Anti-neuropathic pain activity of a cationic palladium (II) dithiocarbamate by suppressing the inflammatory mediators in paclitaxel-induced neuropathic pain model

Neuropathic pain is a chronic pain state that negatively impacts the quality of life. Currently, available therapies for the treatment of neuropathic pain often lack efficacy and tolerability. Therefore, the search for novel drugs is crucial to obtain treatments that effectively suppress neuropathic...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Naveed Muhammad
Ullah Rahim
Khan Adnan
Shal Bushra
Khan Ashraf Ullah
Khan Shahan Zeb
Rehman Zia Ur
Dokumentumtípus: Cikk
Megjelent: 2021
Sorozat:MOLECULAR BIOLOGY REPORTS 48
Tárgyszavak:
doi:10.1007/s11033-021-06754-7

mtmt:32478111
Online Access:http://publicatio.bibl.u-szeged.hu/22842
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520 3 |a Neuropathic pain is a chronic pain state that negatively impacts the quality of life. Currently, available therapies for the treatment of neuropathic pain often lack efficacy and tolerability. Therefore, the search for novel drugs is crucial to obtain treatments that effectively suppress neuropathic pain.The present study was undertaken to investigate the antinociceptive properties of (1,4-bis-(diphenylphosphino) butane) palladium (II) chloride monohydrate (Compound 1) in a paclitaxel (PTX)-induced neuropathic pain model.Initially, behavioral tests such as mechanical and cold allodynia as well as thermal and tail immersion hyperalgesia were performed to investigate the antinociceptive potential of Compound 1 (5 and 10 mg/kg, b.w). RT-PCR was performed to determine the effect of Compound 1 on the mRNA expression level of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and proinflammatory cytokines such as tumor necrosis factor-alpha (TNF)-α, interleukin (IL)-1β, and IL-6. In addition, antioxidant protein, nitric oxide (NO), and malondialdehyde (MDA) levels were also determined.The results demonstrated that once-daily dosing of Compound 1 significantly suppressed the PTX-induced behavioral pain responses dose-dependently. The mRNA gene expressions of iNOS, COX-2, and inflammatory cytokines were markedly reduced by Compound 1. Furthermore, it enhanced the level of antioxidant enzymes and lowered the level of MDA and NO production.These findings suggest that the antinociceptive potential of Compound 1 in the PTX-induced neuropathic pain model is via suppression of oxidative stress and inflammation. Thus, Compound 1 might be a potential candidate for the therapeutic management of PTX induced neuropathic pain. 
650 4 |a Klinikai orvostan 
700 0 1 |a Ullah Rahim  |e aut 
700 0 1 |a Khan Adnan  |e aut 
700 0 1 |a Shal Bushra  |e aut 
700 0 1 |a Khan Ashraf Ullah  |e aut 
700 0 1 |a Khan Shahan Zeb  |e aut 
700 0 1 |a Rehman Zia Ur  |e aut 
700 0 1 |a Khan Adnan  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/22842/1/NaveedMolBiolRep2021.pdf  |z Dokumentum-elérés