Nigrostriatal and mesolimbic dopaminergic activities were modified throughout the ovarian cycle of female rats

J Neural Transm Gen Sect. 1991;85(3):223-9. doi: 10.1007/BF01244947.

Abstract

In this work, we have studied the changes in the functional state of nigrostriatal (NSDA) and mesolimbic (MLDA) dopaminergic neurons during the estrous cycle of the female rat. The activity of tyrosine hydroxylase (TH), the turnover rate (Kt) after inhibition of dopamine (DA) synthesis and the ratio between the contents of this amine and its metabolite, L-3,4 dihydroxyphenylacetic acid (DOPAC), were used as indices of neuronal activity. The neuronal activity of NSDA neurons rose during estrous and declined during proestrous, as reflected by the values of Kt and DOPAC/DA ratio measured during both phases. Interestingly, the course of variations in striatal TH activity was similar, although retarded in relation to the changes in neuronal activity. Thus, TH activity was high during diestrous, whereas it was low during estrous. The activity of MLDA neurons was reduced during proestrous. This can be concluded from the decreased Kt and DOPAC/DA ratio measured in this phase and it was accompanied by a low TH activity. Thereupon, both Kt and TH activity increased during estrous. These results indicate the existence of physiological changes in the functional state of both dopaminergic systems during the ovarian cycle, which are partially different for each neuronal pathway. This supports the existence of a specific regulation, and not indiscriminate effects, by the hormones involved in this cycle, mainly estradiol and progesterone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3,4-Dihydroxyphenylacetic Acid / metabolism
  • Animals
  • Dopamine / metabolism
  • Dopamine / physiology*
  • Estradiol / pharmacology
  • Estrus / physiology*
  • Female
  • Limbic System / physiology*
  • Progesterone / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Substantia Nigra / physiology*
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • 3,4-Dihydroxyphenylacetic Acid
  • Progesterone
  • Estradiol
  • Tyrosine 3-Monooxygenase
  • Dopamine