Page last updated: 2024-08-23

substance p and tramadol

substance p has been researched along with tramadol in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Balzarini, P; Baratelli, E; Bianchi, M; Broggini, M; Ferrario, P; Panerai, AE; Sacerdote, P	1
Minami, K; Ogata, J; Uezono, Y; Yokoyama, T	1
Arizpe, HM; Clifford, JL; Fowler, M; Garza, TH; Loyd, DR; Novak, J; Petz, LN; Slater, TM	1

Trials

1 trial(s) available for substance p and tramadol

Article	Year
Effects of tramadol on synovial fluid concentrations of substance P and interleukin-6 in patients with knee osteoarthritis: comparison with paracetamol. International immunopharmacology, 2003, Volume: 3, Issue:13-14 Topics: Acetaminophen; Administration, Oral; Aged; Double-Blind Method; Female; Humans; Interleukin-6; Male; Middle Aged; Osteoarthritis, Knee; Pain; Pain Measurement; Prospective Studies; Substance P; Synovial Fluid; Time Factors; Tramadol	2003

Article

Year

Effects of tramadol on synovial fluid concentrations of substance P and interleukin-6 in patients with knee osteoarthritis: comparison with paracetamol.

International immunopharmacology, 2003, Volume: 3, Issue:13-14

Topics: Acetaminophen; Administration, Oral; Aged; Double-Blind Method; Female; Humans; Interleukin-6; Male; Middle Aged; Osteoarthritis, Knee; Pain; Pain Measurement; Prospective Studies; Substance P; Synovial Fluid; Time Factors; Tramadol

2003

Other Studies

2 other study(ies) available for substance p and tramadol

Article	Year
The tramadol metabolite O-desmethyl tramadol inhibits substance P-receptor functions expressed in Xenopus oocytes. Journal of pharmacological sciences, 2011, Volume: 115, Issue:3 Topics: Analgesics, Opioid; Animals; Chloride Channels; Indoles; Maleimides; Neurokinin-1 Receptor Antagonists; Oocytes; Protein Kinase Inhibitors; Receptors, Neurokinin-1; Substance P; Tramadol; Xenopus	2011
A rat model of full thickness thermal injury characterized by thermal hyperalgesia, mechanical allodynia, pronociceptive peptide release and tramadol analgesia. Burns : journal of the International Society for Burn Injuries, 2014, Volume: 40, Issue:4 Topics: Analgesics, Opioid; Animals; Behavior, Animal; Burns; Calcitonin Gene-Related Peptide; Disease Models, Animal; Hyperalgesia; Male; Morphine; Nociception; Nociceptive Pain; Pain; Rats; Rats, Sprague-Dawley; Spinal Cord; Substance P; Tramadol	2014

Article

Year

The tramadol metabolite O-desmethyl tramadol inhibits substance P-receptor functions expressed in Xenopus oocytes.

Journal of pharmacological sciences, 2011, Volume: 115, Issue:3

Topics: Analgesics, Opioid; Animals; Chloride Channels; Indoles; Maleimides; Neurokinin-1 Receptor Antagonists; Oocytes; Protein Kinase Inhibitors; Receptors, Neurokinin-1; Substance P; Tramadol; Xenopus

2011

A rat model of full thickness thermal injury characterized by thermal hyperalgesia, mechanical allodynia, pronociceptive peptide release and tramadol analgesia.

Burns : journal of the International Society for Burn Injuries, 2014, Volume: 40, Issue:4

Topics: Analgesics, Opioid; Animals; Behavior, Animal; Burns; Calcitonin Gene-Related Peptide; Disease Models, Animal; Hyperalgesia; Male; Morphine; Nociception; Nociceptive Pain; Pain; Rats; Rats, Sprague-Dawley; Spinal Cord; Substance P; Tramadol

2014