Key result
Intrathecal administration of neurotensin (3000 µM) in rats caused dose-related hypotension (-25 mmHg), bradycardia (-26 beats/min), and sympathoinhibition (-26% sSNA).
Intrathecal neurotensin plays a role in regulating spinal cardiovascular function by inducing hypotension, sympathoinhibition, and bradycardia in a rat model.
Reveals spinal neurotensin involvement in autonomic cardiovascular control in rats; leaves open translation to clinical settings.
BACKGROUND AND PURPOSE: The neuromodulatory effects of the gut-neuropeptide neurotensin on sympathetic vasomotor tone, central respiratory drive and adaptive reflexes in the spinal cord, are not known. EXPERIMENTAL APPROACH: Neurotensin (0.5 µM-3 mM) was administered into the intrathecal (i.t.) space at the sixth thoracic spinal cord segment in urethane-anaesthetized, paralysed, vagotomized male Sprague-Dawley rats. Pulsatile arterial pressure, splanchnic sympathetic nerve activity (sSNA), phrenic nerve activity, ECG and end-tidal CO(2) were recorded. KEY RESULTS: Neurotensin caused a dose-related hypotension, sympathoinhibition and bradycardia. The maximum effects were observed at 3000 µM, where the decreases in mean arterial pressure (MAP), heart rate (HR) and sSNA reached -25 mmHg, -26 beats min(-1) and -26% from baseline, respectively. The sympathetic baroreflex was enhanced. Changes in central respiratory drive were characterized by a fall in the amplitude of the phrenic nerve activity. Finally, administration of SR 142948A (5 mM), a potent, selective antagonist at neurotensin receptors, caused a potent hypotension (-35 mmHg), bradycardia (-54 beats min(-1) ) and sympathoinhibition (-44%). A reduction in the amplitude and frequency of the phrenic nerve activity was also observed. CONCLUSIONS AND IMPLICATIONS: The data demonstrate that neurotensin plays an important role in the regulation of spinal cardiovascular function, affecting both tone and adaptive reflexes.
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Zogovic et al. (2011) studied this question. Intrathecal neurotensin vs. Baseline was evaluated on Mean arterial pressure, heart rate, and splanchnic sympathetic nerve activity. Intrathecal administration of neurotensin (3000 µM) in rats caused dose-related hypotension (-25 mmHg), bradycardia (-26 beats/min), and sympathoinhibition (-26% sSNA).
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