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1º ARTIGO NOTA CIENTÍFICA

2º ARTIGO – ARTIGO ORIGINAL

7. CONSIDERAÇÕES FINAIS E PERSPECTIVAS

Diante do exposto foi claro que a dieta hipoproteica oferecida durante gestação e lactação impõe mudanças no organismo materno desde o nível de consumo dietético até alterações fisio-metabólicas visivelmente quando se estende pela lactação. Porém, no organismo materno, os dados não nos permitem inferir se estes agravos observados são permanentes ou transitórios, e, se temporários, qual o período de reversão dessas alterações.

Na prole, os resultados mostraram que a manutenção da dieta hipoproteica após o desmame diminui o peso e o comprimento do animal, porém, percentualmente, não afeta este crescimento. Por outro lado, os animais “recuperados” se igualam aos animais controle, confirmando a presença do catch-up. Foram observados vários parâmetros semelhantes entre os grupos controle e “recuperado”, que pode ser decorrente da jovem idade em que os animais foram avaliados. A literatura mostra possíveis consequências metabólicas após uma recuperação nutricional em animais desnutridos na vida perinatal. Contudo, estas desordens surgem tardiamente em idades igual ou superior a 180 dias, momento semelhante a um adulto de meia idade. Vale salientar que os animais que mantiveram a dieta hipoproteica apresentam uma maior tolerância à glicose, assim como um menor teor de gordura visceral nos incitando a refletir sobre diversas repercussões que possam advir a este organismo em longo prazo.

Desta forma, os resultados obtidos com a continuidade da dieta hipoproteica até a idade estudada nos permitem concluir a existência de um estado de resposta preditiva- adaptativa nos animais LPP que pode sofrer interferências com o avançar da idade, sendo necessário estudos posteriores para confirmar a permanência ou não deste estado.

Ao término deste trabalho foram levantadas novas hipóteses que levam a continuação deste e de mais estudos nesta temática:

 Estudar os efeitos sobre o metabolismo materno e as consequências fisio-metabólicas na prole de mães submetidas à desnutrição proteica desde o período pré-gestacional.  Estudar os efeitos da desnutrição proteica em um grupo de animais recém-

desmamados. Desta forma, poderia se estabelecer quais alterações fisio-metabólicas são restritas ao período perinatal;

 Estudar a manutenção da dieta materna, inclusive a hipoproteica, por um período além dos 90 dias. Assim, na idade adulta, os animais poderiam, ou não, apresentam alterações fisio-metabólicas decorrentes do insulto no período perinatal;

 Estudar outras estruturas corporais, como por exemplo, o hipotálamo dos animais, que poderiam trazer um respaldo aos resultados encontrados;

 Realizar o teste de sensibilidade à insulina ao final do experimento, que, associado com o teste de tolerância oral à glicose, poderia demonstrar com mais clareza até que ponto os animais apresentam uma alteração a nível deste hormônio.

 Realizar nos grupos teste de tolerância à glicose por via intraperitoneal e análise histológica de segmentos do trato gastrointestinal.

REFERÊNCIAS

ALVES AP, DÂMASO AR, DAL PAI V. Efeito da desnutrição protéica pré e pós-natal sobre a morfologia, a diferenciação e o metabolismo do tecido muscular estriado esquelético em ratos. Jornal de Pediatria - Vol. 84, Nº 3, 2008.

ARAYA JA, BARRIGA CP. Efecto de la preñez y La lactancia en el estado nutricional de los ácidos grasos esenciales, en la rata. Rev Med Chile. 124:923-7; 1996.

ARMITAGE JA, et al, 2005 J Physiol, pp3-8. 2005.

BADONNEL K, LACROIX MC, MONNERIE R, DURIEUX D, CAILLOL M, BALY C. Chronic restricted access to food leading to undernutrition affects rat neuroendocrine status and olfactory-driven behaviors. Horm Behav. Jul;62(2):120-7. 2012.

BARKER DJP. The malnourished baby and infant. British Medical Bulletin. 60. 69–88. 2001.

BARKER, D.J. The origins of the developmental origins theory. J Intern Med. 261(5):412-7, 2007.

BARKER DJP: In útero programming of cardiovascular disease. Theriogen, 53: 555-574. 2000.

