Assessment of redox state and biochemical parameters of salivary glands in rats treated with anti-obesity drug sibutramine hydrochloride

Objectives To investigate the effects of anti-obesity drug sibutramine hydrochloride (SB) on redox state and biochemical parameters in the salivary glands. Materials and methods Adult male Wistar rats were randomly divided into the following groups ( n  = 8 per group): control rats treated with vehi...

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Veröffentlicht in:Clinical oral investigations 2022-09, Vol.26 (9), p.5833-5846
Hauptverfasser: dos Santos, Damáris Raissa, Fiais, Gabriela Alice, Oliveira, Henrique Arnaldo, Ribas, Tayná Buffulin, Souza, Rayne Oliveira, Tsosura, Thaís Verônica Saori, Matsushita, Doris Hissako, Ervolino, Edilson, Dornelles, Rita Cássia Menegati, Nakamune, Ana Cláudia de Melo Stevanato, Chaves-Neto, Antonio Hernandes
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container_end_page 5846
container_issue 9
container_start_page 5833
container_title Clinical oral investigations
container_volume 26
creator dos Santos, Damáris Raissa
Fiais, Gabriela Alice
Oliveira, Henrique Arnaldo
Ribas, Tayná Buffulin
Souza, Rayne Oliveira
Tsosura, Thaís Verônica Saori
Matsushita, Doris Hissako
Ervolino, Edilson
Dornelles, Rita Cássia Menegati
Nakamune, Ana Cláudia de Melo Stevanato
Chaves-Neto, Antonio Hernandes
description Objectives To investigate the effects of anti-obesity drug sibutramine hydrochloride (SB) on redox state and biochemical parameters in the salivary glands. Materials and methods Adult male Wistar rats were randomly divided into the following groups ( n  = 8 per group): control rats treated with vehicle (C) and rats treated with SB (10 mg/kg/day) by intragastric gavage for 28 days. The parotid (PG) and submandibular (SMG) glands were processed using histomorphometric analysis, and total protein, amylase, mucin, and oxidative damage to lipids were determined by measuring the formation of thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), uric acid (UA), total glutathione (tGSH), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), and AKT phosphorylation. Results SB decreased the acinar area, and increased the stromal area in PG, while no effect on the morphometric parameters was observed in SMG. SB also increased oxidative damage to lipids (TBARs). The SB group showed lower total protein, amylase, TAC, UA, tGSH, SOD, CAT, and GPx than the C group in PG, while in SMG, SB decreased total protein, mucin, tGSH, SOD, CAT, and GPx. However, increased AKT phosphorylation observed in both salivary glands suggests that SB exerts low-intensity oxidative stress. Conclusions SB impaired enzymatic and non-enzymatic antioxidant defenses in the salivary glands of rats. Clinical relevance Chronic treatment with SB could mitigate salivary gland dysfunction due to disturbance of redox state.
doi_str_mv 10.1007/s00784-022-04539-1
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Materials and methods Adult male Wistar rats were randomly divided into the following groups ( n  = 8 per group): control rats treated with vehicle (C) and rats treated with SB (10 mg/kg/day) by intragastric gavage for 28 days. The parotid (PG) and submandibular (SMG) glands were processed using histomorphometric analysis, and total protein, amylase, mucin, and oxidative damage to lipids were determined by measuring the formation of thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), uric acid (UA), total glutathione (tGSH), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), and AKT phosphorylation. Results SB decreased the acinar area, and increased the stromal area in PG, while no effect on the morphometric parameters was observed in SMG. SB also increased oxidative damage to lipids (TBARs). The SB group showed lower total protein, amylase, TAC, UA, tGSH, SOD, CAT, and GPx than the C group in PG, while in SMG, SB decreased total protein, mucin, tGSH, SOD, CAT, and GPx. However, increased AKT phosphorylation observed in both salivary glands suggests that SB exerts low-intensity oxidative stress. Conclusions SB impaired enzymatic and non-enzymatic antioxidant defenses in the salivary glands of rats. Clinical relevance Chronic treatment with SB could mitigate salivary gland dysfunction due to disturbance of redox state.