Introduction:What they say:
A recent study from Institute of Neurobiology, Institutes of Brain Science and State Key Laboratory of Medical Neurobiology, Collaborative Innovation Center for Brain Science, Fudan University, Shanghai, China; and Department of Neurobiology, Duke University Medical Center, Durham, North Carolina, US shows that “PD-L1 inhibits acute and chronic pain by suppressing nociceptive neuron activity via PD-1.” This study was published, in the 22 May 2017 issue of Nature Neuroscience (one of the best journals in Neurobiology with an impact factor of 16.724+), by Prof Ru-Rong Ji, Chen G and others.
What we say:
On the foundation of this interesting finding, Dr L Boominathan PhD, the Director-cum-chief Scientist of GBMD, reports that: Solving a century-old puzzle as to how Sesame oil functions as a pain reliever: Mechanistic insights into how Sesame oil-derived compounds function as pain medications: A pharmaceutical mixture encompassing Sesamin and Sesamol (SAS), derived from Sesame seed or oil, increases the expression of PD-L1, decreases the expression of Cox-2, attenuates acutes and chronic pain, and suppresses mechanical and thermal hypersensitivity and inhibits nociceptive neuron excitability, via up-regulation of its target gene
What is known?
It has recently been shown that blocking PD-1 with antibodies one could make tumors shrink. This work, relating to Cancer immunotherapy, has been chosen as Science’s breakthrough of the year. However, the work published recently, which is described below, may highlight the caveat in such an approach, as blocking PD-L1 may promote spontaneous pain and allodynia in cancer-bearing mice.
Prof. Ji has shown recently that: (1) Programmed cell death ligand-1 (PD-L1), produced by melanoma and normal neural tissues, inhibits acute and chronic pain; (2) injection of PD-L1 alleviates pain, and thereby functions as an analgesic agent; (3) Neutralization of PD-L1 or Block of PD1 promotes mechanical allodynia (hypersensitivity to pain); (4) PD1 null mice suffers from thermal and mechanical hypersensitivity; (5) PD-L1 promotes phosphorylation of SHP-1 and inhibits Sodium channels via PD-1 activation; and (6) PD-L1 inhibits nociceptive neuron excitability in dorsal root ganglion and thereby functions as a neuromodulator, suggesting that increasing the expression or the level of PD-L1/PD1 may alleviate pain and thermal and mechanical hypersensitivity.
From research findings to therapeutic opportunity:
Sesame oil is used in India and in other asian countries, in ayurvedic medicine, for centuries, however, the mechanistic basis of its therapeutic effect, in the treatment of pain, remains largely obscure for centuries. This study provides, for the first time, mechanistic insights into how commonly used sesame oil and its constituents, such as Sesamin, and sesamol, may attenuate pain and trauma.
A therapeutic mix encompassing Sesamin and Sesamol, by increasing the expression of its target genes, it increases PD-L1 and decreases Cox-2 (Cyclooxygenase-2) levels (fig. 1). Thereby, it: (a) inhibits acute and chronic pain and trauma; (b) alleviates thermal and mechanical hypersensitivity; (c) activates signal transduction cascade downstream of PD-1 receptor; (c) phosphorylates SHP-1; (d) inhibits sodium channels and nociceptive neuron excitability (Fig 2-4). Thus, a pharmacological mixture encompassing Sesamin and Sesamol (SAS) or their analogs, either alone or in combination with other drugs, can be used to treat acute and chronic pain and trauma.
Given the mechanistic basis as to how sesame oil and its components (fig.1) aid in attenuating or decreasing or alleviating short- and long-term pain and trauma, physicians/orthopedicians/pain therapists may consider encouraging their patients to undergo Sesame oil-based massage therapy regularly.
Together, this study, for the first time, paves not only a way to identify new analgesic drugs from sesame oil or seeds, but also suggests as to how Sesame oil-based massage therapy may function as an adjuvant therapy, for patients suffering from short- and long-term pain and trauma (Figure 2-4).
Details of the research findings:
Idea Proposed/Formulated (with experimental evidence) by: Dr L Boominathan Ph.D.
Terms & Conditions apply http://genomediscovery.org/registration/terms-and-conditions/
Amount: $1, 500#
Undisclosed mechanistic information: How does a pharmaceutical mixture encompassing Sesamin and Sesamol (SAS) increase the expression of PD-L1?
# Research cooperation
Citation: Boominathan, L., Solving a century-old puzzle as to how Sesame oil functions as a pain reliever: Mechanistic insights into how Sesame oil-derived compounds function as pain medications: A pharmaceutical mixture encompassing Sesamin and Sesamol (SAS), derived from Sesame seed or oil, increases the expression of PD-L1, decreases the expression of Cox-2, attenuates acutes and chronic pain, and suppresses mechanical and thermal hypersensitivity and inhibits nociceptive neuron excitability, via up-regulation of its target gene, 17/June/2019, 12.58 pm, Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org
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