Journal
JOURNAL OF PHYSIOLOGY-LONDON
Volume 531, Issue 2, Pages 515-526Publisher
WILEY
DOI: 10.1111/j.1469-7793.2001.0515i.x
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1. It has been previously shown that spreading neuronal activation can generate a cortical spreading ischaemia (CSI) in rats. The purpose of the present study was to investigate whether vasodilators cause CSI to revert to a normal cortical spreading depression (CSD). 2. A KCl-induced CSD travelled from an open cranial window to a closed window where the cortex was superfused with physiological artificial cerebrospinal fluid (ACSF). Bt the closed window, recordings revealed a short-lasting negative slow potential shift accompanied by a variable, small and short initial hypoperfusion followed by hyperaemia and then oligaemia. 3. In contrast, spreading neuronal activation locally induced CSI at the closed window when ACSF contained a NO synthase (NOS) inhibitor, N-G-nitro-L-arginine, and an increased K+ concentration ([K+](ACSF)). CSI was characterised by a sharp and prolonged initial cerebral blood flow decrease to 29 +/- 11 % of the baseline and a prolonged negative potential shift. 4. Go-application of a NO donor, S-nitroso-N-acetylpenicillamine, and NOS inhibitor with high [K+](ACSF) re-established a short-lasting negative potential shift and spreading hyperaemia typical of CSD. Similarly, the NO-independent vasodilator papaverine caused CSI to revert to a pattern characteristic of CSD. 5. In acute rat brain slices, NOS inhibition and high [K+](ACSF) did not prolong the negative slow potential shift compared to that induced by high [K+](ACSF) alone. 6. The data indicate that the delayed recovery of the slow potential was caused by vasoconstriction during application of high [K+](ACSF) and a NOS inhibitor in vivo. This supports the possibility of a vicious circle: spreading neuronal activation induces vasoconstriction, and vasoconstriction prevents repolarisation during CSI. Speculatively, this pathogenetic process could be involved in migraine-induced stroke.
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