Literature DB >> 3170826

Lipid synthesis and deposition by adult Richardson's ground squirrels in the natural environment.

G L Bintz1.   

Abstract

Adult male Richardson's ground squirrels, Spermophilus richardsonii, were estimated to have emerged from hibernation in late February to early March, and adult females in mid to late March. Half of the females trapped in late March were not pregnant, as against 10% after that time. In late March males and all females had similar WAT (white adipose tissue) deposits. Between late March and early June, WAT deposits in males increased from 14 g to 64 g (a rate of 5.6 g per week). In non-parous females WAT deposits increased from 13 g to 48 g from late March to late May (4.2 g per week). Fat deposits decreased during lactation but thereafter increased from 8 g to 29 g (a rate of 6.0 g per week) between early May and early June. In males the rate of fatty acid synthesis in BAT (brown adipose tissue), liver and WAT did not change from late March to late May, and rates in the corresponding tissues of non-pregnant females were similar to those in males. Fatty acid synthesis decreased during late pregnancy and lactation. After lactation, the rate of fatty acid synthesis in all tissues increased to that in males and non-pregnant females. Males initiated fattening 5-7 weeks earlier than females. It is concluded that compared with adult males, the later immergence of adult female Richardson's ground squirrels into hibernation is due primarily to later initiation of fattening and less to differences in rate of lipid synthesis after the reproductive period. Rates of fatty acid synthesis in liver and BAT were several times greater than that in WAT. The former tissues may contribute fatty acids for prehibernatory fattening.

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Year:  1988        PMID: 3170826     DOI: 10.1007/bf01075833

Source DB:  PubMed          Journal:  J Comp Physiol B        ISSN: 0174-1578            Impact factor:   2.200


  9 in total

1.  Measurement of rates of lipogenesis with deuterated and tritiated water.

Authors:  J M Lowenstein; H Brunengraber; M Wadke
Journal:  Methods Enzymol       Date:  1975       Impact factor: 1.600

2.  The energetics of fat deposition during growth.

Authors:  A J van Es
Journal:  Nutr Metab       Date:  1977       Impact factor: 4.169

3.  Endocrine control of fat mobilization in the isolated fat cells of cold-exposed rats.

Authors:  D G Therriault; R W Hubbard; D B Mellin
Journal:  Lipids       Date:  1969-11       Impact factor: 1.880

4.  Brown adipose tissue thermogenesis is 'suppressed' during lactation in mice.

Authors:  P Trayhurn; J B Douglas; M M McGuckin
Journal:  Nature       Date:  1982-07-01       Impact factor: 49.962

5.  Measurement of rates of cholesterol synthesis using tritiated water.

Authors:  J M Dietschy; D K Spady
Journal:  J Lipid Res       Date:  1984-12-15       Impact factor: 5.922

6.  Alterations in the rate of lipogenesis in vivo in maternal liver and adipose tissue on premature weaning of lactating rats: a possible regulatory role of prolactin.

Authors:  L Agius; A M Robinson; J R Girard; D H Williamson
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

7.  Changes in brown adipose tissue lipoprotein lipase activity and lipogenesis rate during pregnancy and lactation in the rat.

Authors:  F Villarroya; T Mampel
Journal:  Biochem Int       Date:  1986-09

8.  Energy balance and brown adipose tissue thermogenesis during pregnancy in Syrian hamsters.

Authors:  G N Wade; G Jennings; P Trayhurn
Journal:  Am J Physiol       Date:  1986-05

9.  Fatty acid synthesis in brown adipose tissue in relation to whole body synthesis in the cold-acclimated golden hamster (Mesocricetus auratus).

Authors:  P Trayhurn
Journal:  Biochim Biophys Acta       Date:  1980-10-06
  9 in total

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