dc.creatorBrandelero Jr. S.
dc.creatorBonfleur M.L.
dc.creatorRibeiro R.A.
dc.creatorVanzela E.C.
dc.creatorNassar C.A.
dc.creatorNassar P.O.
dc.creatorBalbo S.L.
dc.date2012
dc.date2015-06-25T20:24:21Z
dc.date2015-11-26T15:19:54Z
dc.date2015-06-25T20:24:21Z
dc.date2015-11-26T15:19:54Z
dc.date.accessioned2018-03-28T22:29:23Z
dc.date.available2018-03-28T22:29:23Z
dc.identifier
dc.identifierArchives Of Oral Biology. , v. 57, n. 3, p. 300 - 306, 2012.
dc.identifier39969
dc.identifier10.1016/j.archoralbio.2011.08.024
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84857633621&partnerID=40&md5=962730c21c383a2300169687d3015cd6
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/90203
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/90203
dc.identifier2-s2.0-84857633621
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1259848
dc.descriptionThe prevalence of obesity is increasing globally. There is evidence that the uncontrolled energetic metabolism in obese patients can accelerate periodontal disease. Therefore, the aim of this study was evaluate the possible relationship between hypothalamic obesity induced by neonatal treatment with MSG and experimental periodontal disease. Newborn male Wistar rats received subcutaneous injections in the cervical region, of 4g/Kg/day of body weight (BW) of MSG (MSG group) or hypertonic saline solution, 1.25/kg/day BW (control group, CTL). At 70 days of life periodontal disease was induced in these animals. After they were sacrificed, radiographic analyses of alveolar bone resorption and Tumor Necrosis Factor α (TNFα) gene expression in gingival tissue were performed. The neonatal treatment with MSG did not affect the concentration of plasma glucose and cholesterol (CHOL). However, plasma insulin, non-esterified fatty acids (NEFA) and triglycerides (TG) leves were higher in MSG compared with CTL group. The alveolar bone resorption was 44% lower in MSG-obese rats compared with CTL rats. In the presence of periodontal ligature, there was an increase in this parameter in all groups. The TNFα gene expression, an inflammatory marker, in periodontal tissue was similar in obese and CTL rats. The presence of ligature increased TNFα gene expression in both groups, but in a lower extension in MSG-obese rats. In conclusion these results suggested that hypothalamic obesity may produce a protective effect against periodontal disease, however further research is needed to understand the mechanisms involved in this process. © 2011 Elsevier Ltd.
dc.description57
dc.description3
dc.description300
dc.description306
dc.descriptionLosche, W., Karapetow, F., Pohl, A., Pohl, C., Kocher, T., Plasma lipid and blood glucose levels in patients with destructive periodontal disease (2000) J Clin Periodontol, 27, pp. 537-541
dc.descriptionIacopino, A.M., Periodontitis and diabetes interrelationships: Role of inflammation (2001) Ann Periodontol, 6, pp. 125-137
dc.descriptionPerlstein, M.I., Bissada, N.F., Influence of obesity and hypertension on the severity of periodontitis in rats (1977) Oral Surgery Oral Medicine and Oral Pathology, 43 (5), pp. 707-719
dc.descriptionSaito, T., Murakami, M., Shimazaki, Y., Oobayashi, K., Matsumoto, S., Koga, T., Association between alveolar bone loss and elevated serum C-reactive protein in Japanese men (2003) Journal of Periodontology, 74 (12), pp. 1741-1746. , DOI 10.1902/jop.2003.74.12.1741
dc.descriptionAl-Zahrani, M.S., Bissada, N.F., Borawski, E.A., Obesity and periodontal disease in young, middle-aged, and older adults (2003) Journal of Periodontology, 74 (5), pp. 610-615. , DOI 10.1902/jop.2003.74.5.610
dc.descriptionOrban, Z., Remaley, A.T., Sampson, M., Trajanoski, Z., Chrousos, G.P., The differential effect of food intake and β-adrenergic stimulation on adipose-derived hormones and cytokines in man (1999) Journal of Clinical Endocrinology and Metabolism, 84 (6), pp. 2126-2133
dc.descriptionNishimura, F., Murayama, Y., Periodontal inflammation and insulin resistance - Lessons from obesity (2001) Journal of Dental Research, 80 (8), pp. 1690-1694
dc.descriptionZhao, Y.F., Chen, C., Regulation of pancreatic beta-cell function by adipocytes (2007) Sheng Li Xue Bao, 59, pp. 247-252
