Changes of peroxisomal fatty acid metabolism during cold acclimatization in hibernating jerboa (Jaculus orientalis)

Biochimie. 2003 Jul;85(7):707-14. doi: 10.1016/s0300-9084(03)00117-2.

Abstract

Jerboa (Jaculus orientalis) is a deep hibernator originating from sub-desert highlands and represents an excellent model to help to understand the incidence of seasonal variations of food intake and of body as well as environmental temperatures on lipid metabolism. In jerboa, hibernation processes are characterized by changes in the size of mitochondria, the number of peroxisomes in liver and in the expression of enzymes linked to fatty acid metabolism. In liver and kidney, cold acclimatization shows an opposite effect on the activities of the mitochondrial acyl-CoA dehydrogenase (-50%) and the peroxisomal acyl-CoA oxidase (AOX) (+50%), while in brown and white adipose tissues, both activities are decreased down to 85%. These enzymes activities are subject to a strong induction in brown and in white adipose tissue (3.4- to 7.5-fold, respectively) during the hibernation period which is characterized by a low body temperature (around 10 degrees C) and by starvation. Expression level of AOX mRNA and protein are increased during both pre-hibernation and hibernation periods. Unexpectedly, treatment with ciprofibrate, a hypolipemic agent, deeply affects lipolysis in brown adipose tissue by increasing acyl-CoA dehydrogenase activity (3.4-fold), both AOX activity and mRNA levels (2.8- and 3.8-fold, respectively) during pre-hibernation. Therefore, during pre-hibernation acclimatization, there is a negative regulation of fatty acid degradation allowing to accumulate a lipid stock which is later degraded during the hibernation period (starvation) due to a positive regulation of enzymes providing the required energy for animal survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acclimatization / physiology*
  • Acyl-CoA Oxidase / genetics
  • Acyl-CoA Oxidase / metabolism
  • Animals
  • Body Temperature Regulation / physiology
  • Cold Temperature*
  • Enzyme Activation
  • Fatty Acids / metabolism*
  • Hibernation*
  • Liver / cytology
  • Liver / enzymology
  • Liver / ultrastructure
  • Male
  • Mitochondria / enzymology
  • Peroxisomes / metabolism*
  • Peroxisomes / ultrastructure
  • RNA, Messenger / genetics
  • Rodentia / metabolism
  • Rodentia / physiology*

Substances

  • Fatty Acids
  • RNA, Messenger
  • Acyl-CoA Oxidase