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Rather, it suggests the pain process may be initiated in ways scientists still don't understand, by things less palpable than losing a filling or stubbing a toe.
AVP is the most important bioactive substance in PVN regulating pain process.
The data suggested that OXT in the CdN was involved in this pain process via OXT receptors.
The communication was designed to investigate the interaction between AVP and Ach in the rat CdN during the pain process.
The communication was designed to investigate the interaction between AVP and NA in the rat PVN during the pain process.
The communication was designed to investigate the source of OXT in the rat CdN during pain process using the methods of push pull perfusion and radioimmunoassay.
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We are studying an endogenous, oxytocinergic analgesia system to obtain more information about normal and pathological pain processes.
Noxious peripheral inputs and central descending modulation are integrated within trigeminocervical (TCC) neurons, the net result of which is head pain, processed within the thalamocortical neurons.
The nociceptin system seems to be involved in modulation of acute nociceptive stimulation and in chronic pain processes, e.g. inflammation and neuropathy.
This could potentially help to identify individuals at risk and, if coupled to a greater mechanistic understanding of the underlying pain processes, may direct preemptive pharmacological treatment.
Importantly, the alteration of pain processes is strongly related to IBS symptoms, suggesting that altered pain processes may contribute to the pathophysiology of IBS [ 16].
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