Alcohol
Volume 21, Issue 3 , Pages 195-200, July 2000

Ethanol intake during lactation:

I. Effects on dams' metabolism and pups' body weight gain

  • L.M Oyama

      Affiliations

    • Departamento de Fisiologia, Universidade Federal de São Paulo-EPM, São Paulo, SP 04023-060, Brazil
  • ,
  • R.C Couto

      Affiliations

    • Departamento de Ciências Fisiológicas, Universidade do Amazonas, Manaus, AM, 69007-000, Brazil
  • ,
  • G.E.C Couto

      Affiliations

    • Departamento de Desporto e Atividades Comunitárias, Universidade do Amazonas, Manaus, AM, 69007-000, Brazil
  • ,
  • A.R Dâmaso

      Affiliations

    • Departamento de Educação Fı́sica e Motricidade Humana, Universidade Federal de São Carlos, São Carlos, SP 13565-535, Brazil
  • ,
  • C.M Oller do Nascimento

      Affiliations

    • Departamento de Fisiologia, Universidade Federal de São Paulo-EPM, São Paulo, SP 04023-060, Brazil
    • Corresponding Author InformationCorresponding author. Departamento de Fisiologia — Disciplina de Neurofisiologia e Fisiologia Endócrina, Rua Botucatu, 862, 2° andar-Edifı́cio de Ciências Biomédicas, Vila Clementino — São Paulo, SP 04023-060, Brazil. Tel.: +55-11-576-4527; fax: +55-11-570-7675

Received 28 July 1999; received in revised form 29 November 1999; accepted 13 December 1999.

Abstract 

Wistar lactating rats (8 pups per dam) had free access to either tap water (control group, C) or one of three concentrations of ethanol (E) in the drinking water: 5% (E5), 10% (E10), and 20% (E20). All animals received normal rat chow ad libitum and were killed on day 12 of lactation. Intake of both 10% and 20% ethanol solutions decreased food intake, dams' body weight, and pups' body weight gain as compared with findings in the C group. The relative weights (g/100g b.w.) of the mammary glands (MG) and of the parametrial white adipose tissue depot were decreased only in E20 as compared with findings in the C group. Protein and lipid content of these tissues were not altered in any of the ethanol groups. In comparison with the C group, the lipogenesis rate was increased in the MG (135.6%) and liver (120.2%) in E5 and the MG (58.1%) and parametrial white adipose tissue depot (147.0%) in E20. No modifications in lipogenesis rate were noted in E10. The malic enzyme activity was decreased in the MG in E10 (25.3%) and E20 (26.4%) and in the liver in E20 (45.7%). In E5, however, it was increased in the liver (23.9%). The activity of ATP-citrate lyase in the liver was decreased in E20 (56.7%), while it was increased by 37.5% in E5 and 34.2% in E10. Blood glucose concentration of dams was not affected by ethanol ingestion. However, plasma triacylglycerol concentration was higher in E10 (17.9%) and E20 (13.3%) than in the C group, and plasma protein was lower in E20 (15.7%) than in C. We concluded that alcohol intake during lactation increased the MG lipogenesis rate; although at the highest dose, this metabolic alteration was not enough to allow normal pups' growth. However, the low dose of ethanol (5%), despite having altered dams' metabolism, did not affect pups' body weight gain.

Keywords:  Alcohol, Lactation, Mammary gland, Liver, Lipogenesis, Rat, ATP-citrate lyase, Malic enzyme

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PII: S0741-8329(00)00073-2

Alcohol
Volume 21, Issue 3 , Pages 195-200, July 2000