ryan Tian, Per-Ove Sj?quist6 and Hari S Sharma
Posters: J Nanomed Nanotechnol
DOI: 10.4172/2157-7439.S1.018
Increased ubiquitin expression around injured axons or neurons in spinal cord injury (SCI) is associated with neuronal death whereas, accompanied increase in heat shock protein (HSP) 72 kD helps in cell survival. We examined ubiquitin and HSP immunoreactivity in SCI in healthy and in diabetic rats. A longitudinal incisionon the right dorsal horn of T10-11 segments (2 mm deep and 4 mm long) in the urethane-anesthetizedhealthy or diabetic rats (streptozotocine75 mg/kg. i.p. for 3 days) showed a marked increase in ubiquitin immunoreactivity in T9, T12 segments at 5h that extended further to T4 and L5 level after 8 h SCI. The magnitude and intensity of ubiquitin and HSP expression was exacerbated in diabetic rats after SCI. Posttreatment with a potent antioxidant compound H-290/51 (50 mg/kg, p.o 30 min after injury; Astra Zeneca, M?lndal, Sweden) markedly reduced the ubiquitin and HSP expression at 5 or 8 h after injury in healthy animals. However, diabetic group, TiO2 nanowired H-290/51 (50 mg/kg, p.o 30) is needed to reduce ubiquitin and HSP expressionsunder identical conditions. Taken together our observations are the first to demonstrate that (i) diabetic animals after injury results in overproduction of ubiquitin and HSP expression, (ii) this activation of ubiquitin and HSP is related to cord pathology, and (iii) nanowired H-290/51 is needed for neuroprotection in in diabetic animals after SCI.
Aruna Sharma MD in Indian Medicine from Banaras Hindu University, Varanasi, India 1976, she is Secretary for Research working in University Hospital in Anesthesiology & Intensive Care Medicine at the Uppsala University, Uppsala, Sweden. She has authored more than 150 research papers in reputed Neuroscience journals and her research interest includes CNS injury and repair under the influence of anesthetics, nanoparticles andco-morbidity factors e.g., diabetes or hypertension. She is associated with development of key Neuroscience journals and is acquisition Editor of American Journal of Neuroproetction and Neuroregenartion, and Journal of Nanoneuroscience, published from American Scientific Publishers, Los Angeles, CA, USA.
image PDF   |   image HTML
Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version