Evidence map›Paper›PMID 24653522›Full record

ArticleCurrent therapeutic research, clinical and experimental2012

Analysis of the protective biochemical and pathologic effects of aminoguanidine on an experimental aspiration pneumonitis model induced by bile acids.

Rifat Karli, Hasan Alacam, Latif Duran, Omer Alici, Celal Kati, Arzu Karli, Ahmet Guzel

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Article in Current therapeutic research, clinical and experimental, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Rifat KarliDepartment of Otorhinolaryngology, Ondokuz Mayis University, Samsun, Turkey.
Hasan AlacamDepartment of Medical Biochemistry, Ondokuz Mayis University, Samsun, Turkey.
Latif DuranDepartment of Emergency Medicine, Ondokuz Mayis University, Samsun, Turkey.
Omer AliciDepartment of Pathology, Samsun Education and Research Hospital, Samsun, Turkey.
Celal KatiDepartment of Otorhinolaryngology, Ondokuz Mayis University, Samsun, Turkey.
Arzu KarliDepartment of Pediatric Infection, Ondokuz Mayis University, Samsun, Turkey.
Ahmet GuzelDepartment of Pediatrics, Ondokuz Mayis University, Samsun, Turkey.
Ondokuz Mayıs University · TRSamsun University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastroesophageal reflux (GER) is a common clinical pathology detected in childhood. Bile acids (BAs) are present in reflux and cause various pathologies in the esophagus, the larynx, and the lungs.

objectiveWe aimed to show if aminoguanidine (AG) contributes to the biochemical and histopathologic treatment of experimental aspiration pneumonitis induced by BAs.

methodsTwenty-eight female Sprague Dawley rats were used. There were 4 groups in the study: (1) group aspirated with 0.9% saline (n = 7), (2) group aspirated with 0.9% saline and treated with AG (n = 7), (3) group aspirated with a solution of 10 mg/kg taurocholic acid and 5 mg/kg taurochenodeoxycholate (n = 7), and (4) group aspirated with BA and treated with AG (n = 7). The saline and BA solutions were administered as 1 mL/kg intratracheally. The AG was administered intraperitoneally twice a day at a 150 mg/kg dose for 7 days. The different histopathologic and biochemical parameters were analyzed.

resultsClara cell protein 16 and malondialdehyde levels were found to be significantly higher in the BA group than in the group where saline was administered; however, they were significantly lower in the BA + AG group than in the BA group. The total superoxide dismutase activity decreased significantly in the BA group compared with the group where saline was administered. A significant increase in superoxide dismutase activity was observed in the BA + AG group when compared with the group where only BA was administered. When the group where BA was administered solely was compared with the group where saline was administered, peribronchial inflammatory cell infiltration, alveolar septal infiltration, alveolar histiocytes, interstitial fibrosis, and granuloma were significantly higher in the BA group than in the saline group. When the BA + AG group was compared with the BA group, peribronchial inflammatory cell infiltration, alveolar septal infiltration, alveolar histiocytes, interstitial fibrosis, and granuloma were found to be significantly lower.

conclusionsOxidant stress increases and antioxidant capacity decreases in pneumonitis induced by BAs. AG administration as an antioxidant helps in recovery, both biochemically and histopathologically. Consequently, AG seems to be an alternative that should be considered in a conservative approach to treating aspiration pneumonitis.

Indexed as

aminoguanidineaspiration pneumonitisbile acidsCC-16gastroesophageal reflux

Identifiers

PMID24653522
PMCPMC3955109
OpenAlexW1994569650

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.