Effects of orchiectomy and testosterone replacement therapy on redox balance and salivary gland function in Wistar rats

•Orchiectomy induced salivary gland dysfunction.•Orchiectomy changes salivary secretion of total protein, amylase, and electrolytes.•Orchiectomy increases oxidative damage markers in the salivary gland.•Testosterone hormonal therapy restored salivary gland function.•Testosterone hormonal therapy res...

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Veröffentlicht in:The Journal of steroid biochemistry and molecular biology 2022-04, Vol.218, p.106048-106048, Article 106048
Hauptverfasser: dos Santos, Damáris Raissa, Fiais, Gabriela Alice, de Oliveira Passos, Arthur, dos Santos, Luis Fernando Gadioli, Kayahara, Giseli Mitsuy, Crivelini, Marcelo Macedo, Matsushita, Doris Hissako, Antoniali, Cristina, Nakamune, Ana Cláudia de Melo Stevanato, Dornelles, Rita Cássia Menegati, Chaves-Neto, Antonio Hernandes
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container_title The Journal of steroid biochemistry and molecular biology
container_volume 218
creator dos Santos, Damáris Raissa
Fiais, Gabriela Alice
de Oliveira Passos, Arthur
dos Santos, Luis Fernando Gadioli
Kayahara, Giseli Mitsuy
Crivelini, Marcelo Macedo
Matsushita, Doris Hissako
Antoniali, Cristina
Nakamune, Ana Cláudia de Melo Stevanato
Dornelles, Rita Cássia Menegati
Chaves-Neto, Antonio Hernandes
description •Orchiectomy induced salivary gland dysfunction.•Orchiectomy changes salivary secretion of total protein, amylase, and electrolytes.•Orchiectomy increases oxidative damage markers in the salivary gland.•Testosterone hormonal therapy restored salivary gland function.•Testosterone hormonal therapy restored redox balance of the salivary gland. The objective of this study was to investigate the effects of orchiectomy (ORX) and testosterone replacement therapy (TRT) on redox balance and function of salivary glands. Forty-five young adult male Wistar rats (3 months old) were either castrated bilaterally or underwent fictitious surgery (SHAM) and were subsequently distributed into 3 groups: SHAM, ORX, and TRT (castrated rats that received an intramuscular injection of testosterone cypionate 10 mg/kg/weekly). All treatments started 4 weeks after castration (4 months old) and lasted 4 weeks (5 months old). At the end of treatment, pilocarpine-induced salivary secretion was collected to analyze salivary flow rate and biochemistry composition, and the parotid (PG) and submandibular (SMG) glands were sampled for redox balance markers and histomorphometric analyses. ORX increased salivary flow rate, calcium, phosphate, and chloride, and decreased total protein and amylase, while not changing the salivary buffer capacity, pH, sodium, and potassium compared to SHAM. TRT restored all salivary parameters to SHAM values. ORX increased oxidative lipid and protein damage, total antioxidant capacity, and uric acid in both salivary glands compared to SHAM. Superoxide dismutase, catalase, and glutathione peroxidase activities were greater only in the SMG of the ORX group in relation to SHAM. ORX decreased duct and acini area, while increasing connective tissue in the PG. On the other hand, ORX reduced duct area and increased acini area in the SMG compared to SHAM. TRT restored the redox balance and histomorphometric parameters to close to SHAM values in both salivary glands. Orchiectomy-induced salivary gland dysfunction was characterized by an increase in the salivary flow rate and changes in the secretion of total protein, amylase, and electrolytes, which are key factors, considered important for maintaining oral health status. To sum up, orchiectomy impaired the redox balance of the salivary glands. Our results also showed that TRT reversed the oxidative damage, morphological alterations, and salivary gland dysfunction induced by orchiectomy. Therefore, these results suggest
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The objective of this study was to investigate the effects of orchiectomy (ORX) and testosterone replacement therapy (TRT) on redox balance and function of salivary glands. Forty-five young adult male Wistar rats (3 months old) were either castrated bilaterally or underwent fictitious surgery (SHAM) and were subsequently distributed into 3 groups: SHAM, ORX, and TRT (castrated rats that received an intramuscular injection of testosterone cypionate 10 mg/kg/weekly). All treatments started 4 weeks after castration (4 months old) and lasted 4 weeks (5 months old). At the end of treatment, pilocarpine-induced salivary secretion was collected to analyze salivary flow rate and biochemistry composition, and the parotid (PG) and submandibular (SMG) glands were sampled for redox balance markers and histomorphometric analyses. ORX increased