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  • Sharma, ArunaUppsala universitet,Anestesiologi och intensivvård,Uppsala Univ, Int Expt CNS Injury & Repair, Univ Hosp, Frodingsgatan 12,Bldg 28, SE-75421 Uppsala, Sweden.;Univ Basque Country UPV EHU, Dept Neurosci, LaNCE, Leioa, Bizkaia, Spain. (author)

Cold Environment Exacerbates Brain Pathology and Oxidative Stress Following Traumatic Brain Injuries : Potential Therapeutic Effects of Nanowired Antioxidant Compound H-290/51

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2017-08-30
  • Humana Press,2018
  • printrdacarrier

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  • LIBRIS-ID:oai:DiVA.org:uu-346900
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-346900URI
  • https://doi.org/10.1007/s12035-017-0740-yDOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:137624805URI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • The possibility that traumatic brain injury (TBI) occurring in a cold environment exacerbates brain pathology and oxidative stress was examined in our rat model. TBI was inflicted by making a longitudinal incision into the right parietal cerebral cortex (2 mm deep and 4 mm long) in cold-acclimatized rats (5 degrees C for 3 h daily for 5 weeks) or animals at room temperature under Equithesin anesthesia. TBI in cold-exposed rats exhibited pronounced increase in brain lucigenin (LCG), luminol (LUM), and malondialdehyde (MDA) and marked pronounced decrease in glutathione (GTH) as compared to identical TBI at room temperature. The magnitude and intensity of BBB breakdown to radioiodine and Evans blue albumin, edema formation, and neuronal injuries were also exacerbated in cold-exposed rats after injury as compared to room temperature. Nanowired delivery of H-290/51 (50 mg/kg) 6 and 8 h after injury in cold-exposed group significantly thwarted brain pathology and oxidative stress whereas normal delivery of H-290/51 was neuroprotective after TBI at room temperature only. These observations are the first to demonstrate that (i) cold aggravates the pathophysiology of TBI possibly due to an enhanced production of oxidative stress, (ii) and in such conditions, nanodelivery of antioxidant compound has superior neuroprotective effects, not reported earlier.

Subject headings and genre

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  • Muresanu, Dafin F.RoNeuro Inst Neurol Res & Diagnost, 37 Mircea Eliade St, Cluj Napoca 400364, Romania.;Univ Med & Pharm, Dept Clin Neurosci, Cluj Napoca, Romania. (author)
  • Vicente Lafuente, JoseUniv Basque Country UPV EHU, Dept Neurosci, LaNCE, Leioa, Bizkaia, Spain.;BioCruces Hlth Res Inst, Nanoneurosurg Grp, Baracaldo 48903, Bizkaia, Spain.;Univ Autonoma Chile, Fac Hlth Sci, Santiago, Chile. (author)
  • Sjöquist, Per-OveKarolinska Univ Hosp, Karolinska Inst, Div Cardiol, Dept Med, Stockholm, Sweden. (author)
  • Patnaik, RanjanaBanaras Hindu Univ, Sch Biomed Engn, Dept Biomat, Indian Inst Technol, Varanasi, Uttar Pradesh, India. (author)
  • Tian, Z. RyanUniv Arkansas, Dept Chem & Biochem, Fayetteville, AR 72701 USA. (author)
  • Ozkizilcik, AsyaUniv Arkansas, Dept Biomed Engn, Fayetteville, AR 72701 USA. (author)
  • Sharma, Hari S.Uppsala universitet,Anestesiologi och intensivvård,Uppsala Univ, Int Expt CNS Injury & Repair, Univ Hosp, Frodingsgatan 12,Bldg 28, SE-75421 Uppsala, Sweden.;Univ Basque Country UPV EHU, Dept Neurosci, LaNCE, Leioa, Bizkaia, Spain.(Swepub:uu)hssharma (author)
  • Uppsala universitetAnestesiologi och intensivvård (creator_code:org_t)

Related titles

  • In:Molecular Neurobiology: Humana Press55:1, s. 276-2850893-76481559-1182

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