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American journal of veterinary research2017; 78(8); 977-989; doi: 10.2460/ajvr.78.8.977

Effect of lidocaine on inflammation in equine jejunum subjected to manipulation only and remote to intestinal segments subjected to ischemia.

Abstract: OBJECTIVE To examine effects of continuous rate infusion of lidocaine on transmural neutrophil infiltration in equine intestine subjected to manipulation only and remote to ischemic intestine. ANIMALS 14 healthy horses. PROCEDURES Ventral midline celiotomy was performed (time 0). Mild ischemia was induced in segments of jejunum and large colon. A 1-m segment of jejunum was manipulated by massaging the jejunal wall 10 times. Horses received lidocaine (n = 7) or saline (0.9% NaCl) solution (7) throughout anesthesia. Biopsy specimens were collected and used to assess tissue injury, neutrophil influx, cyclooxygenase expression, and hypoxia-inducible factor 1α (HIF-1α) expression at 0, 1, and 4 hours after manipulation and ischemia. Transepithelial resistance (TER) and mannitol flux were measured by use of Ussing chambers. RESULTS Lidocaine did not consistently decrease neutrophil infiltration in ischemic, manipulated, or control tissues at 4 hours. Lidocaine significantly reduced circular muscle and overall scores for cyclooxygenase-2 expression in manipulated tissues. Manipulated tissues had significantly less HIF-1α expression at 4 hours than did control tissues. Mucosa from manipulated and control segments obtained at 4 hours had lower TER and greater mannitol flux than did control tissues at 0 hours. Lidocaine did not significantly decrease calprotectin expression. Severity of neutrophil infiltration was similar in control, ischemic, and manipulated tissues at 4 hours. CONCLUSIONS AND CLINICAL RELEVANCE Manipulated jejunum did not have a significantly greater increase in neutrophil infiltration, compared with 4-hour control (nonmanipulated) jejunum remote to sites of manipulation, ischemia, and reperfusion. Lidocaine did not consistently reduce neutrophil infiltration in jejunum.
Publication Date: 2017-07-25 PubMed ID: 28738006DOI: 10.2460/ajvr.78.8.977Google Scholar: Lookup
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  • Journal Article
  • Randomized Controlled Trial

Summary

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This research investigated how lidocaine impacts neutrophil infiltration (a sign of inflammation) in a horse’s manipulated intestine and parts of the intestine remote to ischemic areas. The study found that lidocaine did not consistently lower neutrophil infiltration, suggesting its limited impact on inflammation in this context.

Experimental Procedure

  • Animals used in this study were 14 healthy horses. All the horses underwent a surgical procedure called ventral midline celiotomy.
  • Post-surgery, mild ischemia, a condition of reduced blood flow, was induced in portions of the jejunum and the large colon.
  • In a part of the jejunum, manipulation was done by massaging the jejunal wall ten times. During the course of anesthesia, the horses either received lidocaine or a saline solution.
  • By getting biopsy specimens at 0, 1, and 4 hours after manipulation and ischemia, researchers could assess tissue injury, neutrophil influx, expression of cyclooxygenase (an enzyme involved in inflammation), and the expression of hypoxia-inducible factor 1α (a transcription factor that responds to reduced oxygen in the cell).
  • They also measured transepithelial resistance (TER) and mannitol flux with the help of Ussing chambers. TER is a measure of the intestine’s epithelial barrier function, and mannitol flux measures the permeability of the barrier.

Main Results

  • Lidocaine did not consistently decrease neutrophil infiltration in ischemic, manipulated, or control tissues.
  • Lidocaine meaningfully reduced circular muscle and overall scores for cyclooxygenase-2 expression in manipulated tissues. Cyclooxygenase-2 is an enzyme that plays a critical role in inflammation, and so this finding suggests lidocaine might have some anti-inflammatory effects.
  • Manipulated tissues had significantly less hypoxia-inducible factor 1α expression at 4 hours than control tissues.
  • At 4 hours, the mucosa from manipulated and control segments showed lower TER and greater mannitol flux than the control tissues at 0 hours. This indicates that manipulation disturbs the normal functioning of the intestinal barrier.
  • Lidocaine did not significantly decrease calprotectin expression. Calprotectin is a protein found in neutrophil cytosol and is often used to assess inflammation in the body.
  • The degree of neutrophil infiltration was similar across control, ischemic, and manipulated tissues after 4 hours.