BARKER, D.J. Early growth and cardiovascular disease. Arch Dis Child. Apr v. 80, n.4, p. 305-7, 1999

BARNES, R.H., CUNNOLD, S.R., ZIMMERMANN, R.R., et al. Influence of Nutritional Deprivations in Early Life on Learning Behavior of Rats as Measured by Performance in a Water Maze. J. Nutrition. 89: '66, 1966.

BATESON P, MARTIN PC. Design for a Life: How Behaviour Develops. London: Cape; 1999.

BAYOL, S. JONES, D. ; GOLDSPINK, G. ; STICKLAND, N.C. The influence of undernutrition during gestation on skeletal muscle cellularity and on the expression of genes that control muscle growth. Br J Nutr, v. 91, n. 3, p. 331-339, 2004.

BEDI, K. S.; BIRZGALIS, A.R. ; MAHON, M. ; SMART, J.L. ; WAREHAM, A.C. Early life undernutrition in rats. 1. Quantitative histology of skeletal muscles from underfed young and refed adult animals. Br J Nutr, v. 47, n. 3, p. 417-431, 1982.

BELLINGER, L., C. LILLEY, AND S.C. LANGLEY-EVANS. Prenatal exposure to a maternal low-protein diet programmes a preference for high-fat foods in the young adult rat.

Br J Nutr, 92(3): p. 513-20; 2004.

BELLO, A.C.D., RIUL, T.R., DE OLIVEIRA, L.M. Desnutrição e estresse na gestação: medidas comportamentais das mães e dos filhotes durante a lactação. Temas em Psicologia

BENNIS-TALEB N, REMACLE C, HOET JJ, REUSENS B; A low-protein isocaloric diet during gestation affects brain development and alters permanently cerebral cortex blood vessels in rat offspring. J Nutr. Aug;129(8):1613-9. 1999.

BERNEY DM, DESAI M, PALMER DJ, GREENWALD S, BROWN A, HALES CN, BERRY CL. The effects of maternal protein deprivation on the fetal rat pancreas: major structural changes and their recuperation. J Pathol. Sep;183(1):109-15; 1997.

BERTRAM, D.; BARRES, C.; CHENG, Y.;JULIEN, C. Norepinephrine reuptake, baroreflex dynamics, and arterial pressure variability in rats. Am J Physiol Regul.Integr.Comp

Physiol, v. 279, n. 4, p. R1257-R1267, 2000.

BLACK, R.E. Micronutrients in pregnancy. British Journal of Nutrition, v.85, n.2, p.193- 197, 2001.

BLUNDELL J. Pharmacological approaches to appetite suppression. Trends Pharmacol Sci. 12(4): 147-57; 1991.

BOYD, R.D., KENSINGER, R.S., HARRELL, R.J., BAUMAN, D.E. Nutrientuptake and endocrine regulation of milk synthesis by mammarytissue of lactating sows. J AnimSci 73(Suppl 2):36–56; 1995.

BRASIL, F.B., FARIA, T.S., SAMPAIO, F.J.B., et al. The Effect of Maternal Malnutrition During Lactation on the Endometrial ERα Expression, Collagen Type, and Blood Vessels in the Rats Offspring at Puberty. The Anatomical Record, 293(1): 162–170, 2010.

BROWN, P.I., BRASEL, J.A. “Endocrinechanges in themalnourishedchild”. In: SUSKIND,R. M. & LEWINTER-SUSKIND, L. (eds.). The malnourished child. New York, NestléNutritionWorshop Series, v. 19, Nestec Ltd., Vevey/Raven Press Ltd., 1990.

BURDGE GC, HANSON MA, SLATER-JEFFERIES JL, LILLYCROP KA. Epigenetic regulation of transcription: a mechanism for inducing variations in phenotype (fetal programming) by differences in nutrition during early life? Br J Nutr. 97(6):1036-46; 2007. CALDWELL, D.F., CHURCHILL, J.A. Learning ability in progeny of rats administered a protein-deficient diet during the second half of gestation. Neurology, v. 17, p. 95-9, 1967. CAMM EJ, MARTIN-GRONERT MS, WRIGHT NL, HANSELL JA, OZANNE SE, GIUSSANI DA. Prenatal hypoxia independent of undernutrition promotes molecular markers of insulin resistance in adult offspring. FASEB J. 2010.

