4.4 Article

Ventrolateral periaqueductal gray matter integrative system of defense and antinociception

Journal

PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
Volume 474, Issue 4, Pages 469-480

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00424-022-02672-0

Keywords

Defensive immobility; Antinociception; Respiratory function; Ventrolateral column of periaqueductal gray matter

Categories

Funding

  1. National Council of Scientific and Technological Development (CNPq) [483763/2010-1, 474853/2013-6]
  2. Sao Paulo Research Foundation (FAPESP) [2009/54014-7, 2016/18218-0, 2016/17681-9]
  3. Pro-Rectory of the University of Sao Paulo (USP) Research Grant (NAP-USPNuPNE) [IaPq2012-156-USP-12.1.25440.01.6]
  4. CNPq [134564/0, 301905/2010-0, 301341/2015-0, 150806/2021-3, 501858/2005-9, 500896/2008-9, 505461/2010-2]
  5. FAPESP [2014/10742-7, 785219, 881603, 2015/10313-1, 2017/13560-5, 02/01497-1]
  6. The Academy of Sciences for the Developing World (TWAS)-CNPq [190316/2010-1]
  7. Neurologia-PNPDCAPES [001]
  8. CAPES [001, CAPES/PROEX 33002029012P3]

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Defensive immobility is an adaptive response in rodents during unavoidable threats, regulated by the ventrolateral periaqueductal gray matter (vlPAG) and associated with changes in pain perception and breathing. Chemical stimulation of vlPAG induces defensive immobility and alters respiratory responses.
Defensive responses are neurophysiological processes crucial for survival during threatening situations. Defensive immobility is a common adaptive response, in rodents, elaborated by ventrolateral periaqueductal gray matter (vlPAG) when threat is unavoidable. It is associated with somatosensory and autonomic reactions such as alteration in the sensation of pain and rate of respiration. In this study, defensive immobility was assessed by chemical stimulation of vlPAG with different doses of NMDA (0.1, 0.3, and 0.6 nmol). After elicitation of defensive immobility, antinociceptive and respiratory response tests were also performed. Results revealed that defensive immobility was followed by a decrease in the nociceptive perception. Furthermore, the lowest dose of NMDA induced antinociceptive response without eliciting defensive immobility. During defensive immobility, respiratory responses were also disturbed. Interestingly, respiratory rate was increased and interspersed with prolonged expiratory phase of breathing. These findings suggest that vlPAG integrates three different defensive behavioral responses, contributing to the most effective defensive strategies during threatening situations.

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