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

• Published in: Clinical oral investigations Vol. 26; no. 9; pp. 5833 - 5846
• Main Authors: 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
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.09.2022; Springer Nature B.V
• 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; Submandibular gland; Oxidative stress; Anti-obesity agents; Sibutramine hydrochloride; Parotid gland
• ISSN: 1436-3771; 1432-6981; 1436-3771
• DOI: 10.1007/s00784-022-04539-1

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.