dc.descriptionSantos, L.C., Cintra, I.P., Fisberg, M., Castro, M.L., Martini, L.A., Association among weight loss, bone mass, body composition and dietary intake of post-pubertal obese adolescents (2008) Arq Bras Endocrinol Metabol, 52, pp. 1001-1008
dc.descriptionLeonard, M.B., Shults, J., Wilson, B.A., Tershakovec, A.M., Zemel, B.S., Obesity during childhood and adolescence augments bone mass and bone dimensions (2004) Am J Clin Nutr, 80, pp. 514-523
dc.descriptionKontogianni, M.D., Dafni, U.G., Routsias, J.G., Skopouli, F.N., Blood leptin and adiponectin as possible mediators of the relation between fat mass and BMD in perimenopausal women (2004) Journal of Bone and Mineral Research, 19 (4), pp. 546-551. , DOI 10.1359/JBMR.040107
dc.descriptionReid, I.R., Cornish, J., Baldock, P.A., Nutrition-related peptides and bone homeostasis (2006) J Bone Miner Res, 21, pp. 495-500
dc.descriptionBlain, H., Vuillemin, A., Guillemin, F., Durant, R., Hanesse, B., De Talance, N., Doucet, B., Jeandel, C., Serum leptin level is a predictor of bone mineral density in postmenopausal women (2002) Journal of Clinical Endocrinology and Metabolism, 87 (3), pp. 1030-1035. , DOI 10.1210/jc.87.3.1030
dc.descriptionOlney, J.W., Adamo, N.J., Ratner, A., Monosodium glutamate effects (1971) Science, 172, p. 294
dc.descriptionOlney, J.W., Sharpe, L.G., Brain lesions in an infant rhesus monkey treated with monsodium glutamate (1969) Science, 166, pp. 386-388
dc.descriptionHolloway, W.R., Collier, F.Mc.L., Aitken, C.J., Myers, D.E., Hodge, J.M., Malakellis, M., Gough, T.J., Nicholson, G.C., Leptin inhibits osteoclast generation (2002) Journal of Bone and Mineral Research, 17 (2), pp. 200-209
dc.descriptionScallet, A.C., Olney, J.W., Components of hypothalamic obesity: Bipiperidyl-mustard lesions add hyperphagia to monosodium glutamate-induced hyperinsulinemia (1986) Brain Research, 374 (2), pp. 380-384. , DOI 10.1016/0006-8993(86)90434-8
dc.descriptionMaiter, D., Underwood, L.E., Martin, J.B., Koenig, J.I., Neonatal treatment with monosodium glutamate: Effects of prolonged growth hormone (GH)-releasing hormone deficiency on pulsatile GH secretion and growth in female rats (1991) Endocrinology, 128, pp. 1100-1106
dc.descriptionArndt, T., Rehorek, A., Muller, F., Assessment of cold induced alterations in catecholamine turnover of lean and glutamate-treated obese rats (1991) Exp Clin Endocrinol, 98, pp. 207-211
dc.descriptionBalbo, S., Grassiolli, S., Ribeiro, R., Bonfleur, M., Gravena, C., Brito, M., Andreazzi, A., Torrezan, R., Fat storage is partially dependent on vagal activity and insulin secretion of hypothalamic obese rat (2007) Endocrine, 31 (2), pp. 142-148. , DOI 10.1007/s12020-007-0021-z
dc.descriptionBalbo, S.L., De Freitas Mathias, P.C., Bonfleur, M.L., Alves, H.F., Siroti, F.J., Gomes Monteiro, O., Borges Ribeiro, F., Da Silva Fernando Souza, A.C.M., Vagotomy reduces obesity in MSG-treated rats (2000) Research Communications in Molecular Pathology and Pharmacology, 108 (5-6), pp. 291-296
dc.descriptionIwase, M., Ichikawa, K., Tashiro, K., Iino, K., Shinohara, N., Ibayashi, S., Effects of monosodium glutamate-induced obesity in spontaneously hypertensive rats vs. Wistar Kyoto rats: Serum leptin and blood flow to brown adipose tissue (2000) Hypertens Res, 23, pp. 503-510
dc.descriptionNassar, C.A., Nassar, P.O., Abi Rached, R.S.G., Holzhausen, M., Marcantonio Jr., E., Spolidorio, L.C., Effect of cyclosporin A on alveolar bone homeostasis in a rat periodontitis model (2004) Journal of Periodontal Research, 39 (3), pp. 143-148. , DOI 10.1111/j.1600-0765.2004.00739.x
dc.descriptionSpolidorio, L.C., Spolidorio, D.M., Holzhausen, M., Nassar, P.O., Nassar, C.A., Effects of long-term cyclosporin therapy on gingiva of rats: Analysis by stereological and biochemical estimation (2005) Braz Oral Res, 19, pp. 112-118
dc.descriptionDolnikoff, M., Martin-Hidalgo, A., Machado, U.F., Lima, F.B., Herrera, E., Decreased lipolysis and enhanced glycerol and glucose utilization by adipose tissue prior to development of obesity in monosodium glutamate (MSG) treated-rats (2001) International Journal of Obesity, 25 (3), pp. 426-433. , DOI 10.1038/sj.ijo.0801517
