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      Attenuation of Unevoked Mechanical and Cold Pain Hypersensitivities Associated With Experimental Neuropathy in Mice by Angiotensin II Type-2 Receptor Antagonism

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      , PhD, , PhD
      Anesthesia and analgesia

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          Abstract

          Recent findings from a phase II clinical trial showed analgesic effects of an angiotensin II type-2 receptor (AT2R) antagonist in postherpetic neuralgia patients. This study aimed to investigate whether AT2R antagonism could provide effective analgesia in voluntary measures of unevoked/ongoing pain-like behaviors in mice with experimental neuropathy. Mice were subjected to spared nerve injury to induce neuropathy and tested in 2 operant behavioral tests to measure ongoing mechanical and cold pain hypersensitivities. Systemic administration of an AT2R antagonist provided effective analgesia in these behavioral measures of mechanical and cold pain in spared nerve injury mice, suggesting its effectiveness in neuropathic pain.

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          Author and article information

          Journal
          1310650
          530
          Anesth Analg
          Anesth. Analg.
          Anesthesia and analgesia
          0003-2999
          1526-7598
          17 July 2019
          June 2019
          01 June 2020
          : 128
          : 6
          : e84-e87
          Affiliations
          Department of Anesthesiology and Washington University Pain Center, Washington University School of Medicine in St. Louis, St Louis, Missouri.
          Author notes

          Reprints will not be available from the authors.

          Address correspondence to Andrew J. Shepherd, PhD, Department of Anesthesiology and Washington University Pain Center, Washington University School of Medicine in St Louis, St Louis, MO 63110. to a.shepherd@ 123456wustl.edu ; and Durga P. Mohapatra, PhD, Department of Anesthesiology and Washington University Pain Center, Washington University School of Medicine in St Louis, St Louis, MO 63110. to d.p.mohapatra@ 123456wustl.edu .
          Article
          PMC6652216 PMC6652216 6652216 nihpa1035463
          10.1213/ANE.0000000000003857
          6652216
          31094778
          8e7a4a38-4c2e-4014-a379-eee4cd326f9f
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