Estrogen administration modulates Parvalbumin expression in the hippocampus of trimethyltin-treated rats

Trimethyltin (TMT)-induced hippocampal injury represents a suitable instrument not only to study neuronal and glial responses during neurogeneration and intracellular signaling pathways associated with neuronal damage, but also to validate new strategies to clarify brain repair mechanisms [1-3]. Rats exposed to TMT show severe loss of pyramidal neurons in the CA1 and CA3 hippocampal subfields, showing a subacute pattern developing over three weeks, associated with astroglial and microglial activation, enhanced neurogenesis, seizures and cognitive impairment [1-3]. Since it is known that 17 beta-estradiol (E2) plays a role in neuroprotection and influences GABAergic transmission, also by modulating parvalbumin (PV) expression [4, 5], in the present study we explored, in the hippocampus of TMT-treated ovariectomised rats, the effects of E2 administration. After TMT or saline treatment, animals (n=6/group) received two i.p. E2 doses (100microg/rat) or vehicle, and were sacrificed on post-treatment day 7. Unbiased stereological analysis of Fluoro Jade-, GAD67- and PV-stained hippocampal sections evidenced that, while E2 administration does not significantly influence the extent of neuronal death, as well as the increase in the number of GAD67 expressing interneurons caused by the toxicant, it induces a significant increase in the number of PV positive hippocampal neurons (p
Italian Journal of Anatomy and Embryology, Vol 119, No 1 (Supplement) 2014