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Erschienen in: Digestive Diseases and Sciences 9/2019

01.04.2019 | Original Article

Can Sertraline and Nortriptyline Protect the Neurons in Submucosal and Myenteric Plexuses of Rat’s Colon Against Stress?

verfasst von: Ali Noorafshan, Majid Yousefi, Leila Hosseini, Saied Karbalay-Doust

Erschienen in: Digestive Diseases and Sciences | Ausgabe 9/2019

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Abstract

Background

The colon is partly controlled by myenteric and submucosal plexuses, which respond to stress and lead to some gastrointestinal disorders. These plexuses play roles in irritable bowel syndrome. Patients suffering from this syndrome can be treated with some antidepressants, including sertraline and nortriptyline.

Aims

The primary aim of study was to compare the effect of a sertraline and a nortriptyline on the structural changes of the enteric neurons after stress exposure in both sexes. The secondary objectives were to evaluate the effects of stress on the submucosal and myenteric plexuses.

Methods

Male and female Sprague-Dawley rats were assigned to four subgroups. The first subgroup received no stress. The other three subgroups received chronic variable stress (CVS) and were given phosphate buffer, sertraline (10 mg/kg/day), or nortriptyline (10 mg/kg/day). After 45 days, the neuron number in their colon plexuses was estimated using the stereologic method.

Results

The number of neurons increased by 40–51% in the submucosal plexus and by 57–69% in the myenteric plexus in the CVS group compared with the control group (p < 0.002) without any sex preference. The increment was significantly higher in the myenteric plexus than in the submucosal plexus (p < 0.05). Moreover, co-treatment of stressed rats with sertraline and nortriptyline could prevent the cellular hyperplasia of the plexuses, with more effective action for sertraline (p < 0.02).

Conclusions

Stress exposure for 45 days induced hyperplasia of the colon’s enteric plexuses in both sexes. However, these drugs could prevent the changes, with a more effective action for sertraline.
Literatur
1.
Zurück zum Zitat Konturek PC, Brzozowski T, Konturek SJ. Stress and the gut: pathophysiology, clinical consequences, diagnostic approach and treatment options. J Physiol Pharmacol. 2011;62:591–599.PubMed Konturek PC, Brzozowski T, Konturek SJ. Stress and the gut: pathophysiology, clinical consequences, diagnostic approach and treatment options. J Physiol Pharmacol. 2011;62:591–599.PubMed
2.
Zurück zum Zitat Saunders PR, Kosecka U, McKay DM, et al. Acute stressors stimulate ion secretion and increase epithelial permeability in rat intestine. Am J Physiol. 1994;267:G794–G799.PubMed Saunders PR, Kosecka U, McKay DM, et al. Acute stressors stimulate ion secretion and increase epithelial permeability in rat intestine. Am J Physiol. 1994;267:G794–G799.PubMed
10.
Zurück zum Zitat Hyde DM, Tyler NK, Plopper CG. Morphometry of the respiratory tract: avoiding the sampling, size, orientation, and reference traps. Toxicol Pathol. 2007;35:41–48.CrossRefPubMed Hyde DM, Tyler NK, Plopper CG. Morphometry of the respiratory tract: avoiding the sampling, size, orientation, and reference traps. Toxicol Pathol. 2007;35:41–48.CrossRefPubMed
11.
Zurück zum Zitat Noorafshan A, Abdollahifar MA, Karbalay-Doust S, et al. Sertraline and curcumin prevent stress-induced morphological changes of dendrites and neurons in the medial prefrontal cortex of rats. Folia Neuropathol. 2015;53:69–79.CrossRefPubMed Noorafshan A, Abdollahifar MA, Karbalay-Doust S, et al. Sertraline and curcumin prevent stress-induced morphological changes of dendrites and neurons in the medial prefrontal cortex of rats. Folia Neuropathol. 2015;53:69–79.CrossRefPubMed
12.
Zurück zum Zitat Bae SK, Yang KH, Aryal DK, et al. Pharmacokinetics of amitriptyline and one of its metabolites, nortriptyline, in rats: little contribution of considerable hepatic first-pass effect to low bioavailability of amitriptyline due to great intestinal first-pass effect. J Pharm Sci. 2009;98:1587–1601. https://doi.org/10.1002/jps.21511.CrossRefPubMed Bae SK, Yang KH, Aryal DK, et al. Pharmacokinetics of amitriptyline and one of its metabolites, nortriptyline, in rats: little contribution of considerable hepatic first-pass effect to low bioavailability of amitriptyline due to great intestinal first-pass effect. J Pharm Sci. 2009;98:1587–1601. https://​doi.​org/​10.​1002/​jps.​21511.CrossRefPubMed
18.
Zurück zum Zitat Gareau MG, Jury J, Perdue MH. Neonatal maternal separation of rat pups results in abnormal cholinergic regulation of epithelial permeability. Am J Physiol Gastrointest Liver Physiol. 2007;293:G198–G203.CrossRefPubMed Gareau MG, Jury J, Perdue MH. Neonatal maternal separation of rat pups results in abnormal cholinergic regulation of epithelial permeability. Am J Physiol Gastrointest Liver Physiol. 2007;293:G198–G203.CrossRefPubMed
Metadaten
Titel
Can Sertraline and Nortriptyline Protect the Neurons in Submucosal and Myenteric Plexuses of Rat’s Colon Against Stress?
verfasst von
Ali Noorafshan
Majid Yousefi
Leila Hosseini
Saied Karbalay-Doust
Publikationsdatum
01.04.2019
Verlag
Springer US
Erschienen in
Digestive Diseases and Sciences / Ausgabe 9/2019
Print ISSN: 0163-2116
Elektronische ISSN: 1573-2568
DOI
https://doi.org/10.1007/s10620-019-05600-y

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