CAMPOS SD, MADI K. Desnutrição experimental: resultados anátomo-patológicos e bioquímicos da administração de dietas hipoprotéicas a ratos albinos jovens. Mem Inst

Oswaldo Cruz. 73(3):153-81. 1975.

COTTRELL EC, OZANNE SE. Early life programming of obesity and metabolic disease.

COUPE B, GRIT I, DARMAUN D, PARNET P. The timing of “catch-up growth” affects metabolism and appetite regulation in male rats born with intrauterine growth restriction. Am

J Physiol Regul Integr Comp Physiol. 297(3):R813-24. 2009.

CURTISS, C. Effects of a low protein intake on the pregnant rat. Metabolism. 2(4): 344-58. 1953.

DE SANTANA MUNIZ, G., DA SILVA, A. M. A., CAVALCANTE, T. C. F., DA SILVA, F., KARLA, A., FERRAZ, K. M., & DO NASCIMENTO, E. Early physical activity minimizes the adverse effects of a low-energy diet on growth and development parameters.

Nutritional neuroscience, 16(3), 113-124. 2013.

DE SOUZA, A.S., PACHECO, L.C., CASTRO, O.S., et al. Brain fatty acid profiles and spatial learning in malnourished rats: effects of nutritional intervention Volume 11 Issue 3 (01 June), pp. 119-127, 2008.

DE SOUZA AS, PACHECO LC, CASTRO PS, DO CARMO MGT. Influência da desnutrição promovida pela dieta básica regional sobre o perfil de ácidos graxos do leite materno, o crescimento e o desenvolvimento de ratos jovens. Rev. Nutr., Campinas, 22(4):467-481, jul./ago., 2009.

DE SOUZA, S.L., DA SILVA, A.I., DA SILVA, M.C., et al. Efeito da Desnutrição Materna sobre o Comportamento Alimentar em Ratos Neonatos. Neurobiologia. 72 (4) out./dez, 2009. ELIA, M. Hunger disease. Clin Nutr., v. 19, n. 6, p. 379-386, 2000.

FALCAO-TEBAS F, BENTO-SANTOS A, FIDALGO MA, DE ALMEIDA MB, DOS SANTOS JA, LOPES DE SOUZA S, et al. Maternal low-protein diet-induced delayed reflex ontogeny is attenuated by moderate physical training during gestation in rats. Br J Nutr. 107(3):372-7. 2012.

FAO. Statistical Yearbook. http://www.fao.org/publications/en/. 2013.

FERNANDES RM, et al. Maternal malnutrition during lactation reduces skull growth in weaned rat pups: Experimental and morphometric investigation. Anat Sci Int, 83: 123–130. 2008.

FERNANDES RMP, et al. Effect of protein and energy restricted diet during lactation leads to persistent morphological changes on tibia growth in the weaned pups. Int. J. Morphol, 25(3): 565-571. 2007.

FORSDAHL, A. Are poor living conditions in childhood and adolescence an important risk factor for arteriosclerotic heart disease? Br J Prev Soc Med. 31(2):91-5, 1977.

FRIEDEWALD WT, LEVY RL, FREDRICKSON DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma without the use of preparative

ultracentrifuge. Clin Chem. 18: 499-502. 1972.

GEURSEN A, CARNE A, GRIGOR MR. Protein Synthesis in Mammary Acini Isolated from Lactating Rats: Effect of Maternal Diet. J. Nutr. 117: 769-775, 1987.

GLUCKMAN P, HANSON M. The Fetal Matrix: Evolution, Development and Disease. Cambridge: Cambridge University Press, 2004.

GLUCKMAN PD, HANSON MA, SPENCER HG. Predictive adaptive responses and human evolution. Trends Ecol Evol;20:527–33. 2005.

GLUCKMAN, P.D., HANSON, M.A. Developmental plasticity and human disease: research directions. J Intern Med. 261:461-71, 2007.

GLUCKMAN PD, HANSON MA, BEEDLE AS. Early life events and their consequences for later disease: a life history and evolutionary perspective. Am J Hum Biol;19:1–19. 2007. GOLAN, D. E. et al. Princípios de Farmacologia: A Base Fisiopatológica da

Farmacoterapia. 2 edição. Rio de Janeiro: Guanabara Koogan, 2009.

GRIMBLE, R.F., MANSARAY, Y.K. Effects in rats of dietary protein inadequacy on lactose production, milk volume and components of the lactose synthetase complex (EC 2.4.1.22).