Conclusions and Clinical Relevance

  • The study concluded that manipulated jejunum did not have a significantly larger increase in neutrophil infiltration compared with the control (nonmanipulated) jejunum.
  • Furthermore, lidocaine did not consistently reduce neutrophil infiltration in the jejunum, implying that it may not be effective at reducing inflammation in these tissues.

Cite This Article

APA
Bauck AG, Grosche A, Morton AJ, Graham AS, Vickroy TW, Freeman DE. (2017). Effect of lidocaine on inflammation in equine jejunum subjected to manipulation only and remote to intestinal segments subjected to ischemia. Am J Vet Res, 78(8), 977-989. https://doi.org/10.2460/ajvr.78.8.977

Publication

ISSN: 1943-5681
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 78
Issue: 8
Pages: 977-989

Researcher Affiliations

Bauck, Anje G
    Grosche, Astrid
      Morton, Alison J
        Graham, A Sarah
          Vickroy, Thomas W
            Freeman, David E

              MeSH Terms

              • Animals
              • Cyclooxygenase 2 / metabolism
              • Horse Diseases / drug therapy
              • Horse Diseases / pathology
              • Horses
              • Inflammation / drug therapy
              • Inflammation / metabolism
              • Inflammation / veterinary
              • Intestinal Mucosa / metabolism
              • Ischemia / metabolism
              • Jejunal Diseases / drug therapy
              • Jejunal Diseases / veterinary
              • Jejunum / blood supply
              • Lidocaine / pharmacology
              • Lidocaine / therapeutic use
              • Neutrophils / metabolism

              Citations

              This article has been cited 7 times.
              1. Bardell D, Rocchigiani G, Ressel L, Milner P. Histological Evaluation of Resected Tissue as a Predictor of Survival in Horses with Strangulating Small Intestinal Disease. Animals (Basel) 2023 Aug 26;13(17).
                doi: 10.3390/ani13172715pubmed: 37684979google scholar: lookup
              2. Verhaar N, de Buhr N, von Köckritz-Blickwede M, Dümmer K, Hewicker-Trautwein M, Pfarrer C, Dengler F, Kästner S. Hypoxia signaling in the equine small intestine: Expression and distribution of hypoxia inducible factors during experimental ischemia. Front Vet Sci 2023;10:1110019.
                doi: 10.3389/fvets.2023.1110019pubmed: 36908508google scholar: lookup
              3. Dengler F, Sternberg F, Grages M, Kästner SB, Verhaar N. Adaptive mechanisms in no flow vs. low flow ischemia in equine jejunum epithelium: Different paths to the same destination. Front Vet Sci 2022;9:947482.
                doi: 10.3389/fvets.2022.947482pubmed: 36157182google scholar: lookup
              4. Grages AM, Verhaar N, Pfarrer C, Breves G, Burmester M, Neudeck S, Kästner S. Low Flow versus No Flow: Ischaemia Reperfusion Injury Following Different Experimental Models in the Equine Small Intestine. Animals (Basel) 2022 Aug 22;12(16).
                doi: 10.3390/ani12162158pubmed: 36009747google scholar: lookup
              5. Verhaar N, de Buhr N, von Köckritz-Blickwede M, Hewicker-Trautwein M, Pfarrer C, Mazzuoli-Weber G, Schulte H, Kästner S. Ischaemic postconditioning reduces apoptosis in experimental jejunal ischaemia in horses. BMC Vet Res 2021 Apr 26;17(1):175.
                doi: 10.1186/s12917-021-02877-ypubmed: 33902575google scholar: lookup
              6. Wu J, Chen Q, He Z, Yang B, Dai Z, Qiu F. Immunomodulatory Effects of Lidocaine: Mechanisms of Actions and Therapeutic Applications. Pharmaceuticals (Basel) 2026 Jan 12;19(1).
                doi: 10.3390/ph19010134pubmed: 41599732google scholar: lookup
              7. Stewart AS, Kopper JJ, McKinney-Aguirre C, Veerasamy B, Sahoo DK, Freund JM, Gonzalez LM. Assessment of equine intestinal epithelial junctional complexes and barrier permeability using a monolayer culture system. Front Vet Sci 2024;11:1455262.
                doi: 10.3389/fvets.2024.1455262pubmed: 39502947google scholar: lookup