Neuromodulation using ultra low frequency current waveform reversibly blocks axonal conduction and chronic pain

2021 ◽  
Vol 13 (608) ◽  
Author(s):  
Martyn G. Jones ◽  
Evan R. Rogers ◽  
James P. Harris ◽  
Andrew Sullivan ◽  
D. Michael Ackermann ◽  
...  
2019 ◽  
Vol 374 (1785) ◽  
pp. 20190277 ◽  
Author(s):  
Edgar T. Walters

Chronic pain is considered maladaptive by clinicians because it provides no apparent protective or recuperative benefits. Similarly, evolutionary speculations have assumed that chronic pain represents maladaptive or evolutionarily neutral dysregulation of acute pain mechanisms. By contrast, the present hypothesis proposes that chronic pain can be driven by mechanisms that evolved to reduce increased vulnerability to attack from predators and aggressive conspecifics, which often target prey showing physical impairment after severe injury. Ongoing pain and anxiety persisting long after severe injury continue to enhance vigilance and behavioural caution, decreasing the heightened vulnerability to attack that results from motor impairment and disfigurement, thereby increasing survival and reproduction (fitness). This hypothesis is supported by evidence of animals surviving and reproducing after traumatic amputations, and by complex specializations that enable primary nociceptors to detect local and systemic signs of injury and inflammation, and to maintain low-frequency discharge that can promote ongoing pain indefinitely. Ongoing activity in nociceptors involves intricate electrophysiological and anatomical specializations, including inducible alterations in the expression of ion channels and receptors that produce persistent hyperexcitability and hypersensitivity to chemical signals of injury. Clinically maladaptive chronic pain may sometimes result from the recruitment of this powerful evolutionary adaptation to severe bodily injury. This article is part of the Theo Murphy meeting issue ‘Evolution of mechanisms and behaviour important for pain’.


2021 ◽  
Vol 11 (5) ◽  
pp. 639
Author(s):  
David Bergeron ◽  
Sami Obaid ◽  
Marie-Pierre Fournier-Gosselin ◽  
Alain Bouthillier ◽  
Dang Khoa Nguyen

Introduction: To date, clinical trials of deep brain stimulation (DBS) for refractory chronic pain have yielded unsatisfying results. Recent evidence suggests that the posterior insula may represent a promising DBS target for this indication. Methods: We present a narrative review highlighting the theoretical basis of posterior insula DBS in patients with chronic pain. Results: Neuroanatomical studies identified the posterior insula as an important cortical relay center for pain and interoception. Intracranial neuronal recordings showed that the earliest response to painful laser stimulation occurs in the posterior insula. The posterior insula is one of the only regions in the brain whose low-frequency electrical stimulation can elicit painful sensations. Most chronic pain syndromes, such as fibromyalgia, had abnormal functional connectivity of the posterior insula on functional imaging. Finally, preliminary results indicated that high-frequency electrical stimulation of the posterior insula can acutely increase pain thresholds. Conclusion: In light of the converging evidence from neuroanatomical, brain lesion, neuroimaging, and intracranial recording and stimulation as well as non-invasive stimulation studies, it appears that the insula is a critical hub for central integration and processing of painful stimuli, whose high-frequency electrical stimulation has the potential to relieve patients from the sensory and affective burden of chronic pain.


1997 ◽  
Vol 102 (C11) ◽  
pp. 25005-25020 ◽  
Author(s):  
M. N. Tsimplis ◽  
A. F. Velegrakis ◽  
A. Theocharis ◽  
M. B. Collins

1996 ◽  
Vol 32 (7) ◽  
pp. 605 ◽  
Author(s):  
K. Tanno ◽  
O. Ishizuka ◽  
Z. Tang

2003 ◽  
Vol 17 (2-3) ◽  
pp. 249-253 ◽  
Author(s):  
V. Samuilov ◽  
T. Veselova ◽  
A. Cenys ◽  
K.G. Kyritsi ◽  
A.N. Anagnostopoulos ◽  
...  

2015 ◽  
Vol 30 (8) ◽  
pp. 4336-4348 ◽  
Author(s):  
Sinan Li ◽  
Guo-Rong Zhu ◽  
Siew-Chong Tan ◽  
S. Y. Hui

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