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Hydrogen sulfide as a novel mediator for pancreatic pain in rodents
  1. Sachiyo Nishimura
  1. Kinki University, Japan
    1. Osamu Fukushima
    1. Kinki University, Japan
      1. Hiroyasu Ishikura
      1. Kyoto Medical Center, Japan
        1. Tomoko Takahashi
        1. Kinki University, Japan
          1. Maho Matsunami
          1. Kinki University, Japan
            1. Toshifumi Tsujiuchi
            1. Kinki University, Japan
              1. Fumiko Sekiguchi
              1. Kinki University, Japan
                1. Mitsuhide Naruse
                1. Kyoto Medical Center, Japan
                  1. Yoshihisa Kamanaka
                  1. Ono Pharmaceutical Co. Ltd., Japan
                    1. Atsufumi Kawabata (kawabata{at}
                    1. Kinki University School of Pharmacy, Japan


                      Objective: Hydrogen sulfide (H2S) is formed from L-cysteine by multiple enzymes including cystathionine-γ-synthase (CSE) in mammals, and plays various roles in health and disease. Recently, we identified a pro-nociceptive role of H2S in the processing of somatic pain. Here, we examined the involvement of H2S in pancreatic pain.

                      Methods: Anesthetized rats or mice received an injection of NaHS, a donor for H2S, or capsaicin into the pancreatic duct, and the expression of spinal Fos protein was detected by immunohistochemistry. Pancreatitis was created by 6 hourly doses of caerulein in unanesthetized mice, and pancreatitis-related allodynia/hyperalgesia was evaluated using von Frey hairs. CSE activity and protein levels in pancreatic tissues were measured using the colorimetric method and Western blotting, respectively.

                      Results: Either NaHS or capsaicin induced the expression of Fos protein in the superficial layers of the T8 and T9 spinal dorsal horn of rats or mice. The induction of Fos by NaHS but not capsaicin was abolished by mibefradil, a T-type Ca2+ channel blocker. In conscious mice, repeated doses of caerulein produced pancreatitis accompanied by abdominal allodynia/hyperalgesia. Pretreatment with an inhibitor of CSE prevented the allodynia/hyperalgesia, but not the pancreatitis. A single dose of mibefradil reversed the established pancreatitis-related allodynia/hyperalgesia. Either the activity or protein expression of pancreatic CSE increased after the development of caerulein-induced pancreatitis in mice.

                      Conclusions: Our data suggest that pancreatic NaHS/H2S most probably targets T-type Ca2+ channels, leading to nociception, and that endogenous H2S produced by CSE and possibly T-type Ca2+ channels are involved in pancreatitis-related pain.

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