Skip to main content
Log in

Beneficial Effect of Splanchnic Nerve Transection and Harmful Effect of Vagotomy on Acute Necrotizing Pancreatitis in the Dog

  • Original Article
  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

Background

The nervous system interacts dynamically with the immune system to modulate inflammation through humoral and neural pathways. However, the influence of visceral nerve (VN) on acute necrotizing pancreatitis (ANP) has drawn little attention.

Aim

To investigate the influence of VN on the pathophysiological process of ANP in dogs.

Methods

The dogs were divided into a sham operation (SO) group, ANP group, ANP + vagal nerve trunk transection (VNTT) group, and ANP + greater splanchnic nerve transection (GSNT) group. The VNTT and GSNT groups underwent VNTT and GSNT respectively immediately after ANP induction. The levels of serum pancreatic amylase (AMY), calcium, high-sensitivity C-reactive protein (HCRP), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-10 (IL-10) were monitored dynamically and the pathological examinations of the pancreas was performed at postoperative day 7.

Results

All serum parameters among the four groups showed no differences before the experiment (p > 0.05). At different postoperative times, the serum TNF-α, IL-1β, HCRP, and AMY were significantly increased, however, the serum calcium and IL-10 had dropped in the ANP group versus SO group (p < 0.05); an alike variation trend occurred between the VNTT group and ANP group (p < 0.05); an opposite variation trend occurred between the GSNT group and the ANP group (p < 0.05). The pancreas pathological scoring of VNTT group was highest in the four groups (p < 0.05) and GSNT group was lower versus ANP group (p < 0.05).

Conclusions

The GSNT has been shown to alleviate development of ANP, however, VNTT may exacerbate the ANP.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Rosas-Ballina M, Tracey KJ. Cholinergic control of inflammation. J Int Med. 2009;265:663–679.

    Article  CAS  Google Scholar 

  2. Tracey KJ. The inflammatory reflex. Nature. 2002;420:853–859.

    Article  CAS  PubMed  Google Scholar 

  3. Pavlov VA, Parrish WR, Rosas-Ballina M, et al. Brain acetylcholinesterase activity controls systemic cytokine levels through the cholinergic anti-inflammatory pathway. Brain Behav Immun. 2009;23:41–45.

    Article  CAS  PubMed  Google Scholar 

  4. Kalsner S. Autoregulation of neurotransmitter release at autonomic nerve terminals: a questionable theory. J Auton Pharmacol. 2000;20:271–279.

    Article  CAS  PubMed  Google Scholar 

  5. Grogan EL, Morris JA Jr, Norris PR, et al. Reduced heart rate volatility: an early predictor of death in trauma patients. Ann Surg. 2004;240:547–556.

    Article  PubMed Central  PubMed  Google Scholar 

  6. Wu C, Li Z. Mutt main pancreatic duct anatomy and pancreatitis model making. World Chin J Digestol. 1999;7:62–63.

    Google Scholar 

  7. Rongione AR, Kusske AM, Kan K, et al. Interleukin 10 reduces the severity of acute pancreatitis in rats. Gastroenterology. 1997;112:960–967.

    Article  CAS  PubMed  Google Scholar 

  8. Steinman L. Elaborate interactions between immune and nervous systems. Nat Immunol. 2004;5:575–581.

    Article  CAS  PubMed  Google Scholar 

  9. Borovikova LV, Ivanova S, Zhang M, et al. Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin. Nature. 2000;405:458–462.

    Article  CAS  PubMed  Google Scholar 

  10. Miksa M, Wu R, Zhou M, et al. Sympathetic excitotoxicity in sepsis: pro-inflammatory priming of macrophages by norepinephrine. Front Biosci. 2005;10:2217–2229.

    Article  CAS  PubMed  Google Scholar 

  11. Li J, Xiong J, Chen D, et al. Effect of vagotomy on acute pancreatitis in rats. J Tongji Med Univ. 2000;20:235–238.

    Article  CAS  PubMed  Google Scholar 

  12. Szklarczyk J, Jaworek J, Czech U, et al. Bilateral vagotomy attenuates the severity of secretagogue-induced acute pancreatitis in the rat. Adv Med Sci. 2014;39:1–6.

    Google Scholar 

  13. Carroll JK, Herrick B, Gipson T, et al. Acute pancreatitis: diagnosis, prognosis, and treatment. Am Fam Physician. 2007;75:1513–1520.

    PubMed  Google Scholar 

  14. Guice KS, Oldham KT, Remick DG, et al. Anti-tumor necrosis factor antibody augments edema formation in caerulein-induced acute pancreatitis. J Surg Res. 1991;51:495–499.

    Article  CAS  PubMed  Google Scholar 

  15. Elfar M, Gaber LW, Sabek O, et al. The inflammatory cascade in acute pancreatitis: relevance to clinical disease. Surg Clin North Am, 2007;87:1325–1340, vii.