salivary flow rate, calcium, phosphate, and chloride, and decreased total protein and amylase, while not changing the salivary buffer capacity, pH, sodium, and potassium compared to SHAM. TRT restored all salivary parameters to SHAM values. ORX increased oxidative lipid and protein damage, total antioxidant capacity, and uric acid in both salivary glands compared to SHAM. Superoxide dismutase, catalase, and glutathione peroxidase activities were greater only in the SMG of the ORX group in relation to SHAM. ORX decreased duct and acini area, while increasing connective tissue in the PG. On the other hand, ORX reduced duct area and increased acini area in the SMG compared to SHAM. TRT restored the redox balance and histomorphometric parameters to close to SHAM values in both salivary glands. Orchiectomy-induced salivary gland dysfunction was characterized by an increase in the salivary flow rate and changes in the secretion of total protein, amylase, and electrolytes, which are key factors, considered important for maintaining oral health status. To sum up, orchiectomy impaired the redox balance of the salivary glands. Our results also showed that TRT reversed the oxidative damage, morphological alterations, and salivary gland dysfunction induced by orchiectomy. Therefore, these results suggest an important action of testosterone on the redox balance and secretory ability of salivary glands.</description><identifier>ISSN: 0960-0760</identifier><identifier>EISSN: 1879-1220</identifier><identifier>DOI: 10.1016/j.jsbmb.2021.106048</identifier><identifier>PMID: 34973376</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Amylases - metabolism ; Animals ; Antioxidants ; Antioxidants - metabolism ; Antioxidants - pharmacology ; Calcium chloride ; Calcium phosphates ; Castration ; Catalase ; Connective tissues ; Exocrine glands ; Glutathione peroxidase ; Hormone replacement therapy ; Male ; Orchiectomy ; Oxidation-Reduction ; Oxidative stress ; Pilocarpine ; Proteins ; Rats ; Rats, Wistar ; Rodents ; Saliva ; Salivary gland ; Salivary glands ; Salivary Glands - metabolism ; Secretion ; Superoxide dismutase ; Testosterone ; Testosterone - metabolism ; Testosterone cypionate ; Uric acid</subject><ispartof>The Journal of steroid biochemistry and molecular biology, 2022-04, Vol.218, p.106048-106048, Article 106048</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier BV Apr 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-9371bd00e3c5780fb8b5e9db5e22757ee1ea55daf97a2be1042de6ea1a5ada5b3</citedby><cites>FETCH-LOGICAL-c387t-9371bd00e3c5780fb8b5e9db5e22757ee1ea55daf97a2be1042de6ea1a5ada5b3</cites><orcidid>0000-0001-6481-5506 ; 0000-0002-0174-439X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0960076021002417$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34973376$$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>de Oliveira Passos, Arthur</creatorcontrib><creatorcontrib>dos Santos, Luis Fernando Gadioli</creatorcontrib><creatorcontrib>Kayahara, Giseli Mitsuy</creatorcontrib><creatorcontrib>Crivelini, Marcelo Macedo</creatorcontrib><creatorcontrib>Matsushita, Doris Hissako</creatorcontrib><creatorcontrib>Antoniali, Cristina</creatorcontrib><creatorcontrib>Nakamune, Ana Cláudia de Melo Stevanato</creatorcontrib><creatorcontrib>Dornelles, Rita Cássia Menegati</creatorcontrib><creatorcontrib>Chaves-Neto, Antonio Hernandes</creatorcontrib><title>Effects of orchiectomy and testosterone replacement therapy on redox balance and salivary gland function in Wistar rats</title><title>The Journal of steroid biochemistry and molecular biology</title><addtitle>J Steroid Biochem Mol Biol</addtitle><description>•Orchiectomy induced salivary gland dysfunction.•Orchiectomy changes salivary secretion of total protein, amylase, and electrolytes.•Orchiectomy increases oxidative damage markers in the salivary gland.•Testosterone hormonal therapy restored salivary gland function.•Testosterone hormonal therapy restored redox balance of the salivary gland. The objective of this study was to investigate the effects of orchiectomy (ORX) and testosterone replacement therapy (TRT) on redox balance and function of salivary glands. Forty-five young adult male Wistar rats (3 months old) were either castrated bilaterally or underwent fictitious surgery (SHAM) and were subsequently distributed into 3 groups: SHAM, ORX, and TRT (castrated rats that received an intramuscular injection of testosterone cypionate 10 mg/kg/weekly). All treatments started 4 weeks after castration (4 months old) and lasted 4 weeks (5 months old). At the end of treatment, pilocarpine-induced salivary secretion was collected to analyze salivary flow rate and biochemistry composition, and the parotid (PG) and submandibular (SMG) glands were sampled for redox balance