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Furthermore, a change in conductance best reflects a change Dolutegravir in vitro in vascular tone rather than changes in resistance (Lautt, 1989). Subject comparisons were made across three exercise WLs (rest, Ex90 and Ex130) and across two conditions (control and prazosin). Two (3 �� 2) factor ANOVA with repeated measures across each factor was used to assess the differences in haemodynamic variables, transfer function phase, gain and coherence in each frequency (SigmaStat; Jandel Scientific Software, SPSS, Chicago, IL, USA). Significant main effects were analysed using a Student�CNewman�CKeuls post hoc test. There were no significant interactions. Statistical significance was set at P �� SEM. A bolus dose of PE produced an average increase in MAP of 12 �� 1 mmHg; however, following prazosin, the same bolus dose of PE resulted in an increase in MAP of only 3.2 �� 1 mmHg, indicating a 74 �� 2% blockade of the pressor response mediated by ��1-adrenergic receptor blockade. At the end of the experimental protocol, there was a 71 �� 4% blockade of the blood pressure response, confirming that the prazosin blockade of the ��1-adrenergic receptor-mediated blood pressure increase was maintained throughout the protocol. The mean values for the cardiovascular and haemodynamic variables obtained at rest and for the two exercise WLs during control conditions and with prazosin are presented in Table 1. An increase in MAP at Ex130 was observed compared with Ex90 (P= 0.040) and rest (P CDK9 in the control conditions. The Ex90 workload also Obeticholic Acid nmr resulted in an increase in MAP from rest (P= 0.044) in the control conditions. Following prazosin, however, an overall decrease in MAP from the control conditions was observed at rest and during both the exercise WLs (P