<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-19T01:08:42Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/13589" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/13589</identifier><datestamp>2026-10-18T20:41:19Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Brachial Artery Vasospasm Caused by Cervical Dorsal Root Ganglion Degeneration After Subarachnoid Hemorrhage: An Experimental Study</dc:title><dc:creator>Kayacı, Selim</dc:creator><dc:creator>Çakir, Tayfun</dc:creator><dc:creator>Aydın, Mehmet Dumlu</dc:creator><dc:creator>Kanat, Ayhan</dc:creator><dc:creator>Omeroglu, Muhammed</dc:creator><dc:creator>Levent, Akin</dc:creator><dc:creator>Kantarci, A. Mecit</dc:creator><dc:creator>Diyarbakırlı, Semih</dc:creator><dc:creator>Demirci, Elif</dc:creator><dc:subject>Brachial artery</dc:subject><dc:subject>Dorsal root ganglion</dc:subject><dc:subject>Hypertension</dc:subject><dc:subject>Subarachnoid hemorrhage</dc:subject><dc:subject>Vasospasm</dc:subject><dc:subject>Animals</dc:subject><dc:subject>Disease Models, Animal</dc:subject><dc:subject>Ganglia, Spinal</dc:subject><dc:subject>Male</dc:subject><dc:subject>Nerve Degeneration</dc:subject><dc:subject>Rabbits</dc:subject><dc:subject>Vasospasm, Intracranial</dc:subject><dc:subject>acepromazine</dc:subject><dc:subject>iohexol</dc:subject><dc:subject>ketamine</dc:subject><dc:subject>lidocaine</dc:subject><dc:subject>animal experiment</dc:subject><dc:subject>animal model</dc:subject><dc:subject>animal tissue</dc:subject><dc:subject>apoptosis</dc:subject><dc:subject>arterial oxygen saturation</dc:subject><dc:subject>Article</dc:subject><dc:subject>brachial artery vasospasm</dc:subject><dc:subject>bradypnea</dc:subject><dc:subject>brain perfusion</dc:subject><dc:subject>breathing rate</dc:subject><dc:subject>computed tomographic angiography</dc:subject><dc:subject>computer assisted tomography</dc:subject><dc:subject>controlled study</dc:subject><dc:subject>electrocardiography</dc:subject><dc:description>Purpose: Subarachnoid hemorrhage (SAH) may lead to vasospasm in various vessels. The cervical nerves have a vasodilatory effect on the upper extremity arteries. The aim of this study was to investigate if there is a relationship between C6 dorsal root ganglion (DRG) degeneration and brachial artery (BA) vasospasm after spinal SAH. Methods: This experimental study was conducted on 23 rabbits. The animals were divided into 3 groups: control (n = 5), SHAM (n = 5), and study group (n = 13). One cubic centimeter (cc) of serum saline was injected into the cisterna magna of animals of the SHAM group; the same procedure was performed by 1 cc of homologous blood in the study group. Degenerated neuron densities (DNDs) of DRGs (n/mm3) at C6 levels and BA vasospasm indexes (VSI; wall surface/lumen surface) of all animals were determined and results were analyzed statistically. Results: Mean VSI values of BAs and DNDs of C6DRGs of the control, SHAM, and study groups were estimated as 10 ± 3/1.12 ± 0.11 n/mm3, 34 ± 9/1.27 ± 0.24 n/mm3, and 1031 ± 145/2.93 ± 0.78 n/mm3, respectively. Mean DNDs and VSI values were statistically significantly different between the control and study groups (P &lt; 0.0001). Conclusions: C6DRG degeneration may be considered as an important factor in the etiopathogenesis of severe BA vasospasm after SAH. © 2019 Elsevier Inc.</dc:description><dc:publisher>Elsevier Inc.</dc:publisher><dc:date>2019</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/13589</dc:identifier><dc:identifier>https://doi.org/10.1016/j.wneu.2019.03.007</dc:identifier><dc:identifier>1878-8750</dc:identifier><dc:language>en</dc:language><dc:relation>World Neurosurgery</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/13589</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>