Ann Nutr Metab, 31(3): p. 179-84; 1987.

GUTHRIE, H.A., PICCIANO, M.F. Human nutrition.Saint Louis: MOSBY. 654p, 1995. HALES, C.N., BARKER, D.J. Type 2 (non-insulindependent) diabetes mellitus: the thrifty phenotype hypothesis. Diabetologia. 35(7):595-601, 1992.

HERBERT DC: Morphology of the mammotrophs and gonadotrophs in the anterior pituitary gland of rats with protein-calorie malnutrition. Am J Anat, 158: 521–531. 1980.

HERRERA, E. Implications of dietary fatty acids during pregnancy on placental, fetal and postnatal development - a review. Placenta. Apr;23 Suppl A:S9-19, 2002.

HERRERA, E; RAMOS ÁLVAREZ, M. PILAR. Papel deltejido adiposo, sensibilidad insulínica e ingesta lipídica enlagestación y suimplicaciónenelriesgo de padecer diabetes

enlaedad adulta. Monografías de la Real Academia Nacional de Farmacia, 2009.

HEYWOOD, W.E., MIAN, N., MILLA, P.J., Keith J. LINDLEY, K.J. Programming of defective rat pancreatic β-cell function in offspring from mothers fed a low-protein diet during gestation and the suckling periods Wendy E. HEYWOOD, Clinical Science 107, 37– 45; 2004.

HOPPE, C.C., EVANS, R.G., BERTRAM, J.F., MORITZ, K.M. Effects of dietary protein restriction on nephron number in the mouse. Am J Physiol Regul Integr Comp Physiol. v.292, n.5, p.R1768-74, 2007.

JANSSON, N., PETTERSSON, J., HAAFIZ, A., ERICSSON, A., PALMBERG, I., TRANBERG, M., et al. Down-regulation of placental transport of aminoacids precedes the development of intrauterine growth restriction in rats fed a low protein diet. J Physiol 576.3 pp 935–946, 2006.

JEAN FAUCHER C, BERGER M, TURCKHEIM M, VEYSSIERE G, JEAN C: Effect of pre weaning undernutrition on testicular development in male mice. Int J Androl, 5: 627– 635. 1982.

JOBGEN, W.S., FRIED, S.K., FU, W.J., MEININGER, C.J., WU, G. Regulatoryrole for thearginine-nitric oxide pathway in metabolismofenergysubstrates. J Nutr Biochem 17:571– 588; 2006.

KARL, P.I., ALPY, K.L., FISHER, S.E. Insulin-like growth factor-1 stimulates amino acid uptake by the cultured human placental trophoblast. J Cell Physiol 165, 83–88. Amino acid transport by the cultured human placental trophoblast: effect of insulin on AIB transport. Am

J Physiol 262, C834–C839; 1992.

KHAN, I. Predictive Adaptive Responses to Maternal High-Fat Diet Prevent Endothelial Dysfunction but Not Hypertension in Adult Rat Offspring. Circulation. 110:1097-1102. 2004.

KIM, S.W., HURLEY, W.L., HAN, I.K., EASTER, R.A. Growth of nursing pigs related to the characteristics of nursed mammary glands. J AnimSci 78:1313–1318; 2000.

KING, J.C., WEININGER, J. Embarazo y lactancia. Washington DC: Organización

Panamericana de laSalud. p.362-368. (OPAS – PublicaciónCientifica, 532), 1991.

KRÓL E, KREJPCIO Z, CHMURZYNSKA A. Folic Acid and Protein Content in Maternal Diet and Postnatal High-Fat Feeding Affect the Tissue Levels of Iron, Zinc, and Copper in the Rat. Biol Trace Elem Res. 144:885–893. 2011.

KUM KUM, S. BHASIN, ATILA VAN NAS, LISA J. MARTIN, RICHARD C. DAVIS, SHERIN U. DEVASKAR, ANDALDONS J. LUSIS. Maternal Low-Protein Diet or Hypercholesterolemia Reduces Circulating Essential Amino Acids and Leads to Intrauterine Growth Restriction. Diabetes, vol. 58, march 2009.

