Page last updated: 2024-10-21

1,3-dipropyl-8-cyclopentylxanthine and Visceral Pain

1,3-dipropyl-8-cyclopentylxanthine has been researched along with Visceral Pain in 1 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.

Visceral Pain: Pain originating from internal organs (VISCERA) associated with autonomic phenomena (PALLOR; SWEATING; NAUSEA; and VOMITING). It often becomes a REFERRED PAIN.

Research Excerpts

ExcerptRelevanceReference
" Adenosine signaling is capable of inducing an antinociceptive action against somatic pain; however, the association between changes in the adenosinergic system and visceral pain perception has not been investigated."3.83Adenosine A1 receptors mediate the intracisternal injection of orexin-induced antinociceptive action against colonic distension in conscious rats. ( Kumei, S; Miyagishi, S; Nozu, T; Ohhira, M; Okumura, T; Takakusaki, K, 2016)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Okumura, T1
Nozu, T1
Kumei, S1
Takakusaki, K1
Miyagishi, S1
Ohhira, M1

Other Studies

1 other study available for 1,3-dipropyl-8-cyclopentylxanthine and Visceral Pain

ArticleYear
Adenosine A1 receptors mediate the intracisternal injection of orexin-induced antinociceptive action against colonic distension in conscious rats.
    Journal of the neurological sciences, 2016, Mar-15, Volume: 362

    Topics: Adenosine; Adenosine A1 Receptor Antagonists; Analgesics; Animals; Colon; Consciousness; Disease Mod

2016