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1,3-dipropyl-8-cyclopentylxanthine and Allodynia

1,3-dipropyl-8-cyclopentylxanthine has been researched along with Allodynia in 17 studies

DPCPX : An oxopurine that is 7H-xanthine substituted at positions 1 and 3 by propyl groups and at position 8 by a cyclohexyl group.

Research Excerpts

ExcerptRelevanceReference
" Additionally, incarvillateine attenuated mechanical allodynia induced by spared nerve injury or paclitaxel, whereas normal mechanical sensation was not affected."3.81Antinociceptive effects of incarvillateine, a monoterpene alkaloid from Incarvillea sinensis, and possible involvement of the adenosine system. ( Gong, ZH; Huang, B; Jia, YX; Su, RB; Wang, ML; Wang, ZT; Yi, SP; Yu, G; Zhang, FY, 2015)
"This study investigated the involvement of the adenosinergic system in antiallodynia induced by exercise in an animal model of complex regional pain syndrome type I (CRPS-I)."3.79High-intensity swimming exercise reduces neuropathic pain in an animal model of complex regional pain syndrome type I: evidence for a role of the adenosinergic system. ( Martins, DF; Mazzardo-Martins, L; Piovezan, AP; Santos, AR; Soldi, F; Stramosk, J, 2013)
"This study was undertaken in order to investigate the effect of chronic treatment with 5′-chloro-5′-deoxy-(±)-ENBA, a potent and highly selective agonist of human adenosine A(1) receptor, on thermal hyperalgesia and mechanical allodynia in a mouse model of neuropathic pain, the Spared Nerve Injury (SNI) of the sciatic nerve."3.785'-Chloro-5'-deoxy-(±)-ENBA, a potent and selective adenosine A(1) receptor agonist, alleviates neuropathic pain in mice through functional glial and microglial changes without affecting motor or cardiovascular functions. ( Cappellacci, L; de Novellis, V; Franchetti, P; Gatta, L; Giordano, C; Grifantini, M; Guida, F; Luongo, L; Maione, S; Petrelli, R; Vita, P, 2012)
"It is associated with allodynia and hyperalgesia."1.48Neurobiological mechanisms of antiallodynic effect of transcranial direct current stimulation (tDCS) in a mice model of neuropathic pain. ( Caumo, W; Dos Santos, ARS; Martins, DF; Martins, TC; Medeiros, LF; Nucci-Martins, C; Siteneski, A; Souza, A; Torres, ILS, 2018)
"In the primed paw AMP hyperalgesia was dependent on conversion to adenosine, being prevented by ecto-5'nucleotidase inhibitor α,β-methyleneadenosine 5'-diphosphate sodium salt and A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine."1.46Regulation of Expression of Hyperalgesic Priming by Estrogen Receptor α in the Rat. ( Araldi, D; Ferrari, LF; Levine, JD, 2017)
"The adenosinergic system was assessed by systemic (intraperitoneal), central (intrathecal), and peripheral (intraplantar) administration of caffeine."1.39Ankle joint mobilization affects postoperative pain through peripheral and central adenosine A1 receptors. ( Cidral-Filho, FJ; Martins, DF; Mazzardo-Martins, L; Santos, AR; Stramosk, J, 2013)
"To evaluate the effect of adenosine on thermal hyperalgesia after spinal cord injury (SCI)."1.36Adenosine A1 receptor agonists reduce hyperalgesia after spinal cord injury in rats. ( Horiuchi, H; Morino, T; Ogata, T; Yamamoto, H, 2010)

Research

Studies (17)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's7 (41.18)29.6817
2010's9 (52.94)24.3611
2020's1 (5.88)2.80

