. Testosterone prevents the heat shock-induced overactivation of glycogen synthase kinase-3 beta but not of cyclin-dependent kinase 5 and c-Jun NH2-terminal kinase and concomitantly abolishes hyperphosphorylation of tau: implications for Alzheimer's disease. Proc Natl Acad Sci U S A. 2002 Feb 5;99(3):1140-5. PubMed.


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  1. This research group uses hyperthermia to induce a form of generalized stress that this group calls "heat shock" in its reports, but it is my understanding that this group is alone in application of this nomenclature. Exposure of cultured cells (not living animals) is a more accepted protocol for inducing "heat shock" and studying "heat shock proteins", many of which act as chaperones, as a means of defense against the protein denaturation caused by the elevated temperature. Exposure of living animals to a heated environment is most typically used to model the human febrile state (i.e., fever). Elevation of body temperature has a myriad of effects, both systemic and neurological. In general, metabolism is accelerated, at least within a limited range. At very supraphysiological levels, proteins unfold and denature, and cells die.

    This report exemplifies an important stage in the study of the molecular pathology of tau, i.e., moving into live animal models. Rodent tau is not identical to its human counterpart, and rodent tau is not competent to form neurofibrillary tangles. Transgenic mice bearing human tau with the mutation that causes familial frontotemporal dementia have recently been developed by Mike Hutton and his colleagues at Mayo Jacksonville. The neurons in the brains of these transgenic mice, when exposed to a well-documented insult such as amyloid peptides, are now competent to assume a conformation highly similar to neurofibrillary tangles (Lewis et al. 2001, Gotz et al. 2001). This rodent will now be a valuable tool for evaluating in vivo the role in tangle formation for various protein kinases and phosphatases as well as small molecules (e.g., glycosaminoglycans). In light of the rat "heat shock" data, it would be very interesting to expose a tangle-competent mouse to hyperthermia and assay to determine whether this insult modifies the intensity or time course of tangle formation.
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    . Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP. Science. 2001 Aug 24;293(5534):1487-91. PubMed.

    . Formation of neurofibrillary tangles in P301l tau transgenic mice induced by Abeta 42 fibrils. Science. 2001 Aug 24;293(5534):1491-5. PubMed.

    View all comments by Samuel Gandy
  2. The authors bring up some interesting points and I concur that sex steroid hormones probably play a role, whether directly or indirectly, in the pathogenesis of AD. However, the authors' conclusions fail to consider at least two confounding factors. One might suspect that there is a gender difference in the expression of sex steroid hormone receptors, yet the experiment was only performed on female rats. It would be interesting to see what would occur if gonadectomized male rats were administered estrogen. It might well be that one would see the same results of administering testosterone to gonadectomized female rats. In addition, the effect of alterations in gonadotropin secretion was not considered. Gonadotropins have been shown to upregulate CDK 5 in reproductive tissues (Musa 2000). Therefore, in vivo, any effects of the sex steroids might be partially mediated by alterations in gondadotropin secretion.

    One other issue that may be of importance is that the experiment was performed during the peri-pubertal period. Future experiments should probably be delayed until the rats have completed puberty. This is because sex steroid receptor expression might be developmentally regulated.


    . Effects of luteinizing hormone, follicle-stimulating hormone, and epidermal growth factor on expression and kinase activity of cyclin-dependent kinase 5 in Leydig TM3 and Sertoli TM4 cell lines. J Androl. 2000 May-Jun;21(3):392-402. PubMed.

    View all comments by Richard Bowen

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  1. Testosterone and Alzheimer's—a Possible Tau Connection