markers and histomorphometric analyses. ORX increased salivary flow rate, calcium, phosphate, and chloride, and decreased total protein and amylase, while not changing the salivary buffer capacity, pH, sodium, and potassium compared to SHAM. TRT restored all salivary parameters to SHAM values. ORX increased oxidative lipid and protein damage, total antioxidant capacity, and uric acid in both salivary glands compared to SHAM. Superoxide dismutase, catalase, and glutathione peroxidase activities were greater only in the SMG of the ORX group in relation to SHAM. ORX decreased duct and acini area, while increasing connective tissue in the PG. On the other hand, ORX reduced duct area and increased acini area in the SMG compared to SHAM. TRT restored the redox balance and histomorphometric parameters to close to SHAM values in both salivary glands. Orchiectomy-induced salivary gland dysfunction was characterized by an increase in the salivary flow rate and changes in the secretion of total protein, amylase, and electrolytes, which are key factors, considered important for maintaining oral health status. To sum up, orchiectomy impaired the redox balance of the salivary glands. Our results also showed that TRT reversed the oxidative damage, morphological alterations, and salivary gland dysfunction induced by orchiectomy. 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The objective of this study was to investigate the effects of orchiectomy (ORX) and testosterone replacement therapy (TRT) on redox balance and function of salivary glands. Forty-five young adult male Wistar rats (3 months old) were either castrated bilaterally or underwent fictitious surgery (SHAM) and were subsequently distributed into 3 groups: SHAM, ORX, and TRT (castrated rats that received an intramuscular injection of testosterone cypionate 10 mg/kg/weekly). All treatments started 4 weeks after castration (4 months old) and lasted 4 weeks (5 months old). At the end of treatment, pilocarpine-induced salivary secretion was collected to analyze salivary flow rate and biochemistry composition, and the parotid (PG) and submandibular (SMG) glands were sampled for redox balance markers and histomorphometric analyses. ORX increased salivary flow rate, calcium, phosphate, and chloride, and decreased total protein and amylase, while not changing the salivary buffer capacity, pH, sodium, and potassium compared to SHAM. TRT restored all salivary parameters to SHAM values. ORX increased oxidative lipid and protein damage, total antioxidant capacity, and uric acid in both salivary glands compared to SHAM. Superoxide dismutase, catalase, and glutathione peroxidase activities were greater only in the SMG of the ORX group in relation to SHAM. ORX decreased duct and acini area, while increasing connective tissue in the PG. On the other hand, ORX reduced duct area and increased acini area in the SMG compared to SHAM. TRT restored the redox balance and histomorphometric parameters to close to SHAM values in both salivary glands. Orchiectomy-induced salivary gland dysfunction was characterized by an increase in the salivary flow rate and changes in the secretion of total protein, amylase, and electrolytes, which are key factors, considered important for maintaining oral health status. To sum up, orchiectomy impaired the redox balance of the salivary glands. Our results also showed that TRT reversed the oxidative damage, morphological alterations, and salivary gland dysfunction induced by orchiectomy. Therefore, these results suggest an important action of testosterone on the redox balance and secretory ability of salivary glands.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>34973376</pmid><doi>10.1016/j.jsbmb.2021.106048</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6481-5506</orcidid><orcidid>https://orcid.org/0000-0002-0174-439X</orcidid></addata></record>
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ispartof The Journal of steroid biochemistry and molecular biology, 2022-04, Vol.218, p.106048-106048, Article 106048
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subjects Amylases - metabolism
Animals
Antioxidants
Antioxidants - metabolism
Antioxidants - pharmacology
Calcium chloride
Calcium phosphates
Castration
Catalase
Connective tissues
Exocrine glands
Glutathione peroxidase
Hormone replacement therapy
Male
Orchiectomy
Oxidation-Reduction
Oxidative stress
Pilocarpine
Proteins
Rats
Rats, Wistar
Rodents
Saliva
Salivary gland
Salivary glands
Salivary Glands - metabolism
Secretion
Superoxide dismutase
Testosterone
Testosterone - metabolism
Testosterone cypionate
Uric acid
title Effects of orchiectomy and testosterone replacement therapy on redox balance and salivary gland function in Wistar rats
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