Table 3.
Summary of the pharmacological benefits and its mechanism of action.
Health beneficial | Mechanism of action | Reference |
---|---|---|
Analgesic effect | vlPAG leads to TRPV1 activation which helps to release glutamate into RVM and induce the activation of OFF-cells and reduced the pain pathway | [213] |
Antioxidant activity | Phytochemical components - phenolics and flavonoids inhibits radiation-induced biochemical alterations including protein oxidation and lipid peroxidation | [214] |
Antimicrobial activity | Disrupt the peptidoglycan structure due to lipid-lipid interactions providing liquidity in the cell wall and also induced the osmotic stress, responsible for gene expression inhibition | [215] |
Gastro protective effects | Due to activation of TRPV1 at gastric sensory neurons – stimulates the release of CGRP and NO | [216] |
Cancer prevention | ROS generation, increased in intracellular Ca2+, activation of transcription factors (NF-κB and STATs), disruption of mitochondrial membrane transition potential, and AMP-dependent kinase pathway | [217] |
Cardiovascular benefits | Due to presence of TRPV1 in platelets provoked Ca2+ release from intracellular platelet contributing to ADP and thrombin induced platelet activation | [218] |
Anti-obesity effect | Lowered fasting glucose, insulin, leptin level and also lower the tumor necrosis factor-alpha (TNFα), monocyte chemo-attractant protein-1 MCP-1), interleukin (IL)-6 mRNAs in adipose tissue and liver. | [219] |
Inflammation curing | Inhibits the NF-κB phosphorylation which then reduces downstream IL-6 and TNFα target. | [220] |
vlPAG: ventrolateral periaqueductal gray; TRPV1: transient receptor potential vanilloid 1; RVM: rostroventral medulla; CGRP: calcitonin gene-related peptides; NO: nitric oxide; ROS: reactive oxygen species; NF-κB: nuclear factor κ; STATs: signal transducers and activators of transcription; AMP: Adenosine monophosphate; TNFα: tumor necrosis factor-alpha; MCP-1: monocyte chemo-attractant protein-1; IL-6: interleukin-6.