Microinjection of angiotensin II in the caudal ventrolateral medulla induces hyperalgesia |
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Authors: | J Marques-Lopes M Pinto D Pinho M Morato D Patinha A Albino-Teixeira I Tavares |
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Institution: | 1. Institute of Pharmacology and Therapeutics, Faculty of Medicine of Porto, and Institute for Molecular and Cell Biology, University of Porto, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal;2. Pharmacology Department, Faculty of Pharmacy of Porto, University of Porto, Rua Aníbal Cunha 164, 4099-030 Porto, Portugal;3. Institute of Histology and Embryology, Faculty of Medicine of Porto and Institute for Molecular and Cell Biology, University of Porto, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal |
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Abstract: | Nociceptive transmission from the spinal cord is controlled by supraspinal pain modulating systems that include the caudal ventrolateral medulla (CVLM). The neuropeptide angiotensin II (Ang II) has multiple effects in the CNS and at the medulla oblongata. Here we evaluated the expression of angiotensin type 1 (AT1) receptors in spinally-projecting CVLM neurons, and tested the effect of direct application of exogenous Ang II in the CVLM on nociceptive behaviors. Although AT1-immunoreactive neurons occurred in the CVLM, only 3% of AT1-positive neurons were found to project to the dorsal horn, using double-immunodetection of the retrograde tracer cholera toxin subunit B. In behavioral studies, administration of Ang II (100 pmol) in the CVLM gave rise to hyperalgesia in both the tail-flick and formalin tests. This hyperalgesia was significantly attenuated by local administration of the AT1 antagonist losartan. The present study demonstrates that Ang II can act on AT1 receptors in the CVLM to modulate nociception. The effect on spinal nociceptive processing is likely indirect, since few AT1-expressing CVLM neurons were found to project to the spinal cord. The renin-angiotensin system may also play a role in other supraspinal areas implicated in pain modulation. |
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Keywords: | pain control system renin-angiotensin AT1 receptors angiotensin receptor antagonists descending pain modulation rat |
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