Authors

AuthorsStudies
Liu, H1
Altenbach, RJ1
Carr, TL1
Chandran, P1
Hsieh, GC1
Lewis, LG1
Manelli, AM1
Milicic, I1
Marsh, KC1
Miller, TR1
Strakhova, MI1
Vortherms, TA1
Wakefield, BD1
Wetter, JM1
Witte, DG1
Honore, P1
Esbenshade, TA1
Brioni, JD1
Cowart, MD1
Xie, AX1
Madayag, A1
Minton, SK1
McCarthy, KD1
Malykhina, AP1
Souza, A1
Martins, DF3
Medeiros, LF1
Nucci-Martins, C1
Martins, TC1
Siteneski, A1
Caumo, W1
Dos Santos, ARS1
Torres, ILS1
Imlach, WL1
Bhola, RF1
May, LT1
Christopoulos, A1
Christie, MJ1
Wang, ML1
Yu, G1
Yi, SP1
Zhang, FY1
Wang, ZT1
Huang, B1
Su, RB1
Jia, YX1
Gong, ZH1
Ferrari, LF1
Araldi, D1
Levine, JD1
Horiuchi, H1
Ogata, T1
Morino, T1
Yamamoto, H1
Lima, FO1
Souza, GR1
Verri, WA1
Parada, CA1
Ferreira, SH1
Cunha, FQ1
Cunha, TM1
Mazzardo-Martins, L2
Cidral-Filho, FJ1
Stramosk, J2
Santos, AR2
Luongo, L1
Petrelli, R1
Gatta, L1
Giordano, C1
Guida, F1
Vita, P1
Franchetti, P1
Grifantini, M1
de Novellis, V1
Cappellacci, L1
Maione, S1
Soldi, F1
Piovezan, AP1
da Silva Torres, IL1
Bonan, CD1
Crema, L1
De Leon Nunes, M1
Battastini, AM1
Sarkis, JJ1
Dalmaz, C1
Ferreira, MB1
Wu, WP1
Hao, JX1
Halldner, L1
Lövdahl, C1
DeLander, GE1
Wiesenfeld-Hallin, Z1
Fredholm, BB1
Xu, XJ1
Vuckovic, S1
Tomic, M1
Stepanovic-Petrovic, R1
Ugresic, N2
Prostran, M1
Boskovic, B2
Tomić, MA1
Vucković, SM1
Stepanović-Petrović, RM1
Prostran, MS1
Savegnago, L1
Jesse, CR1
Nogueira, CW1
Yasuda, T1
Okamoto, K1
Iwamoto, T1
Miki, S1
Yoshinaga, N1
Sato, S1
Noguchi, K1
Senba, E1

Other Studies

17 other studies available for 1,3-dipropyl-8-cyclopentylxanthine and Allodynia

ArticleYear
cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11a-octahydrobenzofuro[2,3-h]quinazolin-2-amine (A-987306), a new histamine H4R antagonist that blocks pain responses against carrageenan-induced hyperalgesia.
    Journal of medicinal chemistry, 2008, Nov-27, Volume: 51, Issue:22

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Benzofurans; Carrageenan; Disease Models, Animal;

2008
Sensory satellite glial Gq-GPCR activation alleviates inflammatory pain via peripheral adenosine 1 receptor activation.
    Scientific reports, 2020, 08-25, Volume: 10, Issue:1

    Topics: Animals; Benzilates; Clozapine; Freund's Adjuvant; Genes, Synthetic; GTP-Binding Protein alpha Subun

2020
Neurobiological mechanisms of antiallodynic effect of transcranial direct current stimulation (tDCS) in a mice model of neuropathic pain.
    Brain research, 2018, 03-01, Volume: 1682

    Topics: Adenosine A1 Receptor Antagonists; Animals; Caffeine; Central Nervous System Stimulants; Disease Mod

2018
A Positive Allosteric Modulator of the Adenosine A1 Receptor Selectively Inhibits Primary Afferent Synaptic Transmission in a Neuropathic Pain Model.
    Molecular pharmacology, 2015, Volume: 88, Issue:3

    Topics: Adenosine A1 Receptor Agonists; Allosteric Regulation; Animals; Excitatory Postsynaptic Potentials;

2015
Antinociceptive effects of incarvillateine, a monoterpene alkaloid from Incarvillea sinensis, and possible involvement of the adenosine system.
    Scientific reports, 2015, Nov-03, Volume: 5

    Topics: Adenosine; Alkaloids; Analgesics; Animals; Antineoplastic Agents, Phytogenic; Bignoniaceae; Disease

2015
Regulation of Expression of Hyperalgesic Priming by Estrogen Receptor α in the Rat.
    The journal of pain, 2017, Volume: 18, Issue:5

