Results 181 to 190 of about 7,547 (235)
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CNS and Neurological Disorders - Drug Targets, 2021
BACKGROUND Over the last few years, the number of people suffering from sleeping disorders has increased significantly despite negative effects on cognition and an association with brain inflammation.
A. Maher +3 more
semanticscholar +1 more source
BACKGROUND Over the last few years, the number of people suffering from sleeping disorders has increased significantly despite negative effects on cognition and an association with brain inflammation.
A. Maher +3 more
semanticscholar +1 more source
HETEROCYCLES, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Meng‐Yang Chang +3 more
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AbstractFor Abstract see ChemInform Abstract in Full Text.
Meng‐Yang Chang +3 more
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Pharmacokinetics of (+)-rolipram and (?)-rolipram in healthy volunteers
European Journal of Clinical Pharmacology, 1990Plasma levels of S-(+)-rolipram and R-(-)-rolipram in six healthy male volunteers were measured by radioimmunoassay after intravenous injection of 0.1 mg and oral administration of 1.0 mg of the pure enantiomers. Following i.v. treatment, plasma levels of both isomers declined in three phases, with half-lives of 0.2 h, 0.6-0.9 h and 6-8 h.
W, Krause, G, Kühne, N, Sauerbrey
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Vesicle-Encapsulated Rolipram (PDE4 Inhibitor) and Its Anticancer Activity
ACS Applied Bio Materials, 2023Vesicular carriers of drugs are popular for specific targeting and delivery. The most popular vesicles among these are liposomes. However, they suffer from some inherent limitations. In this work, alternative vesicles with enhanced stability, i.e., niosomes and bilosomes have been prepared, characterized, and their delivery efficiency studied ...
Durga Mondal +6 more
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Rolipram reduces excitotoxic neuronal damage
Neuroreport, 2001Proinflammatory cytokines are supposed to be involved in the pathophysiology of neuronal damage following excitotoxic lesions. We examined the effect of rolipram, a TNF-alpha-inhibitor, on excitotoxic neuronal damage. Quinolinic acid (240 nmol in 1 microl) was injected stereotactically into the striatum of male Wistar rats.
F, Block +3 more
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Rolipram inhibition of phosphodiesterase-4 activation
European Journal of Pharmacology: Molecular Pharmacology, 1995Rolipram inhibited U937 cell phosphodiesterase-4 in either the presence or absence of saturating (100 micrograms/ml) phosphatidic acid in an apparently phospholipid-independent manner, exhibiting similar kinetics (Ki values = 0.41 and 0.59 microM, respectively).
M E, DiSanto, R J, Heaslip
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2012 International Conference on Biomedical Engineering and Biotechnology, 2012
In this study we explored that whether PDE inhibitor rolipram affected cholesrterol efflux and ABCA1 expression in THP-1 macrophage foam cells. Cholesterol efflux in THP-1 macrophage-derived foam cells were detected by FJ-2107P type liquid scintillator. The expression of ABCA1 mRNA and protein were determined by RT-PCR and Western blotting respectively.
Ping-Ping He +8 more
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In this study we explored that whether PDE inhibitor rolipram affected cholesrterol efflux and ABCA1 expression in THP-1 macrophage foam cells. Cholesterol efflux in THP-1 macrophage-derived foam cells were detected by FJ-2107P type liquid scintillator. The expression of ABCA1 mRNA and protein were determined by RT-PCR and Western blotting respectively.
Ping-Ping He +8 more
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Lymphocyte Suppression by Rolipram with Other Immunosuppressive Drugs
The Journal of Clinical Pharmacology, 1999Pentoxifylline, a nonselective phosphodiesterase inhibitor, has immunomodulatory activity in vitro and in vivo and potentiates the suppressive effects of glucocorticoids and cyclosporine on lymphocyte proliferation in vitro. Since phosphodiesterase isotypes 3 and 4 predominate in lymphocytes, the authors measured the suppressive effect of rolipram ...
W A, Briggs +5 more
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Pharmacokinetics of the Antidepressant Rolipram in Healthy Volunteers
Xenobiotica, 19891. The pharmacokinetics of rolipram were studied in healthy male volunteers using 3H-rolipram and a radioimmunoassay for measurement of unchanged drug. 2. Rolipram was rapidly and completely absorbed after an oral dose of 1 mg. Bioavailability was 73%. 3. Plasma levels of the unchanged drug declined with a terminal half-life of 2 h. The total clearance
W, Krause, G, Kühne, H, Matthes
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Modulation of corneal endothelial hydration control mechanisms by Rolipram
Pflügers Archiv - European Journal of Physiology, 2000Corneal stromal hydration is maintained by an active HCO3- transport mechanism located in the corneal endothelium. Whilst modulation of transport activity by changes in intracellular cAMP concentration have been noted, the site of effect is undefined. To resolve this question, the effects of Rolipram, a cAMP phosphodiesterase inhibitor, on endothelial ...
C G, Wigham +3 more
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