{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,30]],"date-time":"2025-10-30T11:30:44Z","timestamp":1761823844040,"version":"3.40.3"},"reference-count":24,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:sec><jats:title>OBJECTIVE<\/jats:title><jats:p>Although cortical spreading depolarization (CSD) has been observed during the early phase of subarachnoid hemorrhage (SAH) in clinical settings, the pathogenicity of CSD is unclear. The aim of this study is to elucidate the effects of loss of membrane potential on neuronal damage during the acute phase of SAH.<\/jats:p><\/jats:sec><jats:sec><jats:title>METHODS<\/jats:title><jats:p>Twenty-four rats were subjected to SAH by the perforation method. The propagation of depolarization in the brain cortex was examined by using electrodes to monitor 2 direct-current (DC) potentials and obtaining NADH (reduced nicotinamide adenine dinucleotide) fluorescence images while exposing the parietal-temporal cortex to ultraviolet light. Cerebral blood flow (CBF) was monitored in the vicinity of the lateral electrode. Twenty-four hours after onset of SAH, histological damage was evaluated at the DC potential recording sites.<\/jats:p><\/jats:sec><jats:sec><jats:title>RESULTS<\/jats:title><jats:p>Changes in DC potentials (n = 48 in total) were sorted into 3 types according to the appearance of ischemic depolarization in the entire hemisphere following induction of SAH. In Type 1 changes (n = 21), ischemic depolarization was not observed during a 1-hour observation period. In Type 2 changes (n = 13), the DC potential demonstrated ischemic depolarization on initiation of SAH and recovered 80% from the maximal DC deflection during a 1-hour observation period (33.3 \u00b1 15.8 minutes). In Type 3 changes (n = 14), the DC potential displayed ischemic depolarization and did not recover during a 1-hour observation period. Histological evaluations at DC potential recording sites showed intact tissue at all sites in the Type 1 group, whereas in the Type 2 and Type 3 groups neuronal damage of varying severity was observed depending on the duration of ischemic depolarization. The duration of depolarization that causes injury to 50% of neurons (P<jats:sub>50<\/jats:sub>) was estimated to be 22.4 minutes (95% confidence intervals 17.0\u201330.3 minutes). CSD was observed in 3 rats at 6 sites in the Type 1 group 5.1 \u00b1 2.2 minutes after initiation of SAH. On NADH fluorescence images CSD was initially observed in the anterior cortex; it propagated through the entire hemisphere in the direction of the occipital cortex at a rate of 3 mm\/minute, with repolarization in 2.3 \u00b1 1.2 minutes. DC potential recording sites that had undergone CSD were found to have intact tissue 24 hours later. Compared with depolarization that caused 50% neuronal damage, the duration of CSD was too short to cause histological damage.<\/jats:p><\/jats:sec><jats:sec><jats:title>CONCLUSIONS<\/jats:title><jats:p>CSD was successfully visualized using NADH fluorescence. It propagated from the anterior to the posterior cortex along with an increase in CBF. The duration of depolarization in CSD (2.3 \u00b1 1.2 minutes) was far shorter than that causing 50% neuronal damage (22.4 minutes) and was not associated with histological damage in the current experimental setting.<\/jats:p><\/jats:sec>","DOI":"10.3171\/2016.9.jns161385","type":"journal-article","created":{"date-parts":[[2017,1,27]],"date-time":"2017-01-27T14:59:34Z","timestamp":1485529174000},"page":"137-143","source":"Crossref","is-referenced-by-count":9,"title":["NADH fluorescence imaging and the histological impact of cortical spreading depolarization during the acute phase of subarachnoid hemorrhage in rats"],"prefix":"10.3171","volume":"128","author":[{"given":"Tomohisa","family":"Shimizu","sequence":"first","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tomohito","family":"Hishikawa","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shingo","family":"Nishihiro","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yukei","family":"Shinji","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuji","family":"Takasugi","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jun","family":"Haruma","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masafumi","family":"Hiramatsu","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hirokazu","family":"Kawase","sequence":"additional","affiliation":[{"name":"Department of Anesthesiology and Resuscitology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sachiko","family":"Sato","sequence":"additional","affiliation":[{"name":"Department of Anesthesiology and Resuscitology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ryoichi","family":"Mizoue","sequence":"additional","affiliation":[{"name":"Department of Anesthesiology and Resuscitology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoshimasa","family":"Takeda","sequence":"additional","affiliation":[{"name":"Department of Anesthesiology and Resuscitology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenji","family":"Sugiu","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroshi","family":"Morimatsu","sequence":"additional","affiliation":[{"name":"Department of Anesthesiology and Resuscitology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Isao","family":"Date","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1754","reference":[{"key":"b1-jns161385","series-title":"Magn Reson Med","first-page":"110","article-title":"Spreading waves of transient and prolonged decreases in water diffusion after subarachnoid hemorrhage in rats","volume":"44","author":"Beaulieu C,","year":"2000","unstructured":"Beaulieu C, Busch E, de Crespigny A, Moseley ME: Spreading waves of transient and prolonged decreases in water diffusion after subarachnoid hemorrhage in rats. 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