capsaicin has been researched along with n-palmitoyl-vanillamide in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (83.33) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| De Chiaro, M; de Novellis, V; De Petrocellis, L; Di Marzo, V; Guida, F; Maione, S; Moriello, AS; Piscitelli, F | 1 |
| Comelli, F; Costa, B; D'Agostino, B; de Novellis, V; De Petrocellis, L; Di Marzo, V; Gatta, L; Guida, F; Luongo, L; Maione, S; Matteis, M; Sullo, N | 1 |
| Bellini, G; Giordano, C; Guida, F; Luongo, L; Maione, S; Manzo, I; Nobili, B; Papale, F; Rossi, F; Rosso, F; Torella, M; Tortora, C | 1 |
| Aguilar-Martínez, I; Alamilla, J; Álvarez-Cervera, FJ; Castro-Sánchez, LA; Dagnino-Acosta, A; Góngora-Alfaro, JL; Moreno-Galindo, EG; Navarro-Polanco, RA; Pérez-Burgos, A; Reyes-Mendez, ME; Vázquez-Jiménez, C | 1 |
| Adams, DJ; Finol-Urdaneta, RK; McArthur, JR | 1 |
| Di Marzo, V; Fichna, J; Storr, M; Szymaszkiewicz, A; Wasilewski, A; Włodarczyk, J; Zielińska, M | 1 |
6 other study(ies) available for capsaicin and n-palmitoyl-vanillamide
| Article | Year |
|---|---|
N-palmitoyl-vanillamide (palvanil) is a non-pungent analogue of capsaicin with stronger desensitizing capability against the TRPV1 receptor and anti-hyperalgesic activity.
Topics: Administration, Topical; Analgesics; Animals; Arachidonic Acids; Calcium; Capsaicin; Cell Line; Endocannabinoids; Eye; Humans; Male; Mice; Pain; Polyunsaturated Alkamides; TRPV Cation Channels | 2011 |
Palvanil, a non-pungent capsaicin analogue, inhibits inflammatory and neuropathic pain with little effects on bronchopulmonary function and body temperature.
Topics: Analgesics; Animals; Body Temperature; Bronchoconstriction; Capsaicin; Edema; Female; Hyperalgesia; Hypothermia; Inflammation; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Neuralgia; Pain Measurement; Respiratory System; Sciatic Nerve; TRPV Cation Channels | 2012 |
The genetic ablation or pharmacological inhibition of TRPV1 signalling is beneficial for the restoration of quiescent osteoclast activity in ovariectomized mice.
Topics: Animals; Bone Density; Bone Density Conservation Agents; Bone Remodeling; Capsaicin; Cells, Cultured; Disease Models, Animal; Dose-Response Relationship, Drug; Female; Humans; Mice, Inbred C57BL; Mice, Knockout; Osteoclasts; Osteoporosis, Postmenopausal; Ovariectomy; Receptor Cross-Talk; Receptor, Cannabinoid, CB2; Signal Transduction; TRPV Cation Channels | 2014 |
Capsaicin produces antidepressant-like effects in the forced swimming test and enhances the response of a sub-effective dose of amitriptyline in rats.
Topics: Amitriptyline; Animals; Antidepressive Agents; Anxiety; Capsaicin; Depressive Disorder; Dose-Response Relationship, Drug; Male; Muscle Contraction; Random Allocation; Rats, Wistar; Swimming; TRPV Cation Channels | 2018 |
Analgesic transient receptor potential vanilloid-1-active compounds inhibit native and recombinant T-type calcium channels.
Topics: Analgesics; Animals; Calcium Channel Blockers; Calcium Channels, T-Type; Capsaicin; Diterpenes; Ganglia, Spinal; HEK293 Cells; Humans; Neurons; Rats, Sprague-Dawley; TRPV Cation Channels | 2019 |
Desensitization of transient receptor potential vanilloid type-1 (TRPV1) channel as promising therapy of irritable bowel syndrome: characterization of the action of palvanil in the mouse gastrointestinal tract.
Topics: Abdominal Pain; Analgesics; Animals; Behavior, Animal; Capsaicin; Colon; Disease Models, Animal; Gastrointestinal Motility; In Vitro Techniques; Irritable Bowel Syndrome; Male; Mice, Inbred BALB C; Mustard Plant; Plant Oils; Time Factors; TRPV Cation Channels | 2020 |