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Am J Physiol Regul Integr Comp Physiol (August 29, 2002). doi:10.1152/ajpregu.00191.2002
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Articles in PresS, published online ahead of print August 29, 2002
Am J Physiol Regu Physiol, 10.1152/ajpregu.00191.2002
Submitted on March 29, 2002
Accepted on August 22, 2002

Adrenomedullin influences magnocellular and parvocellular neurons of the paraventricular nucleus through separate mechanisms

Matthew J Follwell1 and Alastair V Ferguson1*

1 Department of Physiology, Queen's University, Kingston, Ont., Canada

* To whom correspondence should be addressed. E-mail: fergusna{at}post.queensu.ca.

We have previously reported that adrenomedullin (AM) decreases blood pressure following microinjection into the paraventricular nucleus of the hypothalamus (PVN) of the rat. Using whole-cell recordings in rat hypothalamic slice preparations, we have characterized the effects of AM on electrophysiologically identified PVN neurons, and described the membrane events underlying such actions. AM hyperpolarized magnocellular (Type I) neurons in a dose dependent manner, a response associated with an increase in the frequency and amplitude of inhibitory post-synaptic potentials (IPSPs). Blockade of action potentials with tetrodotoxin (TTX) abolished AM effects on membrane potential and synaptic activity in magnocellular neurons, suggesting direct actions on inhibitory interneurons. Furthermore, blockade of inhibitory synaptic transmission with the GABAA receptor antagonist bicuculline methiodide (BMI) also abolished AM effects on membrane potential in magnocellular neurons. In contrast parvocellular (Type II) neurons depolarized following AM-receptor activation. AM effects on parvocellular neurons were dose dependent and were maintained in the presence of TTX indicating direct effects on this population of neurons. Voltage clamp recordings from parvocellular neurons showed AM enhance a non-selective cationic conductance suggesting a potential mechanism through which AM influences membrane potential. These observations show clear population specific actions of AM on separate identified groups of PVN neurons. Such effects on magnocellular neurons likely contribute to the hypotensive actions of this peptide in PVN. While the effects on parvocellular neurons may also contribute to such cardiovascular effects of AM, it is more likely that actions on this population of PVN neurons underlie the previously demonstrated activational effects of AM on the HPA axis.




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