Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2007;69(1):70-82.
doi: 10.1016/j.mehy.2006.11.028. Epub 2007 Jan 19.

The biochemical origin of pain--proposing a new law of pain: the origin of all pain is inflammation and the inflammatory response. Part 1 of 3--a unifying law of pain

Affiliations

The biochemical origin of pain--proposing a new law of pain: the origin of all pain is inflammation and the inflammatory response. Part 1 of 3--a unifying law of pain

Sota Omoigui. Med Hypotheses. 2007.

Abstract

We are proposing a unifying theory or law of pain, which states: the origin of all pain is inflammation and the inflammatory response. The biochemical mediators of inflammation include cytokines, neuropeptides, growth factors and neurotransmitters. Irrespective of the type of pain whether it is acute or chronic pain, peripheral or central pain, nociceptive or neuropathic pain, the underlying origin is inflammation and the inflammatory response. Activation of pain receptors, transmission and modulation of pain signals, neuro plasticity and central sensitization are all one continuum of inflammation and the inflammatory response. Irrespective of the characteristic of the pain, whether it is sharp, dull, aching, burning, stabbing, numbing or tingling, all pain arise from inflammation and the inflammatory response. We are proposing a re-classification and treatment of pain syndromes based upon their inflammatory profile. Treatment of pain syndromes should be based on these principles: 1. Determination of the inflammatory profile of the pain syndrome; 2. Inhibition or suppression of production of the appropriate inflammatory mediators, e.g. with inflammatory mediator blockers or surgical intervention where appropriate; 3. Inhibition or suppression of neuronal afferent and efferent (motor) transmission, e.g. with anti-seizure drugs or local anesthetic blocks; 4. Modulation of neuronal transmission, e.g. with opioid medication. At the L.A. Pain Clinic, we have successfully treated a variety of pain syndromes by utilizing these principles. This theory of the biochemical origin of pain is compatible with, inclusive of, and unifies existing theories and knowledge of the mechanism of pain including the gate control theory, and theories of pre-emptive analgesia, windup and central sensitization.

PubMed Disclaimer

Conflict of interest statement

The paper is not under consideration elsewhere and none of the paper's contents have been previously published. All authors have read and approved the manuscript.

Work was done at the L.A. Pain Clinic. The study was not supported by any grant. There is no conflict of interest.

References

    1. Sherrington CS. The Integrative Action of the Nervous System. New Haven, Connecticut: Yale Univ. Press; 1906.
    1. Livingstone WK. Pain Mechanisms. New York: Macmillan; 1943.
    1. Online Exhibit. Pain and Suffering in History–Narratives of Science, Medicine and Culture. John C. Liebeskind History of Pain Collection at the Louise M. Darling Biomedical Library, UCLA.

    1. Melzack R, Wall PD. Pain mechanisms: a new theory. Science. 1965 Nov 19;150(699):971–979. - PubMed
    1. Melzack R. Pain: past, present and future. Can J Exp Psychol. 1993 Dec;47(4):615–629. - PubMed

Substances