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Gastroprophylactic Effects of p-Cymene in Ethanol-Induced Gastric Ulcer in Rats
The prevalence of gastric ulcers has increased in recent years, mainly because of non-steroidal anti-inflammatory drug utilization. Therefore, the current study investigates the gastroprotective effect of p-Cymene on absolute ethanol-induced acute gastric mucosal hemorrhagic lesions in rats. Thirty...
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Published in: | Processes 2022-07, Vol.10 (7), p.1314 |
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description | The prevalence of gastric ulcers has increased in recent years, mainly because of non-steroidal anti-inflammatory drug utilization. Therefore, the current study investigates the gastroprotective effect of p-Cymene on absolute ethanol-induced acute gastric mucosal hemorrhagic lesions in rats. Thirty Sprague Dawley rats were randomly separated into five groups: normal control, ulcer control, reference, and two experimental groups. The normal and ulcer control groups were orally fed with 0.5% carboxymethylcellulose (CMC). The reference group was fed orally with 20 mg/kg omeprazole. The experimental groups were fed with 30 mg/kg and 60 mg/kg p-Cymene, respectively. After one hour, the normal group was fed with 0.5% CMC, and groups 2–5 were given absolute alcohol. After another hour all rats were sacrificed. The ulcer control group showed severe superficial hemorrhagic gastric mucosal lesions with decreased gastric mucus secretion and pH of gastric content. p-Cymene significantly reduced ethanol-induced gastric lesions, as evidenced by increased mucus and pH of gastric content, decreased ulcer area, reduced or absence of edema, and leucocyte infiltration of the subcutaneous layer. In gastric mucosal homogenate, p-Cymene displayed a significant increase in superoxide dismutase (SOD), catalase (CAT) activities, prostaglandin E2 (PGE2), and significantly reduced the malondialdehyde (MDA) level. In addition, p-Cymene increased the intensity of periodic acid–Schiff (PAS) stain of the gastric epithelium, and produced up-regulation of the HSP 70 protein and down-regulation of the Bax protein of the stomach epithelium, as well as a reduction in the levels of tumor necrotic factor-alpha and interleukin-6, while the level of interleukin-10 was increased. p-Cymene decreased the level of TNF-a and IL-6, and increased the level of IL-10. Acute toxicity with a higher dose of 500 mg/kg p-Cymene did not manifest any toxicological signs in rats and could enhance defensive mechanisms against gastric mucosal lesions. p-Cymene showed gastroprotective effects that could be attributed to its antioxidant nature, or its ability to increase mucus secretion, increase endogenous enzymes (SOD, CAT, PGE2), reduce MDA level, up-regulate HSP 70 protein, down-regulate Bax protein, and modulate inflammatory cytokines. |
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F. ; Salehen, Nur Ain ; Ameen, Zeena M. ; Abdulla, Mahmood A.</creator><creatorcontrib>Shareef, Suhayla H. ; Al-Medhtiy, Morteta H. ; Ibrahim, Ibrahim Abdel Aziz ; Alzahrani, Abdullah R. ; Jabbar, Ahmed Aj ; Galali, Yaseen ; Agha, Nabaz Fisal Shakir ; Aziz, Peshawa Y. ; Thabit, Muthanna A. ; Agha, Derin N. F. ; Salehen, Nur Ain ; Ameen, Zeena M. ; Abdulla, Mahmood A.</creatorcontrib><description>The prevalence of gastric ulcers has increased in recent years, mainly because of non-steroidal anti-inflammatory drug utilization. Therefore, the current study investigates the gastroprotective effect of p-Cymene on absolute ethanol-induced acute gastric mucosal hemorrhagic lesions in rats. Thirty Sprague Dawley rats were randomly separated into five groups: normal control, ulcer control, reference, and two experimental groups. The normal and ulcer control groups were orally fed with 0.5% carboxymethylcellulose (CMC). The reference group was fed orally with 20 mg/kg omeprazole. The experimental groups were fed with 30 mg/kg and 60 mg/kg p-Cymene, respectively. After one hour, the normal group was fed with 0.5% CMC, and groups 2–5 were given absolute alcohol. After another hour all rats were