  16. Zhang XP, Zhang J, Ma ML, et al. Pathological changes at early stage of multiple organ injury in a rat model of severe acute pancreatitis. Hepatobiliary Pancreat Dis Int. 2010;9:83–87.

    CAS  PubMed  Google Scholar 

  17. Xu P, Zhou XJ, Chen LQ, et al. Pioglitazone attenuates the severity of sodium taurocholate-induced severe acute pancreatitis. World J Gastroenterol. 2007;13:1983–1988.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  18. The FO, Boeckxstaens GE, Snoek SA, et al. Activation of the cholinergic anti-inflammatory pathway ameliorates postoperative ileus in mice. Gastroenterology. 2007;133:1219–1228.

    Article  CAS  PubMed  Google Scholar 

  19. Demirag A, Pastor CM, Morel P, et al. Epidural anaesthesia restores pancreatic microcirculation and decreases the severity of acute pancreatitis. World J Gastroenterol. 2006;12:915–920.

    PubMed Central  PubMed  Google Scholar 

  20. Bernhardt A, Kortgen A, Niesel HCh, et al. Using epidural anesthesia in patients with acute pancreatitis–prospective study of 121 patients. Anaesthesiol Reanim. 2002;27:16–22.

    CAS  PubMed  Google Scholar 

  21. Sun Jun–Jun, Chu Zhi-Jie, Liu Wei-Feng, et al. Perirenal space blocking restores gastrointestinal function in patients with severe acute pancreatitis. World J Gastroenterol. 2013;19:8752–8757.

    Article  PubMed Central  PubMed  Google Scholar 

  22. Fritz S, Hackert T, Hartwig W, et al. Bacterial translocation and infected pancreatic necrosis in acute necrotizing pancreatitis derives from small bowel rather than from colon. Am J Surg. 2010;200:111–117.

    Article  PubMed  Google Scholar 

  23. Sielenkamper AW, Eicker K, Van Aken H. Thoracic epidural anesthesia increases mucosal perfusion in ileum of rats. Anesthesiology. 2000;93:844–851.

    Article  CAS  PubMed  Google Scholar 

  24. Sielenkamper AW, Eicker K, Van Aken H. Thoracic epidural anesthesia increases mucosal perfusion in ileum of rats. Anesthesiology. 2000;93:844–851.

    Article  CAS  PubMed  Google Scholar 

  25. Kusske AM, Rongione AJ, Reber HA. Cytokines and acute pancreatitis. Gastroenterology. 1996;110:639–642.

    Article  CAS  PubMed  Google Scholar 

  26. Leindler L, Morschl E, László F, et al. Importance of cytokines, nitric oxide, and apoptosis in the pathological process of necrotizing pancreatitis in rats. Pancreas. 2004;29:157–161.

    Article  CAS  PubMed  Google Scholar 

  27. Gerard C, Bruyns C, Marchant A, et al. Interleukin-10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia. J Exp Med. 1993;177:547–550.

    Article  CAS  PubMed  Google Scholar 

  28. Van Laethem JL, Eskinazi R, Louis H, et al. Multisystemic production of interleukin 10 limits the severity of acute pancreatitis in mice. Gut. 1998;43:408–413.

    Article  PubMed Central  PubMed  Google Scholar 

  29. Triester SL, Kowdley KV. Prognostic factors in acute pancreatitis. J Clin Gastroenterol. 2002;34:167–176.

    Article  PubMed  Google Scholar 

  30. Pezzilli R, Melzi D’eril GV, Morselli-labate AM, et al. Serum amyloid A, procalcitonin, and C-reactive protein in early assessment of acute pancreatitis. Dig Dis Sci. 2000;45:1072–1078.

    Article  CAS  PubMed  Google Scholar 

  31. Zhen G, Sun J, Liu W, et al. A1-acid glycoprotein and allergic C-reactive protein in the early acute pancreatitis severity evaluation of the dynamic monitoring of significance. Chin J Exp Surg. 2010;27:23–25.

    Google Scholar 

  32. Kylanpaa-Back ML, Takala A, Kemppainen E, et al. Procalcitonin strip teat in the early detection of severe acute pancreatitis. Br J Surg. 2001;88:222–227.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The authors gratefully acknowledge the assistance of Dr. Jianqiang Mi in histopathological experiments. This study was funded by Cultivating Fund of Henan University of Science and Technology.

Conflict of interest

There are no potential conflicts of interest to disclose for all authors.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jun-Jun Sun.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sun, JJ., Chu, ZJ., Zhang, YM. et al. Beneficial Effect of Splanchnic Nerve Transection and Harmful Effect of Vagotomy on Acute Necrotizing Pancreatitis in the Dog. Dig Dis Sci 60, 118–126 (2015). https://doi.org/10.1007/s10620-014-3315-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10620-014-3315-z

Keywords

Navigation