Studies of prostatic cytosol protein kinases of the aging ACI rat

Said A. Goueli, Michael J. Wilson, Alan T. Davis, Khalil Ahmed

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8 Scopus citations


Changes in prostatic cytosolic cyclic AMP (cAMP)-dependent and -independent protein kinases associated with aging in ACI rats were determined. A decrease in prostatic weight and tissue protein content (but not DNA) with age was noted. The cytosolic cAMP-dependent protein kinase was present predominantly as the type II isozyme. Total content of this enzyme per prostate declined by 37% in 12-month-old rats but remained relatively stable thereafer. However, the activity ratio (+cAMP/-cAMP) increased with aging, indicating an elevation in the amount of the holoenzyme or a decrease in the amount of the free catalytic subunit. Concomitantly the specific activity (activity/unit protein in the cytosol) of this enzyme was found to be increased; this is most likely due to the loss of bulk proteins in the cytosol, and may indicate a slower loss of this enzyme protein in relation to other cytosolic proteins. By comparison, the cAMP-independent protein kinase demonstrated a marked and progressive decline in amount as well as in specific activity with aging, e.g. 80-90% decline at 12 months of age. The above changes in these enzymes did not appear to be due to low circulating androgen in the animals, since they were not reversed on administration of 3.0 mg of testosterone propionate per rat daily for four consecutive days. It is therefore suggested that the above-described changes in prostatic cytosolic protein kinases are primarily associated with cellular senescence in this organ.

Original languageEnglish (US)
Pages (from-to)371-382
Number of pages12
JournalMechanisms of Ageing and Development
Issue number3-4
StatePublished - Nov 12 1983
Externally publishedYes

Bibliographical note

Funding Information:
Miss Kathy Ferkul, Miss Amy Setzer and Mr. Roger Salem provided skilled technical assistance during the course of this work. The rats used in this investigation were received from Harlan Industries, Inc., through the auspices of the Chemical Research Resources Program, a function of the Division of Cancer Cause and Prevention, N.C.I., Bethesda, MD. In this regard, we also acknowledge with gratitude the help of Dr. David G. Longfellow. This ffork was supported in part by research grant no. CA 15062 awarded by the National Cancer Institute, D.H.H.S., and by the Medical Research Fund of the Veterans Administration.


  • 5-α-Dihydrotestosterone
  • Aging
  • Cytosolic cAMP-dependent protein kinases
  • Cytosolic cAMP-independent protein kinases
  • Prostate


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