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. Author manuscript; available in PMC: 2021 Feb 1.
Published in final edited form as: Neurocrit Care. 2020 Feb;32(1):238–251. doi: 10.1007/s12028-018-0650-5

Table 6.

Cohorts in which scattered cell death was detected after experimental SAH

Species SAH method Time of assessment (days) Histological method to show cell death Region Refs.

Mouse PCI 2 FJ, TUNEL, caspase 3 C [43]
Mouse PCI 2 FJ C, H [41]
Mouse PCI 2 TUNEL C, SC, H [40]
Mouse PCI 2 TUNEL C, SC, H [39]
Mouse CMI 7 NeuN C [37]
Mouse CMI 7 Nissl C, H [38]
Mouse EVP 1, 14 FJ (day 1), NeuN (day 14) C, H [17]
Rat PCI 1, 3 Caspase 3 & TUNEL (day 1), Nissl (day 3) C [70]
Rat CMI 3, 5 H&E C, H [16]
Rat EVP 7 Cresyl violet H [80]
Rat EVP 2–7 Cresyl violet, FJ, TUNEL H [77]
Rat EVP 5 Cresyl violet H [72]
Rat EVP 1 FJ, TUNEL C [83]
Rabbit CMI 1 TUNEL and Nissl C [70]
Primate PVC 7 Cresyl violet C [143]

Studies are sorted by species and SAH method

C cortex, CMI cisterna magna blood injection ×1–3, EVP endovascular perforation of internal carotid artery terminus, FJ fluoro-Jade staining, H hippocampus, H&E hematoxylin–eosin staining, PCI prechiasmatic blood injection, PVC perivascular clot placement, SAH subarachnoid hemorrhage, SC subcortex, TUNEL terminal deoxynucleotidyl transferase dUTP nick end labeling