sacrificed. The ulcer control group showed severe superficial hemorrhagic gastric mucosal lesions with decreased gastric mucus secretion and pH of gastric content. p-Cymene significantly reduced ethanol-induced gastric lesions, as evidenced by increased mucus and pH of gastric content, decreased ulcer area, reduced or absence of edema, and leucocyte infiltration of the subcutaneous layer. In gastric mucosal homogenate, p-Cymene displayed a significant increase in superoxide dismutase (SOD), catalase (CAT) activities, prostaglandin E2 (PGE2), and significantly reduced the malondialdehyde (MDA) level. In addition, p-Cymene increased the intensity of periodic acid–Schiff (PAS) stain of the gastric epithelium, and produced up-regulation of the HSP 70 protein and down-regulation of the Bax protein of the stomach epithelium, as well as a reduction in the levels of tumor necrotic factor-alpha and interleukin-6, while the level of interleukin-10 was increased. p-Cymene decreased the level of TNF-a and IL-6, and increased the level of IL-10. Acute toxicity with a higher dose of 500 mg/kg p-Cymene did not manifest any toxicological signs in rats and could enhance defensive mechanisms against gastric mucosal lesions. p-Cymene showed gastroprotective effects that could be attributed to its antioxidant nature, or its ability to increase mucus secretion, increase endogenous enzymes (SOD, CAT, PGE2), reduce MDA level, up-regulate HSP 70 protein, down-regulate Bax protein, and modulate inflammatory cytokines.</description><identifier>ISSN: 2227-9717</identifier><identifier>EISSN: 2227-9717</identifier><identifier>DOI: 10.3390/pr10071314</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acute toxicity ; Antioxidants ; BAX protein ; Carboxymethylcellulose ; Catalase ; Cold ; Cytokines ; Drinking water ; Drug dosages ; Edema ; Enzymes ; Epithelium ; Ethanol ; Free radicals ; Gastric mucosa ; Hemorrhage ; Herbal medicine ; Hsp70 protein ; Inflammation ; Interleukin 10 ; Interleukin 6 ; Laboratory animals ; Lesions ; Leukocytes ; Lipid peroxidation ; Manufacturers ; Metastases ; Mucus ; Omeprazole ; Oxidative stress ; p-Cymene ; pH effects ; Prostaglandin E2 ; Proteins ; Stomach ; Superoxide dismutase ; Toxicity ; Tumor necrosis factor-α ; Tumors ; Ulcers</subject><ispartof>Processes, 2022-07, Vol.10 (7), p.1314</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c295t-dadb8839f8b849a44e01cf53cbe115392799beebd9ba8c64a80e0a6e554bce233</citedby><cites>FETCH-LOGICAL-c295t-dadb8839f8b849a44e01cf53cbe115392799beebd9ba8c64a80e0a6e554bce233</cites><orcidid>0000-0001-9689-4018 ; 0000-0001-7782-0574 ; 0000-0002-5254-980X ; 0000-0001-5757-8653 ; 0000-0001-7212-959X ; 0000-0001-5346-4755</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2694071383/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2694071383?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Shareef, Suhayla H.</creatorcontrib><creatorcontrib>Al-Medhtiy, Morteta H.</creatorcontrib><creatorcontrib>Ibrahim, Ibrahim Abdel Aziz</creatorcontrib><creatorcontrib>Alzahrani, Abdullah R.</creatorcontrib><creatorcontrib>Jabbar, Ahmed Aj</creatorcontrib><creatorcontrib>Galali, Yaseen</creatorcontrib><creatorcontrib>Agha, Nabaz Fisal Shakir</creatorcontrib><creatorcontrib>Aziz, Peshawa Y.</creatorcontrib><creatorcontrib>Thabit, Muthanna A.</creatorcontrib><creatorcontrib>Agha, Derin N. F.</creatorcontrib><creatorcontrib>Salehen, Nur Ain</creatorcontrib><creatorcontrib>Ameen, Zeena M.</creatorcontrib><creatorcontrib>Abdulla, Mahmood A.</creatorcontrib><title>Gastroprophylactic Effects of p-Cymene in Ethanol-Induced Gastric Ulcer in Rats</title><title>Processes</title><description>The prevalence of gastric ulcers has increased in recent years, mainly because of non-steroidal anti-inflammatory drug utilization. Therefore, the current study investigates the gastroprotective effect of p-Cymene on absolute ethanol-induced acute gastric mucosal hemorrhagic lesions in rats. Thirty Sprague Dawley rats were randomly separated into five groups: normal control, ulcer control, reference, and two experimental groups. The normal and ulcer control groups were orally fed with 0.5% carboxymethylcellulose (CMC). The reference group was fed orally with 20 mg/kg omeprazole. The experimental groups were fed with 30 mg/kg and 60 mg/kg p-Cymene, respectively. After one hour, the normal group was fed with 0.5% CMC, and groups 2–5 were given absolute alcohol. After another hour all rats were sacrificed. The ulcer control group showed severe superficial hemorrhagic gastric mucosal lesions with decreased gastric mucus secretion and pH of gastric content. p-Cymene significantly reduced ethanol-induced gastric lesions, as evidenced by increased mucus and pH of gastric content, decreased ulcer area, reduced or absence of edema, and leucocyte infiltration of the subcutaneous layer. In gastric mucosal homogenate, p-Cymene displayed a significant increase in superoxide dismutase (SOD), catalase (CAT) activities, prostaglandin E2 (PGE2), and significantly reduced the malondialdehyde (MDA) level. In addition, p-Cymene increased the intensity of periodic acid–Schiff (PAS) stain of the gastric epithelium, and produced up-regulation of the HSP 70 protein and down-regulation of the Bax protein of the stomach epithelium, as well as a reduction in the levels of tumor necrotic factor-alpha and interleukin-6, while the level of interleukin-10 was increased. p-Cymene decreased the level of TNF-a and IL-6, and increased the level of IL-10. Acute toxicity with a higher dose of 500 mg/kg p-Cymene did not manifest any toxicological signs in rats and could enhance defensive mechanisms against gastric mucosal lesions. p-Cymene showed gastroprotective effects that could be attributed to its antioxidant nature, or its ability to increase mucus secretion, increase endogenous enzymes (SOD, CAT, PGE2), reduce MDA level, up-regulate HSP 70 protein, down-regulate Bax protein, and modulate inflammatory cytokines.</description><subject>Acute toxicity</subject><subject>Antioxidants</subject><subject>BAX protein</subject><subject>Carboxymethylcellulose</subject><subject>Catalase</subject><subject>Cold</subject><subject>Cytokines</subject><subject>Drinking water</subject><subject>Drug dosages</subject><subject>Edema</subject><subject>Enzymes</subject><subject>Epithelium</subject><subject>Ethanol</subject><subject>Free radicals</subject><subject>Gastric mucosa</subject><subject>Hemorrhage</subject><subject>Herbal medicine</subject><subject>Hsp70 protein</subject><subject>Inflammation</subject><subject>Interleukin 10</subject><subject>Interleukin 6</subject><subject>Laboratory animals</subject><subject>Lesions</subject><subject>Leukocytes</subject><subject>Lipid peroxidation</subject><subject>Manufacturers</subject><subject>Metastases</subject><subject>Mucus</subject><subject>Omeprazole</subject><subject>Oxidative stress</subject><subject>p-Cymene</subject><subject>pH effects</subject><subject>Prostaglandin E2</subject><subject>Proteins</subject><subject>Stomach</subject><subject>Superoxide dismutase</subject><subject>Toxicity</subject><subject>Tumor necrosis factor-α</subject><subject>Tumors</subject><subject>Ulcers</subject><issn>2227-9717</issn><issn>2227-9717</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpNkEtLw0AQgBdRsNRe_AUBb8LqvpLsHiXUtlAoiD2H3c0sTUmTuLs55N-bWEGHgZnDNw8-hB4peeFckdfeU0Jyyqm4QQvGWI5VTvPbf_09WoVwJlMoymWaLdBho0P0XT_laWy0jbVN1s6BjSHpXNLjYrxAC0ndJut40m3X4F1bDRaq5Gdywo-NBT8DHzqGB3TndBNg9VuX6Pi-_iy2eH_Y7Iq3PbZMpRFXujJScuWkkUJpIYBQ61JuDVCacsVypQyAqZTR0mZCSwJEZ5CmwlhgnC_R03Xv9PnXACGW527w7XSyZJkSswY5U89XyvouBA-u7H190X4sKSlnZ-WfM_4NXK5ePQ</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Shareef, Suhayla H.</creator><creator>Al-Medhtiy, Morteta H.</creator><creator>Ibrahim, Ibrahim Abdel Aziz</creator><creator>Alzahrani, Abdullah R.</creator><creator>Jabbar, Ahmed Aj</creator><creator>Galali, Yaseen</creator><creator>Agha, Nabaz Fisal Shakir</creator><creator>Aziz, Peshawa Y.</creator><creator>Thabit, Muthanna A.</creator><creator>Agha, Derin N. 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F.</creatorcontrib><creatorcontrib>Salehen, Nur Ain</creatorcontrib><creatorcontrib>Ameen, Zeena M.</creatorcontrib><creatorcontrib>Abdulla, Mahmood A.