KWONG WY, WILD AE, ROBERTS P, WILLIS AC, FLEMING TP. Maternal undernutrition during the preimplantation period of rat development causes blastocyst abnormalities and programming of postnatal hypertension. Development. 127, 4195-4202. 2000.

LESAGE J, DUFOURNY L, LABORIE C, BERNET F, BLONDEAU B, AVRIL I, BRÉANT B, DUPOUY J Perinatal malnutrition programs sympathoadrenal and hypothalamic-pituitary-adrenal axis responsiveness to restraint stress in adult male rats. J

Neuroendocrinol. Feb;14(2):135-43. 2002.

LING WANG RUO-JUN XU. The effects of perinatal protein malnutrition on spatiall earning and memory behavior and brain-derived neurotrophic factor concentration in the brain tissue in young rats. Asia Pac J Clin Nutr;16 (Suppl 1):467-472. 2007.

LINS MC, et al. Effects of maternal leptin treatment during lactation on the body weight and leptin resistance of adult offspring. Regul Pept, 127: 197–202. 2005.

LOPES DE SOUZA S, et al. Perinatal protein restriction reduces the inhibitory action of serotonin on food intake. Eur J Neurosci, 27(6): p. 1400-8. 2008.

LUCAS, S. R.; COSTA SILVA, V. L.; MIRAGLIA, S. M.;ZALADEK, G. F. Functional and morphometric evaluation of offspring kidney after intrauterine undernutrition.

Pediatr.Nephrol., v. 11, n. 6, p. 719-723, 1997.

MAZETI CM, FURLAN MMDP. Crescimento e parâmetros reprodutivos de ratas Wistar, em restrição alimentar desde o nascimento. Acta Sci. Biol. Sci. Maringá, v. 30, n. 2, p. 197-204, 2008.

MCCRABB, G.J., EGAN, A.R., HOSKING, B.J. Maternal undernutrition during mid- pregnancy in sheep. Placental size and its relationship to calcium transfer during late pregnancy. Br J Nutr. Mar;65(2):157-68, 1991.

McGARRY JD. Banting lecture 2001: dysregulation of fatty acid metabolism in the etiology of type 2 diabetes. Diabetes. 51(1):7-18. 2002.

MELLO, M.A.R., CURY, L. Influence of protein-calorie malnutrition on reproductive performance Young and mature rats. Growth Development and aging, v. 53, p. 141-4. 1989. MELLOR DJ, MURRAY. Effects of long term undernutrition of the ewe on the growth rates of individual fetuses during late pregnancy. L. Res Vet Sci. Mar;32(2):177-80. 1982.

MERCER JG, SPEAKMAN JR. Hypothalamic neuropeptide mechanisms for regulating energy balance: from rodent models to human obesity. Neurosci Biobehav Rev. 25(2):101- 16. 2001.

MONTEIRO JS, GUEDES RCA, CASTRO RM, FILHO JEC Estimulação psicossocial e plasticidade cerebral em desnutridos. Rev. bras. saúde matern. infant., Recife, 2 (1): 15-22, jan. - abril, 2002.

MORGANE M, MILLER M, KEMPER T, et al. The effects of protein malnutrition on the developing nervous system in the rat. Neuroscience;2: 137-230. 1978.

MORGANE PJ, AUSTIN-LAFRANCE R, BRONZINO J, TONKISS J, DÍAZ-CINTRA S, CINTRA L, et al. Prenatal malnutrition and development of the brain. Neurosci Biobehav

Rev. 17(1):91-128. 1993.

MORTON GJ, CUMMINGS DE, BASKIN DG, BARSH GS, SCHWARTZ MW. Central nervous system control of food intake and body weight. Nature. 443(7109):289-95. 2006. MULAY, S. et al. Influence of protein deficiency on hormonal status and cytoplasmic glucocorticoid receptors maternal and fetal tissues. J.Endocrinol, v. 95, p. 49-58, 1982. NAISMITH DJ, RICHARDSON DP, PRITCHARD AE The utilization of protein and energy during lactation in the rat, with particular regard to the use of fat accumulated in pregnancy..

NAGASE H, NAKAJIMA A, SEKIHARA H, YORK DA, BRAY GA. Regulation of feeding behavior, gastric emptying, and sympathetic nerve activity to interscapular brown adipose tissue by galanin and enterostatin: the involvement of vagal-central nervous system interactions. J Gastroenterol. 37(Suppl 14):118-27. 2002.

