Publications

Latest publication 12/16/2014

Nociceptive spinal cord neurons of laminae I-III exhibit oxidative stress damage

Spinal cord neurons located in laminae I-III respond to nociceptive stimuli and participate in the transmission of painful information to the...

Array
(
    [id_prestablog_news] => 667
    [id_shop] => 1
    [date] => 2014-12-16 00:00:00
    [date_modification] => 2024-02-09 14:15:11
    [langues] => ["1","2"]
    [actif] => 1
    [slide] => 0
    [url_redirect] => 
    [average_rating] => 
    [number_rating] => 
    [author_id] => 1
    [featured] => 0
    [prim_key] => 1303
    [id_lang] => 1
    [title] => Nociceptive spinal cord neurons of laminae I-III exhibit oxidative stress damage
    [paragraph] => Nociceptive spinal cord neurons of laminae I-III exhibit oxidative stress damage during diabetic neuropathy which is prevented by early antioxidant treatment with epigallocatechin-gallate (EGCG)
    [content] => 

Authors
Raposo D, Morgado C, Pereira-Terra P, Tavares I


Lab
Faculty of Medicine, University of Porto, Portugal; IBMC, University of Porto, Portugal.

Journal
Brain Res Bull.

Abstract
Spinal cord neurons located in laminae I-III respond to nociceptive stimuli and participate in the transmission of painful information to the brain. In the present study we evaluated if nociceptive laminae I-III neurons are affected by oxidative stress damage in a model of diabetic neuropathic pain (DNP), the streptozotocin-induced diabetic rat (STZ rat). Additionally, we evaluated the effects of a preventive antioxidant treatment with epigallocatechin-gallate (EGCG) in nociceptive neuronal activation and behavioural signs of DNP. Three days after diabetes induction, a treatment protocol of STZ rats with an aqueous solution of EGCG in the drinking water was initiated. Ten weeks after the onset of treatment, the spinal cords were immunoreacted against validated markers of oxidative stress damage (8-hydroxy-2-deoxyguanosine; 8-OHdG) and of nociceptive neuronal activation (Fos). Mechanical hypersensitivity was assessed before and after EGCG treatment. Untreated STZ rats presented increased levels of 8-OHdG immunoreaction, higher numbers of Fos-immunoreacted neurons and high levels of co-localization of 8-OHdG and Fos in laminae I-III. Treatment with EGCG normalized the increase of the above mentioned parameters and ameliorated mechanical hypersensitivity. The present study shows that nociceptive neurons in spinal cord laminae I-III exhibit oxidative stress damage during diabetic neuropathy, which probably affects ascending pain transmission during DNP. The neurobiological mechanisms and translational perspectives of the beneficial effects of a preventive and sustained EGCG treatment in DNP need to be evaluated in the future.

BIOSEB Instruments Used
Electronic Von Frey 4 (BIO-EVF4),Electronic Von Frey 5 with embedded camera (BIO-EVF5)

[meta_description] => [meta_keywords] => http://www.ncbi.nlm.nih.gov/pubmed/25522867 [meta_title] => [link_rewrite] => nociceptive-spinal-cord-neurons-of-laminae-i-iii-exhibit-oxidative-stress-damage-during-diabetic-neuropathy-which-is-prevented-by-early-antioxidant-treatment-with-epigallocatechin-gallate--egcg- [actif_langue] => 1 [read] => 1108 [count_comments] => 0 [id] => 667 [categories] => Array ( [36] => Array ( [id_prestablog_categorie] => 36 [title] => Mechanical allodynia & Hyperlagesia [link_rewrite] => Mechanical-allodynia-hyperlagesia ) [23] => Array ( [id_prestablog_categorie] => 23 [title] => Metabolism [link_rewrite] => Metabolism ) [29] => Array ( [id_prestablog_categorie] => 29 [title] => Neuropathic pain [link_rewrite] => Neuropathic-pain ) [86] => Array ( [id_prestablog_categorie] => 86 [title] => Oxidative stress [link_rewrite] => Oxidative-stress ) [10] => Array ( [id_prestablog_categorie] => 10 [title] => Pain [link_rewrite] => Pain ) [2] => Array ( [id_prestablog_categorie] => 2 [title] => Publications [link_rewrite] => publications ) ) [authors] => [paragraph_crop] => Nociceptive spinal cord neurons of laminae I-III exhibit oxidative stress damage during [...] [link_for_unique] => 1 [products_liaison] => Array ( [1859] => Array ( [name] => Electronic Von Frey - Wireless [description_short] =>

A quick solution to determine the mechanical sensitivity threshold in rodents (mice and rats). Now wireless, to be free from annoying cables!

This precise and easy-to-use electronic instrument is a must-have reference for your research in analgesia, nociception, neuro-pathologies and post-operative pain.

Instrument for ratsInstrument for mice

[thumb] => [img_empty] => /var/www/vhosts/de3310.ispfr.net/bioseb2024/modules/prestablog/views/img/product_link_white.jpg [image_presente] => 1 [link] => https://bioseb.com/en/pain-mechanical-allodynia-hyperalgesia/1859-electronic-von-frey-4.html ) [1860] => Array ( [name] => Electronic Von Frey 5 with embedded camera [description_short] =>

As an electronic version of the classical Von Frey Filaments esthesiometer (or aesthesiometer), the latest evolution of Bioseb's Electronic Von Frey instrument for determining the mechanical sensitivity threshold in rodents (rats and mice) is a must-have instrument for your reseach on hyperalgesia and allodynia. By measuring and recording the force at which the animal exhibits a paw withdrawal reflex, pathologies related to sensory response and hyper- or hypo-aesthesia can be studied.

The EVF5 includes an embedded camera inside the stimulator handle and a new, dedicated software revolutionizing the experimental process.

Instrument for ratsInstrument for mice

[thumb] => [img_empty] => /var/www/vhosts/de3310.ispfr.net/bioseb2024/modules/prestablog/views/img/product_link_white.jpg [image_presente] => 1 [link] => https://bioseb.com/en/pain-mechanical-allodynia-hyperalgesia/1860-electronic-von-frey-5-with-embedded-camera.html ) ) ) 1
Read more

Filters

Applications

Dates

<< 1 ... 90 91 92 93 94 >>