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Smooth muscle actin as a novel serologic marker of severe intestinal damage in rat intestinal ischemia-reperfusion and human necrotising enterocolitis

Smooth muscle actin as a novel serologic marker of severe intestinal damage in rat intestinal ischemia-reperfusion and human necrotising enterocolitis
Smooth muscle actin as a novel serologic marker of severe intestinal damage in rat intestinal ischemia-reperfusion and human necrotising enterocolitis
BACKGROUND: Despite emergence of markers of intestinal mucosal damage such as intestinal fatty-acid binding protein (i-FABP), there are no specific markers of damage extending into the muscle layers. We hypothesized that smooth muscle actin (SMA) released from the intestinal muscularis would be detectable in plasma after severe intestinal injury.

MATERIALS AND METHODS: Serial blood samples were collected from rats (n = 10) undergoing intestinal ischemia-reperfusion injury (IRI) and controls (n = 5). Additionally, admission and/or preoperative plasma samples were collected from twelve neonates with necrotizing enterocolitis (NEC), and five age- and weight-matched controls. Plasma ileal fatty-acid binding protein (rat) or i-FABP (human) were measured by enzyme-linked immunosorbent assay, and plasma SMA was detected by western blotting.

RESULTS: Plasma ileal fatty-acid binding protein was low in both the control group and IRI at baseline, but became rapidly elevated in the IRI group even during ischemia. SMA was detected in reperfusion plasma samples of all IRI rats, but in none of the control samples. Plasma i-FABP was higher in infants with NEC than age- and weight-matched controls. Although i-FABP was higher in infants with severe surgical disease compared with focal disease, there was no difference between the operative and nonoperative groups. SMA was detected in the plasma of all four neonates with severe surgical NEC, but not in those with focal disease or those who were successfully conservatively managed.

CONCLUSIONS: SMA is detectable in plasma after severe intestinal injury and maybe a clinically useful maker of intestinal muscle damage.
smooth muscle actin, serum marker, diagnostic marker, intestinal ischemia, transmural intestinal necrosis, necrotizing enterocolitis
0022-4804
323-330
Evennett, Nicholas
f82e4f77-0c85-414b-9ac0-6132e45b665a
Cerigioni, Elisabetta
6ca5e7cf-0d4a-402b-a4fa-22b5f4418337
Hall, Nigel J.
6919e8af-3890-42c1-98a7-c110791957cf
Pierro, Agostino
74bd6b37-4305-47fd-847d-c19a08718997
Eaton, Simon
e14103c2-c06a-45e6-87fe-2358a3371283
Evennett, Nicholas
f82e4f77-0c85-414b-9ac0-6132e45b665a
Cerigioni, Elisabetta
6ca5e7cf-0d4a-402b-a4fa-22b5f4418337
Hall, Nigel J.
6919e8af-3890-42c1-98a7-c110791957cf
Pierro, Agostino
74bd6b37-4305-47fd-847d-c19a08718997
Eaton, Simon
e14103c2-c06a-45e6-87fe-2358a3371283

Evennett, Nicholas, Cerigioni, Elisabetta, Hall, Nigel J., Pierro, Agostino and Eaton, Simon (2014) Smooth muscle actin as a novel serologic marker of severe intestinal damage in rat intestinal ischemia-reperfusion and human necrotising enterocolitis. The Journal of Surgical Research, 191 (2), 323-330. (doi:10.1016/j.jss.2014.04.020). (PMID:24909869)

Record type: Article

Abstract

BACKGROUND: Despite emergence of markers of intestinal mucosal damage such as intestinal fatty-acid binding protein (i-FABP), there are no specific markers of damage extending into the muscle layers. We hypothesized that smooth muscle actin (SMA) released from the intestinal muscularis would be detectable in plasma after severe intestinal injury.

MATERIALS AND METHODS: Serial blood samples were collected from rats (n = 10) undergoing intestinal ischemia-reperfusion injury (IRI) and controls (n = 5). Additionally, admission and/or preoperative plasma samples were collected from twelve neonates with necrotizing enterocolitis (NEC), and five age- and weight-matched controls. Plasma ileal fatty-acid binding protein (rat) or i-FABP (human) were measured by enzyme-linked immunosorbent assay, and plasma SMA was detected by western blotting.

RESULTS: Plasma ileal fatty-acid binding protein was low in both the control group and IRI at baseline, but became rapidly elevated in the IRI group even during ischemia. SMA was detected in reperfusion plasma samples of all IRI rats, but in none of the control samples. Plasma i-FABP was higher in infants with NEC than age- and weight-matched controls. Although i-FABP was higher in infants with severe surgical disease compared with focal disease, there was no difference between the operative and nonoperative groups. SMA was detected in the plasma of all four neonates with severe surgical NEC, but not in those with focal disease or those who were successfully conservatively managed.

CONCLUSIONS: SMA is detectable in plasma after severe intestinal injury and maybe a clinically useful maker of intestinal muscle damage.

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More information

Accepted/In Press date: 9 April 2014
e-pub ahead of print date: 14 April 2014
Published date: October 2014
Keywords: smooth muscle actin, serum marker, diagnostic marker, intestinal ischemia, transmural intestinal necrosis, necrotizing enterocolitis
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 375549
URI: http://eprints.soton.ac.uk/id/eprint/375549
ISSN: 0022-4804
PURE UUID: 1ef00a40-a1d2-47e4-94e7-fc6ded0adae7
ORCID for Nigel J. Hall: ORCID iD orcid.org/0000-0001-8570-9374

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Date deposited: 30 Mar 2015 12:18
Last modified: 15 Mar 2024 03:38

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Contributors

Author: Nicholas Evennett
Author: Elisabetta Cerigioni
Author: Nigel J. Hall ORCID iD
Author: Agostino Pierro
Author: Simon Eaton

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