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Histopathologic and immunohistochemical sequelae of bariatric embolization in a porcine model.

Publication ,  Journal Article
Paxton, BE; Alley, CL; Crow, JH; Burchette, J; Weiss, CR; Kraitchman, DL; Arepally, A; Kim, CY
Published in: J Vasc Interv Radiol
March 2014

PURPOSE: To evaluate the histopathologic sequelae of bariatric embolization on the gastric mucosa and to correlate with immunohistochemical evaluation of the gastric fundus, antrum, and duodenum. MATERIALS AND METHODS: This study was performed on 12 swine stomach and duodenum specimens after necropsy. Of the 12 swine, 6 had previously undergone bariatric embolization of the gastric fundus, and the 6 control swine had undergone a sham procedure with saline. Gross pathologic, histopathologic, and immunohistochemical examinations of the stomach and duodenum were performed. Specifically, mucosal integrity, fibrosis, ghrelin-expressing cells, and gastrin-expressing cells were assessed. RESULTS: Gross and histopathologic evaluation of treatment animals showed healing or healed mucosal ulcers in 50% of animals, with gastritis in 100% of treatment animals and in five of six control animals. The ghrelin-immunoreactive mean cell density was significantly lower in the gastric fundus in the treated animals compared with control animals (15.3 vs 22.0, P < .01) but similar in the gastric antrum (9.3 vs 14.3, P = .08) and duodenum (8.5 vs 8.6, P = .89). The gastrin-expressing cell density was significantly lower in the antrum of treated animals compared with control animals (82.2 vs 126.4, P = .03). A trend toward increased fibrosis was suggested in the gastric fundus of treated animals compared with controls (P = .07). CONCLUSIONS: Bariatric embolization resulted in a significant reduction in ghrelin-expressing cells in the gastric fundus without evidence of upregulation of ghrelin-expressing cells in the duodenum. Healing ulcerations in half of treated animals underscores the need for additional refinement of this procedure.

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Published In

J Vasc Interv Radiol

DOI

EISSN

1535-7732

Publication Date

March 2014

Volume

25

Issue

3

Start / End Page

455 / 461

Location

United States

Related Subject Headings

  • Tissue Distribution
  • Swine
  • Nuclear Medicine & Medical Imaging
  • Hemostatics
  • Ghrelin
  • Gastric Mucosa
  • Female
  • Embolization, Therapeutic
  • Animals
  • 3202 Clinical sciences
 

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Chicago
ICMJE
MLA
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Paxton, B. E., Alley, C. L., Crow, J. H., Burchette, J., Weiss, C. R., Kraitchman, D. L., … Kim, C. Y. (2014). Histopathologic and immunohistochemical sequelae of bariatric embolization in a porcine model. J Vasc Interv Radiol, 25(3), 455–461. https://doi.org/10.1016/j.jvir.2013.09.016
Paxton, Ben E., Christopher L. Alley, Jennifer H. Crow, James Burchette, Clifford R. Weiss, Dara L. Kraitchman, Aravind Arepally, and Charles Y. Kim. “Histopathologic and immunohistochemical sequelae of bariatric embolization in a porcine model.J Vasc Interv Radiol 25, no. 3 (March 2014): 455–61. https://doi.org/10.1016/j.jvir.2013.09.016.
Paxton BE, Alley CL, Crow JH, Burchette J, Weiss CR, Kraitchman DL, et al. Histopathologic and immunohistochemical sequelae of bariatric embolization in a porcine model. J Vasc Interv Radiol. 2014 Mar;25(3):455–61.
Paxton, Ben E., et al. “Histopathologic and immunohistochemical sequelae of bariatric embolization in a porcine model.J Vasc Interv Radiol, vol. 25, no. 3, Mar. 2014, pp. 455–61. Pubmed, doi:10.1016/j.jvir.2013.09.016.
Paxton BE, Alley CL, Crow JH, Burchette J, Weiss CR, Kraitchman DL, Arepally A, Kim CY. Histopathologic and immunohistochemical sequelae of bariatric embolization in a porcine model. J Vasc Interv Radiol. 2014 Mar;25(3):455–461.
Journal cover image

Published In

J Vasc Interv Radiol

DOI

EISSN

1535-7732

Publication Date

March 2014

Volume

25

Issue

3

Start / End Page

455 / 461

Location

United States

Related Subject Headings

  • Tissue Distribution
  • Swine
  • Nuclear Medicine & Medical Imaging
  • Hemostatics
  • Ghrelin
  • Gastric Mucosa
  • Female
  • Embolization, Therapeutic
  • Animals
  • 3202 Clinical sciences