NASCIMENTO, E., GUZMAN-QUEVEDO, O., DELACOURT, N., et al. Long-lasting effect of perinatal exposure to L-tryptophan on circadian clock of primary cell lines established from male offspring born from mothers fed on dietary protein restriction. PLoS

One. 8(2):e56231. 2013.

NASCIMENTO E, DE SANTANA MUNIZ G, DE SANTANA MUNIZ MG, ALEXANDRE LS, DA ROCHA LS, LEANDRO CG, CASTRO RM, BOLAÑOS-JIMENEZ F. Unlimited access to low-energy diet causes acute malnutrition in dams and alters biometric and biochemical parameters in offspring. Journal of Developmental Origins of Health and

Disease, p. 1-11. 2014.

NELSON, D.M., SMITH, S.D., FURESZ, T.C., SADOVSKY, Y., GANAPATHY, V., PARVIN, C.A. SMITH, C.H. Hypoxia reduces expression and function of system A amino acid transporters in cultured term human trophoblasts. Am J Physiol Cell Physiol. 284, C310–C315; 2003.

NUNES, Magda Lahorgue; BATISTA, Bianca Brum; MICHELI, Flávia and BATISTELLA, Vinicius. Efeitos da desnutrição precoce e reabilitação nutricional em ratos. J. Pediatr. (Rio J.) [online]. vol.78, n.1, pp. 39-44. ISSN 0021-7557. 2002.

NWUGA, V.C. Effect of severe kwashiorkor on intellectual development among Nigerian children. Am J Clin Nutr. Sep;30(9):1423-30, 1977.

OHISHI T, WANG L, AKANE H, SHIRAKI A, SATO A, UEMATSU M, SUZUKI K, MITSUMORI K, SHIBUTANI M. Adolescent hyperactivity of offspring after maternal protein restriction during the second half of gestation and lactation periods in rats. J. Toxicol.

Sci. Vol.37, No.2, 345-352, 2012.

OROZCO-SOLIS R, LOPES DE SOUZA S, BARBOSA MATOS RJ, GRIT I, LE BLOCH J, NGUYEN P, et al. Perinatal undernutrition-induced obesity is independent of the developmental programming of feeding. Physiol Behav. 96(3):481-92. 2009.

OROZCO-SOLIS R, MATOS RJ, GUZMAN QUEVEDO O, LOPES DE SOUZA S, BIHOUEE A, HOULGATTE R, et al. Nutritional programming in the rat is linked to longlasting changes in nutrient sensing and energy homeostasis in the hypothalamus. PLoS

One. 5(10):e13537. 2010.

OSUNTOKUN, B.O. The effects of malnutrition on the development of cognitive functions of the nervous system in childhood. Trop Geogr Med. Dec;24(4):311-26. Review, 1972. OZANNE, S.E., JENSEN, C.B., TINGEY, K.J., et al. Low birthweight is associated with specific changes in muscle insulin-signalling protein expression. Diabetologia. 48(3): 547-52, 2005.

OZANNE SE, OLSEN GS, HANSEN LL, TINGEY KJ, NAVE BT, WANG CL, et al. Early growth restriction leads to down regulation of protein kinase C zeta and insulin resistance in skeletal muscle. J Endocrinol. 177(2):235-41. 2003.

OZANNE, S. E. et al. Altered regulation of hepatic glucose output in the male offspring of protein-malnourished rat dams.Am J Physiol, v. 270, n. 1, p. E559-564, 1996;

OZANNE, S. E, HALES, C. N. The long-term consequences of intra-uterine protein malnutrition for glucose metabolism.Proc Nutr Soc, v. 58, n 3, p. 615-619, 1999;

OUMI, M.; MIYOSHI, M.; YAMAMOTO, T. The ultrastructure of skeletal and smooth muscle in experimental protein malnutrition in rats fed a low protein diet. Arch Histol Cytol, v. 63, n. 5, p. 451-457, 2000.

PARK, K. S. ; KIM, S.K. ; KIM, M.S. ; CHO, E.Y. ; LEE, J.H. ; LEE, K.U. ; PAK, Y.K. ; LEE, H.K. Fetal and early postnatal protein malnutrition cause long-term changes in rat liver and muscle mitochondria. J Nutr, v. 133, n. 10, p. 3085-3090, 2003.

