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Morphine microinjected into the periaqueductal gray has differential effects on 3 classes of medullary neurons
Abstract:
The effects of microinjection of 5-10 micrograms of morphine into the midbrain periaqueductal gray (PAG) on the activity of neurons in the rostral ventral medulla (RVM) were studied in lightly anesthetized rats. Based on the relationship between changes in neuronal activity and the occurrence of the tail-flick reflex (TF), RVM neurons were divided into 3 groups: off-cells, on-cells and neutral cells. The off-cells exhibited an abrupt pause and the on-cells an acceleration beginning just prior to the occurrence of the TF. Neutral cell firing did not change at the time of the TF. Microinjections of morphine into the PAG which inhibited the TF had differential effects on the spontaneous activity of the 3 groups of neurons in RVM. Off-cells showed an increase and on-cells a decrease in spontaneous activity which preceded the inhibition of the TF. These microinjections also reduced the TF-related responses of off- and on-cells. The effects on cell activity were reversed by systemically administered naloxone and were not seen following microinjections which failed to block the TF. Neutral cell activity was unchanged following microinjection of morphine into the PAG. These results support the hypothesis that off- and on-cells in the RVM mediate the effects of microinjection of morphine into the PAG on spinal nociceptive reflexes.
Insights
Morphine microinjections into the periaqueductal gray (PAG) alter rostral ventral medulla (RVM) neuron activity, affecting pain reflexes. Off-cells and on-cells in the RVM mediate these morphine-induced changes in spinal nociceptive reflexes.
Area of Science:
- Neuroscience
- Pharmacology
- Pain Research
Background:
- The periaqueductal gray (PAG) plays a crucial role in pain modulation.
- Neurons in the rostral ventral medulla (RVM) are involved in processing nociceptive information.
Purpose of the Study:
- To investigate the effects of morphine microinjections into the PAG on RVM neuronal activity.
- To determine the role of RVM neurons in mediating morphine's analgesic effects.
Main Methods:
- Microinjection of morphine into the PAG of anesthetized rats.
- Recording neuronal activity in the RVM.
- Correlation of neuronal activity with the tail-flick reflex (TF).
- Administration of naloxone to assess opioid receptor involvement.
Main Results:
- Morphine in the PAG inhibited the tail-flick reflex.
- Spontaneous activity of RVM off-cells increased, while on-cells decreased, preceding TF inhibition.
- Morphine reduced TF-related responses of off- and on-cells.
- Naloxone reversed these effects, and non-inhibitory microinjections had no effect.
Conclusions:
- RVM off- and on-cells are critical mediators of morphine's effects on spinal nociceptive reflexes.
- These findings support a model where PAG-mediated analgesia involves modulation of RVM neuronal activity.
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