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. 2014 Sep 5;171(22):5076–5092. doi: 10.1111/bph.12824

Table 1.

Study overview study 1 and study 2

Study 1
Study Measures Study designs Compound Dose (mg kg−1) Strain Number of rats
1 Single administrations of different doses on separate days MAP, HR and SV (CO and TPR) Day 1: vehicle Following days: a different dose each day Amiloride 10 SHR 3
Amlodipinec 0.3, 1, 3, 10 SHR 2
WKY 2
Enalapril 3, 10, 30 SHR 4d
Fasudil 3, 10, 30 SHR 4
HCTZa,c 0.1, 0.3, 1, 3 SHR 2
WKY 2
HCTZb 10, 30 SHR 4
Prazosinc 0.04, 0.2, 1, 5 SHR 2
WKY 1
Study 2
Study Measures Study designs Number of rats (SHR)
2 Single, sequential or combined administration of atropine (10 mg kg−1) and/or propranolol (30 mg kg−1) MAP, HR and SV (CO and TPR) Vehicle followed by vehicle 3 h later 2
Atropine followed by propranolol 3 h later 3d
Propranolol followed by atropine 3 h later 3
Combination of atropine and propranolol 1
Atropine followed by no dosing 3d
Propranolol followed by no dosing 3
1

First occasion.

2

Second occasion.

3

Data from SHR were previously used for the characterization of the CVS model (Snelder et al., 2013a).

4

Data from one rat were excluded for model development as this rat learned how to disconnect its flow cable and responded more strongly than all other rats resulting in a low MAP.