2016
DOI: 10.3892/ijmm.2016.2791
|View full text |Cite
|
Sign up to set email alerts
|

Effects of ginger and its pungent constituents on transient receptor potential channels

Abstract: Ginger extract is used as an analeptic in herbal medicine and has been reported to exert antioxidant effects. Transient receptor potential (TRP) canonical 5 (TRPC5), TRP cation channel, subfamily M, member 7 (TRPM7; melastatin 7), and TRP cation channel, subfamily A, member 1 (TRPA1; ankyrin 1) are non-selective cation channels that are modulated by reactive oxygen/nitrogen species (ROS/RNS) and subsequently control various cellular processes. The aim of this study was to evaluate whether ginger and its pungen… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
11
0

Year Published

2017
2017
2024
2024

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 20 publications
(11 citation statements)
references
References 61 publications
0
11
0
Order By: Relevance
“…Ginger is known for having more than 60 active compounds, broadly divided into volatile and nonvolatile compounds [ 6 ]. Volatile components include hydrocarbons, meanwhile rhizome from ginger contains nonvolatile pungent phenolic compounds like 6-gingerol, 6-shagol, 6-paradol, and zingerone [ 7 ] ( Figure 1 , Table 1 ).…”
Section: Introductionmentioning
confidence: 99%
“…Ginger is known for having more than 60 active compounds, broadly divided into volatile and nonvolatile compounds [ 6 ]. Volatile components include hydrocarbons, meanwhile rhizome from ginger contains nonvolatile pungent phenolic compounds like 6-gingerol, 6-shagol, 6-paradol, and zingerone [ 7 ] ( Figure 1 , Table 1 ).…”
Section: Introductionmentioning
confidence: 99%
“…The cis-C6 double bond in the polyenic chain of a-SOH is critical for TRPA1 activation and no structural specificity is required for TRPV1 activation (521). Alkylamides and 6-shogaol act on TRPA1 by covalent bonding, whereas none of these compounds activate TRPV1 through such interactions (391,681).…”
mentioning
confidence: 99%
“…The chemical activators group is divided in turn into two subgroups depending on the origin of the activator/modulator: exogenous and endogenous. Exogenous stimuli are capsaicin [ 38 ] and its antagonist capsazepine [ 39 ], resiniferatoxin (RTX) [ 37 , 40 ], bradykinin [ 41 ], yohimbine [ 42 ], ethanol [ 43 ], evodiamine [ 44 ], 17-β-estradiol [ 45 ], quinazoline [ 46 ], progesterone [ 47 ], numerous opioids [ 48 ], nicotine [ 49 ], hyaluronan [ 50 ], insulin [ 51 ], tinyatoxin [ 52 ], olvanil [ 53 ], acetylsalicylic acid [ 54 ], eugenol [ 55 ], sesquiterpenes [ 56 , 57 , 58 ], cannabidiol [ 59 ], prenylphenols [ 60 ], zingerone [ 61 ], shogaol [ 61 ], PPAHV [ 62 ], gingerol [ 63 ], numerous pharmacological antagonists [ 64 , 65 , 66 , 67 ], and peptide toxins from different species [ 4 , 68 ]. Endogenous activators comprise numerous compounds [ 1 ], such as the wide family derived from polyunsaturated fatty acids (PUFAs).…”
Section: Figurementioning
confidence: 99%