Why the study?
Does the selective M2 antagonist AF-DX116 improve orthostatic hypotension in a SART-stressed rat model of autonomic imbalance?
Does the selective M2 antagonist AF-DX116 improve orthostatic hypotension in a SART-stressed rat model of autonomic imbalance?
In a rat model of autonomic imbalance, the selective M2 muscarinic receptor antagonist AF-DX116 significantly improved orthostatic hypotension, suggesting a primary role for M2 receptors in this condition.
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Supports M2 antagonism in autonomic imbalance models; hypothesis-generating and requires human trials before clinical consideration.
SART (specific alternation of rhythm in temperature)-stressed rats are an animal model of autonomic imbalance created by exposing animals to repeated cold stress. The SART-stressed rats have been shown to easily develop orthostatic hypotension (OH). In this study, effects of AF-DX116, a selective M(2) antagonist, and other muscarinic receptor antagonists on OH were investigated in SART-stressed and unstressed rats. Each anesthetized rat was canulated into the left common carotid artery, and blood pressure (BP) and heart rate were measured. Stimulation for postural change was initiated by head-up tilting. As the indices of OH, the maximum fall of BP, % reflex (recovery from maximum fall), and the area enclosed between the baseline and the recovery curve for BP (AUC) were used. Large AUC and small % reflex in SART-stressed rats were changed, becoming similar to those of the unstressed rats by AF-DX116 and methoctoramine. Atropine and methylatropine had similar effects to AF-DX116. However, the effects of methoctoramine, atropine, and methylatropine were less than that of AF-DX116. Pirenzepine was not effective. In conclusion, it was suggested in SART-stressed rats that OH was related to hyperactivity in the parasympathetic nerve and the M(2) receptor played the major role in OH.
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Hata et al. (2005) studied this question.
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