</description><identifier>ISSN: 1436-3771</identifier><identifier>ISSN: 1432-6981</identifier><identifier>EISSN: 1436-3771</identifier><identifier>DOI: 10.1007/s00784-022-04539-1</identifier><identifier>PMID: 35556176</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>AKT protein ; Antioxidants ; Catalase ; Dentistry ; Exocrine glands ; Glutathione peroxidase ; Lipids ; Medicine ; Mucin ; Obesity ; Original Article ; Oxidative stress ; Parotid gland ; Phosphorylation ; Proteins ; Redox properties ; Rodents ; Salivary gland ; Sibutramine ; Submandibular gland ; Superoxide dismutase ; Thiobarbituric acid ; Uric acid</subject><ispartof>Clinical oral investigations, 2022-09, Vol.26 (9), p.5833-5846</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c305t-64d93c37ff08efb84f6c5c9168e3b5876a3875e2cedd01854a48e3d3534241913</citedby><cites>FETCH-LOGICAL-c305t-64d93c37ff08efb84f6c5c9168e3b5876a3875e2cedd01854a48e3d3534241913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00784-022-04539-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00784-022-04539-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35556176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>dos Santos, Damáris Raissa</creatorcontrib><creatorcontrib>Fiais, Gabriela Alice</creatorcontrib><creatorcontrib>Oliveira, Henrique Arnaldo</creatorcontrib><creatorcontrib>Ribas, Tayná Buffulin</creatorcontrib><creatorcontrib>Souza, Rayne Oliveira</creatorcontrib><creatorcontrib>Tsosura, Thaís Verônica Saori</creatorcontrib><creatorcontrib>Matsushita, Doris Hissako</creatorcontrib><creatorcontrib>Ervolino, Edilson</creatorcontrib><creatorcontrib>Dornelles, Rita Cássia Menegati</creatorcontrib><creatorcontrib>Nakamune, Ana Cláudia de Melo Stevanato</creatorcontrib><creatorcontrib>Chaves-Neto, Antonio Hernandes</creatorcontrib><title>Assessment of redox state and biochemical parameters of salivary glands in rats treated with anti-obesity drug sibutramine hydrochloride</title><title>Clinical oral investigations</title><addtitle>Clin Oral Invest</addtitle><addtitle>Clin Oral Investig</addtitle><description>Objectives To investigate the effects of anti-obesity drug sibutramine hydrochloride (SB) on redox state and biochemical parameters in the salivary glands. Materials and methods Adult male Wistar rats were randomly divided into the following groups ( n  = 8 per group): control rats treated with vehicle (C) and rats treated with SB (10 mg/kg/day) by intragastric gavage for 28 days. The parotid (PG) and submandibular (SMG) glands were processed using histomorphometric analysis, and total protein, amylase, mucin, and oxidative damage to lipids were determined by measuring the formation of thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), uric acid (UA), total glutathione (tGSH), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), and AKT phosphorylation. Results SB decreased the acinar area, and increased the stromal area in PG, while no effect on the morphometric parameters was observed in SMG. SB also increased oxidative damage to lipids (TBARs). The SB group showed lower total protein, amylase, TAC, UA, tGSH, SOD, CAT, and GPx than the C group in PG, while in SMG, SB decreased total protein, mucin, tGSH, SOD, CAT, and GPx. However, increased AKT phosphorylation observed in both salivary glands suggests that SB exerts low-intensity oxidative stress. Conclusions SB impaired enzymatic and non-enzymatic antioxidant defenses in the salivary glands of rats. 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Materials and methods Adult male Wistar rats were randomly divided into the following groups ( n  = 8 per group): control rats treated with vehicle (C) and rats treated with SB (10 mg/kg/day) by intragastric gavage for 28 days. The parotid (PG) and submandibular (SMG) glands were processed using histomorphometric analysis, and total protein, amylase, mucin, and oxidative damage to lipids were determined by measuring the formation of thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), uric acid (UA), total glutathione (tGSH), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), and AKT phosphorylation. Results SB decreased the acinar area, and increased the stromal area in PG, while no effect on the morphometric parameters was observed in SMG. SB also increased oxidative damage to lipids (TBARs). The SB group showed lower total protein, amylase, TAC, UA, tGSH, SOD, CAT, and GPx than the C group in PG, while in SMG, SB decreased total protein, mucin, tGSH, SOD, CAT, and GPx. However, increased AKT phosphorylation observed in both salivary glands suggests that SB exerts low-intensity oxidative stress. Conclusions SB impaired enzymatic and non-enzymatic antioxidant defenses in the salivary glands of rats. Clinical relevance Chronic treatment with SB could mitigate salivary gland dysfunction due to disturbance of redox state.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35556176</pmid><doi>10.1007/s00784-022-04539-1</doi><tpages>14</tpages></addata></record>
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subjects AKT protein
Antioxidants
Catalase
Dentistry
Exocrine glands
Glutathione peroxidase
Lipids
Medicine
Mucin
Obesity
Original Article
Oxidative stress
Parotid gland
Phosphorylation
Proteins
Redox properties
Rodents
Salivary gland
Sibutramine
Submandibular gland
Superoxide dismutase
Thiobarbituric acid
Uric acid
title Assessment of redox state and biochemical parameters of salivary glands in rats treated with anti-obesity drug sibutramine hydrochloride
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