Rapid adenosine release in the nucleus tractus solitarii during defence response in rats: real-time measurement in vivo
We have measured the release of adenosine and inosine from the dorsal surface of the brainstem and from within the nucleus tractus solitarii (NTS) during the defence response evoked by hypothalamic stimulation in the anaesthetised rat. At the surface of the brainstem, only release of inosine was det...
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Veröffentlicht in: | The Journal of physiology 2002-10, Vol.544 (1), p.149-160 |
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Zusammenfassung: | We have measured the release of adenosine and inosine from the dorsal surface of the brainstem and from within the nucleus
tractus solitarii (NTS) during the defence response evoked by hypothalamic stimulation in the anaesthetised rat. At the surface
of the brainstem, only release of inosine was detected on hypothalamic defence area stimulation. This inosine signal was greatly
reduced by addition of the ecto-5â²-nucleotidase inhibitor α,β-methylene ADP (200 μM), suggesting that the inosine arose from
adenosine that was produced in the extracellular space by the prior release of ATP. By placing a microelectrode biosensor
into the NTS under stereotaxic control we have recorded release of adenosine within this nucleus. By contrast to the brainstem
surface, a fast increase in adenosine, accompanied only by a much smaller change in inosine levels, was seen following stimulation
of the hypothalamic defence area. The release of adenosine following hypothalamic stimulation was mainly confined to a narrow
region of the NTS some 500 μm in length around the level of the obex. Interestingly the release of adenosine was depletable:
when the defence reaction was evoked at short time intervals, much less adenosine was released on the second stimulus. Our
novel techniques have given unprecedented real-time measurement and localisation of adenosine release in vivo and demonstrate that adenosine is released at the right time and in sufficient quantities to contribute to the cardiovascular
components of the defence reaction. |
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ISSN: | 0022-3751 1469-7793 |
DOI: | 10.1113/jphysiol.2002.024158 |