AI Article Synopsis

  • The study investigates the impact of arginine-vasopressin (AVP) on long-term potentiation (LTP) in the dentate gyrus of anesthetized rats.
  • Administering AVP before tetanization significantly enhanced evoked potentials, with increases observed just one minute after tetanization, peaking at 100% above baseline over two hours.
  • Results contrast with previous in vitro findings, highlighting differences in how hormone interactions influence physiological responses in living organisms versus controlled laboratory settings.

Article Abstract

We studied the effects of the neuropeptide arginine-vasopressin (AVP) on the long-term potentiation (LTP) paradigm in the dentate gyrus (DG) of urethane intact anesthetized rats. Intracerebroventricular injection of 1 microg of the hormone in 1 microl of physiological solution 3 min before tetanization, produced a significant increase in both components of the perforant path-evoked potentials (EP) in the DG. The effects were already evident 1 min after tetanization. Amplitude of the EPs increased continuously for the 2h of recording time, reaching values 100% above baseline, reference levels. In contrast, in previous in vitro studies, enhancement of LTP with AVP appeared only after 15 min of exposure of the hippocampal slice to the hormone, increased EPSPs were no higher than 50% from baseline, reached a plateau at 40 min decreasing slowly thereafter. Not only quantitative but also qualitative differences can be observed between in vitro and in vivo intact preparations in response to identical hormones. This study emphasizes the importance of hormone neurotransmitter interactions in determining electrophysiological characteristics of response to AVP.

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http://dx.doi.org/10.1016/s0361-9230(02)00961-9DOI Listing

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