dc.descriptionRibeiro, E.B., Oller Do Nascimento, C.M., Andrade, I.S., Hirata, A.E., Dolnikoff, M.S., Hormonal and metabolic adaptations to fasting in monosodium glutamate-obese rats (1997) Journal of Comparative Physiology - B Biochemical, Systemic, and Environmental Physiology, 167 (6), pp. 430-437. , DOI 10.1007/s003600050093
dc.descriptionNascimento Curi, C.M., Marmo, M.R., Egami, M., Ribeiro, E.B., Andrade, I.S., Dolnikoff, M.S., Effect of monosodium glutamate treatment during neonatal development on lipogenesis rate and lipoprotein lipase activity in adult rats (1991) Biochem Int, 24, pp. 927-935
dc.descriptionO'Neal, D.N., Hew, F.L., Best, J.D., Alford, F., The effect of 24 months recombinant human growth hormone (rh-GH) on LDL cholesterol, triglyceride-rich lipoproteins and apo [a] in hypopituitary adults previously treated with conventional replacement therapy (1999) Growth Hormone and IGF Research, 9 (3), pp. 165-173. , DOI 10.1054/ghir.1999.0102
dc.descriptionOida, K., Nakai, T., Hayashi, T., Plasma lipoproteins of monosodium glutamate-induced obese rats (1984) International Journal of Obesity, 8 (5), pp. 385-391
dc.descriptionBray, G.A., York, D.A., The Mona Lisa Hypothesis in the Time of Leptin (1998) Recent Progress in Hormone Research, 53, pp. 95-117
dc.descriptionEdvell, A., Lindstrom, P., Vagotomy in young obese hyperglycemic mice: Effects on syndrome development and islet proliferation (1998) Am J Physiol, 274, pp. 1034-E1039
dc.descriptionMacHo, L., Fickova, M., Jezova, Zorad, S., Late effects of postnatal administration of monosodium glutamate on insulin action in adult rats (2000) Physiol Res, 49 (SUPPL. 1), pp. 79-S85
dc.descriptionEckel, R.H., Insulin resistance: An adaptation for weight maintenance (1992) Lancet, 340, pp. 1452-1453
dc.descriptionSaad, R., Gungor, N., Arslanian, S.A., Progression from normal glucose tolerance to type 2 diabetes in a young girl: Longitudinal changes in insulin sensitivity and secretion assessed by the clamp technique and surrogate estimates (2005) Pediatric Diabetes, 6 (2), pp. 95-99. , DOI 10.1111/j.1399-543X.2005.00097.x
dc.descriptionThomas, T., Gori, F., Khosla, S., Jensen, M.D., Burguera, B., Riggs, B.L., Leptin acts on human marrow stromal cells to enhance differentiation to osteoblasts and to inhibit differentiation to adipocytes (1999) Endocrinology, 140 (4), pp. 1630-1638
dc.descriptionCornish, J., Callon, K.E., Bava, U., Lin, C., Naot, D., Hill, B.L., Grey, A.B., Reid, I.R., Leptin directly regulates bone cell function in vitro and reduces bone fragility in vivo (2002) Journal of Endocrinology, 175 (2), pp. 405-415. , DOI 10.1677/joe.0.1750405
dc.descriptionElefteriou, F., Ahn, J.D., Takeda, S., Starbuck, M., Yang, X., Liu, X., Kondo, H., Karsenty, G., Leptin regulation of bone resorption by the sympathetic nervous system and CART (2005) Nature, 434 (7032), pp. 514-520. , DOI 10.1038/nature03398
dc.descriptionRitchie, C.S., Obesity and periodontal disease (2007) Periodontology 2000, 44, pp. 154-163
dc.descriptionPage, R.C., The role of inclammatory mediators in the pathogenesis of periodontal disease (1991) J Periodontal Res, 26, pp. 230-242
dc.descriptionReichardt, H.M., Schutz, G., Glucocorticoid signalling - Multiple variations of a common theme (1998) Molecular and Cellular Endocrinology, 146 (1-2), pp. 1-6. , DOI 10.1016/S0303-7207(98)00208-1, PII S0303720798002081
dc.descriptionSterman Dolnikoff, M., Kater, C.E., Egami, M., Senna De Andrade, I., Marmo, M.R., Neonatal treatment with monosodium glutamate increases plasma corticosterone in the rat (1988) Neuroendocrinology, 48 (6), pp. 645-649
dc.descriptionVoltera, A.F., Cesaretti, M.L., Ginoza, M., Kohlmann, Jr.O., Effects of neuroendocrine obesity induction on systemic hemodynamics and left ventricular function of normotensive rats (2008) Arq Bras Endocrinol Metabol, 52, pp. 47-54
dc.languageen
dc.publisher
dc.relationArchives of Oral Biology
dc.rightsfechado
dc.sourceScopus
dc.titleDecreased Tnf-α Gene Expression In Periodontal Ligature In Msg-obese Rats: A Possible Protective Effect Of Hypothalamic Obesity Against Periodontal Disease?
dc.typeArtículos de revistas


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