Syringic acid guards against indomethacin-induced gastric ulcer by alleviating inflammation, oxidative stress and apoptosis
Biotech Histochem. 2024 Apr 22:1-10. doi: 10.1080/10520295.2024.2344477. Online ahead of print.ABSTRACTThe purpose of this study was to evaluate the effects of syringic acid, an anti-oxidant, on indomethacin induced gastric ulcers in rats. Experimental groups were control, ulcer, ulcer treated with 20 mg/kg esomeprazole (a proton pump inhibitor that reduces acid secretion), and ulcer treated with 100 mg/kg syringic acid. Rats were pretreated with esomeprazole or syringic acid two weeks before ulcer induction. Our histopathological observations showed that either syringic acid or esomeprazole attenuated the severity of gast...
Source: Biotechnic and Histochemistry - April 22, 2024 Category: Research Authors: Irmak Ferah Okkay Ufuk Okkay Betul Cicek Ozhan Karatas Aysegul Yilmaz Fatma Yesilyurt Ahmet Hacimuftuoglu Source Type: research
Syringic acid guards against indomethacin-induced gastric ulcer by alleviating inflammation, oxidative stress and apoptosis
Biotech Histochem. 2024 Apr 22:1-10. doi: 10.1080/10520295.2024.2344477. Online ahead of print.ABSTRACTThe purpose of this study was to evaluate the effects of syringic acid, an anti-oxidant, on indomethacin induced gastric ulcers in rats. Experimental groups were control, ulcer, ulcer treated with 20 mg/kg esomeprazole (a proton pump inhibitor that reduces acid secretion), and ulcer treated with 100 mg/kg syringic acid. Rats were pretreated with esomeprazole or syringic acid two weeks before ulcer induction. Our histopathological observations showed that either syringic acid or esomeprazole attenuated the severity of gast...
Source: Biotechnic and Histochemistry - April 22, 2024 Category: Research Authors: Irmak Ferah Okkay Ufuk Okkay Betul Cicek Ozhan Karatas Aysegul Yilmaz Fatma Yesilyurt Ahmet Hacimuftuoglu Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Correction
Biotech Histochem. 2024 Apr 5:1. doi: 10.1080/10520295.2024.2335836. Online ahead of print.NO ABSTRACTPMID:38578171 | DOI:10.1080/10520295.2024.2335836 (Source: Biotechnic and Histochemistry)
Source: Biotechnic and Histochemistry - April 5, 2024 Category: Research Source Type: research
Nobiletin alleviates methotrexate-induced hepatorenal toxicity in rats
Biotech Histochem. 2024 Apr 2:1-13. doi: 10.1080/10520295.2024.2335168. Online ahead of print.ABSTRACTWe investigated the possible ameliorative effects of nobiletin (NBL) against methotrexate (MTX)-induced hepatorenal toxicity in rats. Twenty-eight Wistar albino rats were randomly divided into four groups, namely: Control; MTX (administered 20 mg/kg MTX); MTX+NBL (administered 20 mg/kg MTX and 10 mg/kg NBL per day); and NBL (administered 10 mg/kg/day NBL). Histopathological, immunohistochemical and biochemical analyses were performed on the kidney and liver tissues of rats at the end of the study. MTX caused renal toxicity...
Source: Biotechnic and Histochemistry - April 2, 2024 Category: Research Authors: Filiz Kazak Ahmet Uyar Pinar Coskun Turan Yaman Source Type: research
Nobiletin alleviates methotrexate-induced hepatorenal toxicity in rats
Biotech Histochem. 2024 Apr 2:1-13. doi: 10.1080/10520295.2024.2335168. Online ahead of print.ABSTRACTWe investigated the possible ameliorative effects of nobiletin (NBL) against methotrexate (MTX)-induced hepatorenal toxicity in rats. Twenty-eight Wistar albino rats were randomly divided into four groups, namely: Control; MTX (administered 20 mg/kg MTX); MTX+NBL (administered 20 mg/kg MTX and 10 mg/kg NBL per day); and NBL (administered 10 mg/kg/day NBL). Histopathological, immunohistochemical and biochemical analyses were performed on the kidney and liver tissues of rats at the end of the study. MTX caused renal toxicity...
Source: Biotechnic and Histochemistry - April 2, 2024 Category: Research Authors: Filiz Kazak Ahmet Uyar Pinar Coskun Turan Yaman Source Type: research
Nobiletin alleviates methotrexate-induced hepatorenal toxicity in rats
Biotech Histochem. 2024 Apr 2:1-13. doi: 10.1080/10520295.2024.2335168. Online ahead of print.ABSTRACTWe investigated the possible ameliorative effects of nobiletin (NBL) against methotrexate (MTX)-induced hepatorenal toxicity in rats. Twenty-eight Wistar albino rats were randomly divided into four groups, namely: Control; MTX (administered 20 mg/kg MTX); MTX+NBL (administered 20 mg/kg MTX and 10 mg/kg NBL per day); and NBL (administered 10 mg/kg/day NBL). Histopathological, immunohistochemical and biochemical analyses were performed on the kidney and liver tissues of rats at the end of the study. MTX caused renal toxicity...
Source: Biotechnic and Histochemistry - April 2, 2024 Category: Research Authors: Filiz Kazak Ahmet Uyar Pinar Coskun Turan Yaman Source Type: research
