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clomipramine and Alloxan Diabetes

clomipramine has been researched along with Alloxan Diabetes in 7 studies

Clomipramine: A tricyclic antidepressant similar to IMIPRAMINE that selectively inhibits the uptake of serotonin in the brain. It is readily absorbed from the gastrointestinal tract and demethylated in the liver to form its primary active metabolite, desmethylclomipramine.
clomipramine : A dibenzoazepine that is 10,11-dihydro-5H-dibenzo[b,f]azepine which is substituted by chlorine at position 3 and in which the hydrogen attached to the nitrogen is replaced by a 3-(dimethylamino)propyl group. One of the more sedating tricyclic antidepressants, it is used as the hydrochloride salt for the treatment of depression as well as obsessive-compulsive disorder and phobias.

Research Excerpts

ExcerptRelevanceReference
"Corticosterone levels were increased in the untreated STZ group; SMV and clomipramine significantly decreased corticosterone levels in the STZ groups, but had no effect on the CTR groups."1.42Antidepressant-like effect of simvastatin in diabetic rats. ( ElBatsh, MM, 2015)
"Abolition of mechanical hyperalgesia was observed in mononeuropathic rats after five injections of clomipramine (5 mg·kg(-1) , s."1.37Evidence for a differential opioidergic involvement in the analgesic effect of antidepressants: prediction for efficacy in animal models of neuropathic pain? ( Courteix, C; Eschalier, A; Fialip, J; Libert, F; Loiodice, S; Privat, AM; Wattiez, AS, 2011)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's1 (14.29)18.2507
2000's1 (14.29)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Suehiro, K1
Funao, T1
Fujimoto, Y1
Yamada, T1
Mori, T1
Nishikawa, K1
ElBatsh, MM1
Wattiez, AS1
Libert, F1
Privat, AM1
Loiodice, S1
Fialip, J2
Eschalier, A2
Courteix, C2
Coudoré-Civiale, MA1
Boucher, M1
Méen, M1
Ardid, D1
Massol, J3
Martin, P3
Chatelain, F2
Puech, AJ3
Belon, JP1
Soubrié, P2

Other Studies

7 other studies available for clomipramine and Alloxan Diabetes

ArticleYear
Relationship between noradrenaline release in the locus coeruleus and antiallodynic efficacy of analgesics in rats with painful diabetic neuropathy.
    Life sciences, 2013, Jun-21, Volume: 92, Issue:23

    Topics: Adrenergic Neurons; Analgesics; Animals; Clomipramine; Diabetes Mellitus, Experimental; Diabetic Neu

2013
Antidepressant-like effect of simvastatin in diabetic rats.
    Canadian journal of physiology and pharmacology, 2015, Volume: 93, Issue:8

    Topics: Animals; Antidepressive Agents; Behavior, Animal; Clomipramine; Corticosterone; Depression; Diabetes

2015
Evidence for a differential opioidergic involvement in the analgesic effect of antidepressants: prediction for efficacy in animal models of neuropathic pain?
    British journal of pharmacology, 2011, Volume: 163, Issue:4

    Topics: Analgesics; Animals; Antidepressive Agents; Clomipramine; Cyclopropanes; Diabetes Mellitus, Experime

2011
Potentiation of morphine and clomipramine analgesia by cholecystokinin -B antagonist CI-988 in diabetic rats.
    Neuroscience letters, 2000, May-26, Volume: 286, Issue:1

    Topics: Analgesia; Analgesics, Opioid; Animals; Anti-Anxiety Agents; Antidepressive Agents, Tricyclic; Clomi

2000
Tricyclic antidepressants, thyroid function, and their relationship with the behavioral responses in rats.
    Biological psychiatry, 1990, Dec-01, Volume: 28, Issue:11

    Topics: Animals; Antidepressive Agents, Tricyclic; Arousal; Avoidance Learning; Clomipramine; Conditioning,

1990
Helpless behavior (escape deficits) in streptozotocin-diabetic rats: resistance to antidepressant drugs.
    Psychoneuroendocrinology, 1989, Volume: 14, Issue:1-2

    Topics: Animals; Antidepressive Agents; Brain; Clenbuterol; Clomipramine; Conditioning, Operant; Desipramine

1989
Impaired response of experimental diabetic mice to tricyclics: a possible beta-adrenergic mechanism.
    Pharmacology, biochemistry, and behavior, 1988, Volume: 31, Issue:4

    Topics: Animals; Clenbuterol; Clomipramine; Desipramine; Diabetes Mellitus, Experimental; Dose-Response Rela

1988