4.5 Article

Ginger metabolites and metabolite-inspired synthetic products modulate intracellular calcium and relax airway smooth muscle

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajplung.00271.2021

Keywords

airway smooth muscle relaxation; inositol trisphosphate; intracellular calcium; phospholipase C; 6-Shogaol metabolites

Funding

  1. National Institutes of Health (NIH) National Heart, Lung, and Blood Institute [HL122340]
  2. National Institute of General Medical Sciences [GM065281, T32GM008464]
  3. Stony Wold-Herbert Fund Inc.
  4. Virginia Apgar Scholars Program at the Department of Anesthesiology, Columbia University

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The study shows that metabolites and synthetic derivatives of the primary active component, 6-shogaol, in ginger can inhibit airway constriction and enhance relaxation, offering potential therapeutic options for asthma and other bronchoconstrictive diseases. This suggests that natural metabolites could inspire the development of novel therapeutics in the treatment of respiratory conditions.
Asthma affects millions of people worldwide and its prevalence is increasing. It is characterized by chronic airway inflammation, airway remodeling, and pathologic bronchoconstriction, and it poses a continuous treatment challenge with very few new therapeutics available. Thus, many asthmatics turn to plant-based complementary products, including ginger, for better symptom control, indicating an unmet need for novel therapies. Previously, we demonstrated that 6-shogaol (65), the primary bioactive component of ginger, relaxes human airway smooth muscle (hASM) likely by inhibition of phosphodiesterases (PDEs) in the beta-adrenergic (cyclic nucleotide PDEs), and muscarinic (phospholipase C, PLC) receptor pathways. However, oral 65 is extensively metabolized and it is unknown if the resulting metabolites remain bioactive. Here, we screened all the known human metabolites of 6S and several metabolite-based synthetic derivatives to better understand their mechanism of action and structure-function relationships. We demonstrate that several metabolites and metabolite-based synthetic derivatives are able to prevent Gq- coupled stimulation of intracellular calcium [Ca2+], and inositol trisphosphate (IP3) synthesis by inhibiting PLC, similar to the parent compound 6S. We also show that these compounds prevent recontraction of ASM after beta-agonist relaxation likely by inhibiting PDEs. Furthermore, they potentiate isoproterenol-induced relaxation. Importantly, moving beyond cell-based assays, metabolites also retain the functional ability to relax Gq-coupled-contractions in upper (human) and lower (murine) airways. The current study indicates that, although oral ginger may be metabolized rapidly, it retains physiological activity through its metabolites. Moreover, we are able to use naturally occurring metabolites as inspiration to develop novel therapeutics for brochoconstrictive diseases.

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