Single units activities in ventral posterior and posterior group thalamic nuclei during nociceptive and non nociceptive stimulations in the cat.

G. Guilbaud, D. Caille, J. M. Besson, G. Benelli

PubMed · 1977 · 70 citations · 0 references

Concepts

TL;DR

The study aimed to determine how posterior thalamic nuclei contribute to pain processing in hyperventilated, unanesthetized cats. Researchers recorded activity from 135 single units in posterior and ventro‑posterior nuclei while delivering non‑noxious touch and noxious pinches or bradykinin injections, comparing responses between the two nuclei. Noxious stimuli selectively activated units in posterior group nuclei (POm, POl, suprageniculate, Mgmc, lateral posterior ventral part), with two subpopulations—noxious‑only and dual‑modality—whereas ventro‑posterior units remained unresponsive, underscoring the posterior nuclei’s role in pain.

Abstract

The purpose of this study was to define, in hyperventilated and unanesthetized cats, the role of the posterior thalamic nuclei in pain mechanisms. Unit activities of these structures were compared to those of the ventro-posterior nucleus during non-noxious (touch, brushing) and noxious stimulations (pinches and intra-arterial injections of bradykinin into the limbs). 135 cells with somatic inputs and clear peripheral excitatory receptive field were studied. The cells driven by noxious stimulations were located in the posterior group nuclei as anatomically defined by Rinvik. These units, preferentially excited from contralateral receptive fields, were localized in POm, POl, suprageniculate nuclei, the magnocellular division of the medial geniculate body (Mgmc) and the ventral part of the lateral posterior nucleus. At this level two groups of units were found: those driven only by noxious stimulations and those driven by both noxious and non-noxious stimulations. On contrast, cells recorded at the levels of the VPm and VPl were not activated by noxious stimuli. These results emphasize the role of the posterior thalamic nuclei in pain processing.