PARRA MO, HERNANDEZ-BLAQUEZ FJ, SOUZA E SILVA RAP, SILVA JRMC, PEDUTO L. Reduction of liver mass due to malnutrition in rats. Correlation with emaciation of animals and size of organs not inserted in the portal system. São Paulo Med. 113(3): 903- 9. 1995.

PASSOS, M.C.F., RAMOS, C.F., TEIXEIRA, C.V., et al. Comportamento alimentar de ratos adultos submetidos à restrição protéica cujas mães sofreram desnutrição durante a lactação.

Rev. Nutr., Campinas. 14 (suplemento):7-11, 2001.

PASSOS, M.C.F., RAMOS, C.F., MOURA, E.G. Short and long term effects of malnutrition in rats during lactation on the body weight of offspring. Nut Res, 20: 1603-1612. 2000. PATRÍCIO FR, NÓBREGA FJ, TONETE SS. Desnutrição intra-uterina em diferentes períodos de gestação em ratas: estudo do intestino delgado proximal ao nascimento e durante a recuperação nutricional. Rev Paul Ped. 2:43-52. 1984.

PETRIK J, REUSENS B, ARANY E, REMACLE C, COELHO C, HOET JJ, et al. A low protein diet alters the balance of islet cell replication and apoptosis in the fetal and neonatal rat and is associated with a reduced pancreatic expression of insulin-like growth factor-II.

Endocrinology. 140(10):4861-73. 1999.

PICAREL-BLANCHOT F, ALVAREZ C, BAILBE D, PASCUAL-LEONE AM, PORTHA B. Changes in insulin action and insulin secretion in the rat after dietary restriction early in life: influence of food restriction versus low-protein food restriction. Metabolism 44, 1519– 1526. 1995.

PICCIANO MF. Pregnancy and lactation: physiological adjustments, nutritional requirements and the role of dietary supplements. J Nutr. 133(3): 1997-2002. 2003.

PINE , A.P., JESSOP, N.S., OLDHAM, J.D., Maternal protein reserves and their influence on lactational performance in rats. 3. The effects of dietary protein restriction and stage of lactation on milk composition. Br J Nutr, 72(6): p. 815-30, 1994.

PINE, A.P., JESSOP, N.S., ALLAN, G.F., OLDHAM, J.D. Maternal protein reserves and their influence on lactational performance in rats. 2. Effects of dietary protein restriction during gestation and lactation on tissue protein metabolism and Na+, K(+)-ATPase (EC 3.6.1.3) activity. Br J Nutr, 72(2): p. 181-97, 1994.

PLAGEMANN, Andreas et al. Hypothalamic galanin levels in weanling rats exposed to maternal low-protein diet. Nutrition Research, v. 20, n. 7, p. 977-983, 2000.

RAMOS, C.F., MARQUES, J.A., BABINSKI, M.A., et al. Maternal malnutrition during lactation reduces estradiol serum concentration, prostate growth and ERα expression in the weaned pups. Urol, 2005.

RASMUSSEN, K.M., WARMAN, N.L. Effect of maternal malnutrition during the reproductive cycle on growth and nutritional status of suckling rat pups. Am J Clin Nutr, 38(1): p. 77-83, 1983.

RASMUSSEN, K.M. Effects of under- and over nutrition on lactation on laboratory rats. J

Nutr. 128(Suppl.2):390S-3S. 1998.

RAVELLI, G.P., STEIN, Z.A., SUSSER, M.W. Obesity in young men after famine exposure in utero and early infancy. N Engl J Med. 295(7):349-53, 1976.

REYES-CASTRO LA, RODRIGUEZ JS, CHARCO R, BAUTISTA CJ, LARREA F, NATHANIELSZ PW, ZAMBRANO. Maternal protein restriction in the rat during pregnancy and/or lactation alters cognitive and anxiety behaviors of female offspring. E. Int J Dev

Neurosci. Feb;30(1):39-45. 2012.

RIUL, T.R., et al. Ethological analysis of motherpup interactions and other behavioral reactions in rats: effects of malnutrition and tactile stimulation of the pups. Braz J Med Biol

Res, 32(8): p. 975-83; 1999.

ROLO AP, PALMEIRA CM. Diabetes and mitochondrial function: role of hyperglycemia and oxidative stress. Toxicol Appl Pharmacol. 2006;

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