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. Author manuscript; available in PMC: 2019 Apr 29.
Published in final edited form as: Neuropharmacology. 2018 Jun 7;138:160–169. doi: 10.1016/j.neuropharm.2018.06.009

Table 1.

Experimental design and animal numbers used per group. None of sham operated animals died in this study. Average mortality was 8.8% in the experimental animals. No significant difference between treated and untreated subgroups was observed in the mortality. BWC, brain water content; IHC, immunohistochemistry; MPO, myeloperoxidase; ICH + HG, hyperglycemic intracerebral hemorrhage; Vehicle, 0.9% sterile NaCl; siRNA, small interfering ribonucleic acid; Coumermycin A1, an agonist of JAK2.

Groups Neuro test BWC
Western blot IHC MPO Mortality
Sum
24 h 72 h 24 h 72 h
Time course study (n = 6; 9 per group): Sham 6 3 9
ICH + HG (6, 12, 24, 48, 72 h) 30 (5) 3 5 (13%) 38
Outcome and Mechanism study:
Sham 6 6 12 (6 + 6)
ICH + HG + Vehicle 6 (1) 6 (2) 6 (1) 3 2 (12%) 2 (25%) 25 (17 + 8)
ICH + HG + rOPN 18 (1) 6 (1) 6 3 1 (4%) 1 (14%) 35 (28 + 7)
ICH + HG + Scramble siRNA 6 3 9
ICH + HG + Integrin-β1 siRNA 6 3 9
ICH + HG + rOPN + Coumermycin A1 6 (1) 3 (1) 2 (18%) 11
Total 30 18 66 21 13 (8.8%) 148