    Topics: 5'-Nucleotidase; Adenosine; Adenosine A1 Receptor Antagonists; Adenosine Monophosphate; Animals; Chr

2017
Adenosine A1 receptor agonists reduce hyperalgesia after spinal cord injury in rats.
    Spinal cord, 2010, Volume: 48, Issue:9

    Topics: Adenosine; Adenosine A1 Receptor Agonists; Adenosine A1 Receptor Antagonists; Adenosine A2 Receptor

2010
Direct blockade of inflammatory hypernociception by peripheral A1 adenosine receptors: involvement of the NO/cGMP/PKG/KATP signaling pathway.
    Pain, 2010, Volume: 151, Issue:2

    Topics: Adenosine A1 Receptor Antagonists; Analysis of Variance; Animals; Carrageenan; Cyclic GMP; Cyclic GM

2010
Ankle joint mobilization affects postoperative pain through peripheral and central adenosine A1 receptors.
    Physical therapy, 2013, Volume: 93, Issue:3

    Topics: Adenosine; Analysis of Variance; Animals; Ankle Joint; Caffeine; Clonidine; Disease Models, Animal;

2013
5'-Chloro-5'-deoxy-(±)-ENBA, a potent and selective adenosine A(1) receptor agonist, alleviates neuropathic pain in mice through functional glial and microglial changes without affecting motor or cardiovascular functions.
    Molecules (Basel, Switzerland), 2012, Nov-22, Volume: 17, Issue:12

    Topics: Adenosine; Adenosine A1 Receptor Agonists; Animals; Cardiovascular System; Humans; Hyperalgesia; Mic

2012
High-intensity swimming exercise reduces neuropathic pain in an animal model of complex regional pain syndrome type I: evidence for a role of the adenosinergic system.
    Neuroscience, 2013, Mar-27, Volume: 234

    Topics: Adenine; Adenosine; Adenosine A1 Receptor Antagonists; Adenosine A2 Receptor Antagonists; Adenosine

2013
Effect of drugs active at adenosine receptors upon chronic stress-induced hyperalgesia in rats.
    European journal of pharmacology, 2003, Nov-28, Volume: 481, Issue:2-3

    Topics: Adenosine; Animals; Chronic Disease; Hyperalgesia; Male; Pain Measurement; Purinergic P1 Receptor Ag

2003
Increased nociceptive response in mice lacking the adenosine A1 receptor.
    Pain, 2005, Volume: 113, Issue:3

    Topics: Adenosine A1 Receptor Agonists; Adenosine A1 Receptor Antagonists; Analgesics, Opioid; Analysis of V

2005
Peripheral antinociception by carbamazepine in an inflammatory mechanical hyperalgesia model in the rat: a new target for carbamazepine?
    Journal of pharmacological sciences, 2006, Volume: 100, Issue:4

    Topics: Analgesics; Animals; Caffeine; Carbamazepine; Concanavalin A; Disease Models, Animal; Dose-Response

2006
Peripheral anti-hyperalgesia by oxcarbazepine: involvement of adenosine A1 receptors.
    Die Pharmazie, 2006, Volume: 61, Issue:6

    Topics: Adenosine A1 Receptor Agonists; Adenosine A1 Receptor Antagonists; Animals; Anticonvulsants; Caffein

2006
Caffeine and a selective adenosine A(2B) receptor antagonist but not imidazoline receptor antagonists modulate antinociception induced by diphenyl diselenide in mice.
    Neuroscience letters, 2008, May-09, Volume: 436, Issue:2

    Topics: Adrenergic alpha-Antagonists; Animals; Behavior, Animal; Benzene Derivatives; Benzofurans; Caffeine;

2008
A novel analgesic compound OT-7100 attenuates nociceptive responses in animal models of inflammatory and neuropathic hyperalgesia: a possible involvement of adenosinergic anti-nociception.
    Japanese journal of pharmacology, 2001, Volume: 87, Issue:3

    Topics: Adenosine; Analgesics, Non-Narcotic; Animals; Disease Models, Animal; Guinea Pigs; Hyperalgesia; Imm

2001