In vivo and in vitro protective effects of omeprazole against neuropathic pain

Sanjay K. Chanchal, Umesh B. Mahajan, Sumit Siddharth, Navyya Reddy, Sameer N. Goyal, Prakash H. Patil, Basavaraj P. Bommanahalli, Chanakya N. Kundu, Chandragouda R. Patil, Shreesh Ojha

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41 Citations (Scopus)


Apart from reducing the acid secretion, omeprazole inhibits activation of the nuclear factor-ΰ B, release of inflammatory cytokines, and chemotaxis of neutrophils. These mechanisms prompted us to evaluate antineuropathic effect of omeprazole in the chronic constriction injury (CCI)-induced rat model of neuropathic pain and LPS mediated ROS-induced U-87 cells. Omeprazole at 50 mg/kg/day/oral for 14 days significantly reduced the intensity of neuropathic pain estimated as paw withdrawal latency, withdrawal pressure threshold and restored the motor nerve conduction velocity in the constricted nerve, when compared with respective groups. The histological findings revealed the protective effect of omeprazole against the CCI-induced damage. Omeprazole significantly decreased the levels of tumor necrosis factor (TNF-α), interleukin-1β (IL-1β) and interleukin-6 (IL-6) as compared to their respective control groups. It also reduced the oxidative stress by up regulating the SOD, catalase activity and decreasing MDA content. Similarly, in-vitro study, LPS mediated ROS-induced U-87 cells, omeprazole reduced the oxidative stress as well as the release of TNF-α, IL-1β and IL-6. Altogether, these results suggest that, neuroprotective effect of omeprazole is mediated through preventing release of proinflammatory cytokines, augmenting endogenous anti-oxidant defense system, and maintain the structural integrity of sciatic nerve from the CCI-induced structural damage and inflammatory changes.

Original languageEnglish
Article number30007
JournalScientific reports
Publication statusPublished - Jul 20 2016

ASJC Scopus subject areas

  • General


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