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Materials science collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Processes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shareef, Suhayla H.</au><au>Al-Medhtiy, Morteta H.</au><au>Ibrahim, Ibrahim Abdel Aziz</au><au>Alzahrani, Abdullah R.</au><au>Jabbar, Ahmed Aj</au><au>Galali, Yaseen</au><au>Agha, Nabaz Fisal Shakir</au><au>Aziz, Peshawa Y.</au><au>Thabit, Muthanna A.</au><au>Agha, Derin N. F.</au><au>Salehen, Nur Ain</au><au>Ameen, Zeena M.</au><au>Abdulla, Mahmood A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gastroprophylactic Effects of p-Cymene in Ethanol-Induced Gastric Ulcer in Rats</atitle><jtitle>Processes</jtitle><date>2022-07-01</date><risdate>2022</risdate><volume>10</volume><issue>7</issue><spage>1314</spage><pages>1314-</pages><issn>2227-9717</issn><eissn>2227-9717</eissn><abstract>The prevalence of gastric ulcers has increased in recent years, mainly because of non-steroidal anti-inflammatory drug utilization. Therefore, the current study investigates the gastroprotective effect of p-Cymene on absolute ethanol-induced acute gastric mucosal hemorrhagic lesions in rats. Thirty Sprague Dawley rats were randomly separated into five groups: normal control, ulcer control, reference, and two experimental groups. The normal and ulcer control groups were orally fed with 0.5% carboxymethylcellulose (CMC). The reference group was fed orally with 20 mg/kg omeprazole. The experimental groups were fed with 30 mg/kg and 60 mg/kg p-Cymene, respectively. After one hour, the normal group was fed with 0.5% CMC, and groups 2–5 were given absolute alcohol. After another hour all rats were sacrificed. The ulcer control group showed severe superficial hemorrhagic gastric mucosal lesions with decreased gastric mucus secretion and pH of gastric content. p-Cymene significantly reduced ethanol-induced gastric lesions, as evidenced by increased mucus and pH of gastric content, decreased ulcer area, reduced or absence of edema, and leucocyte infiltration of the subcutaneous layer. In gastric mucosal homogenate, p-Cymene displayed a significant increase in superoxide dismutase (SOD), catalase (CAT) activities, prostaglandin E2 (PGE2), and significantly reduced the malondialdehyde (MDA) level. In addition, p-Cymene increased the intensity of periodic acid–Schiff (PAS) stain of the gastric epithelium, and produced up-regulation of the HSP 70 protein and down-regulation of the Bax protein of the stomach epithelium, as well as a reduction in the levels of tumor necrotic factor-alpha and interleukin-6, while the level of interleukin-10 was increased. p-Cymene decreased the level of TNF-a and IL-6, and increased the level of IL-10. Acute toxicity with a higher dose of 500 mg/kg p-Cymene did not manifest any toxicological signs in rats and could enhance defensive mechanisms against gastric mucosal lesions. p-Cymene showed gastroprotective effects that could be attributed to its antioxidant nature, or its ability to increase mucus secretion, increase endogenous enzymes (SOD, CAT, PGE2), reduce MDA level, up-regulate HSP 70 protein, down-regulate Bax protein, and modulate inflammatory cytokines.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/pr10071314</doi><orcidid>https://orcid.org/0000-0001-9689-4018</orcidid><orcidid>https://orcid.org/0000-0001-7782-0574</orcidid><orcidid>https://orcid.org/0000-0002-5254-980X</orcidid><orcidid>https://orcid.org/0000-0001-5757-8653</orcidid><orcidid>https://orcid.org/0000-0001-7212-959X</orcidid><orcidid>https://orcid.org/0000-0001-5346-4755</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute toxicity Antioxidants BAX protein Carboxymethylcellulose Catalase Cold Cytokines Drinking water Drug dosages Edema Enzymes Epithelium Ethanol Free radicals Gastric mucosa Hemorrhage Herbal medicine Hsp70 protein Inflammation Interleukin 10 Interleukin 6 Laboratory animals Lesions Leukocytes Lipid peroxidation Manufacturers Metastases Mucus Omeprazole Oxidative stress p-Cymene pH effects Prostaglandin E2 Proteins Stomach Superoxide dismutase Toxicity Tumor necrosis factor-α Tumors Ulcers |
title | Gastroprophylactic Effects of p-Cymene in Ethanol-Induced Gastric Ulcer in Rats |
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