Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Kethireddy V.V. Ananthalakshmi"'
Publikováno v:
Developmental & Comparative Immunology. 74:200-208
We recently demonstrated Ang 1–7 reduced inflammation in the dextran sulfate sodium (DSS) colitis model. In this study we examined the effect of Ang 1–7 on modulation of plasma levels of selected cytokines and chemokines and immune cell effector
Autor:
Mohamed G. Qaddoumi, Kethireddy V.V. Ananthalakshmi, Ivan O. Edafiogho, Oludotun A. Phillips, Samuel B. Kombian
Publikováno v:
European Journal of Medicinal Chemistry. 76:20-30
Due to the excellent anticonvulsant activity of previously synthesized halogenated enaminones, more disubstituted analogs were synthesized and evaluated in vitro. The new enaminones either had no effect, depressed, or enhanced population spike (PS) a
Anti-Inflammatory Properties of the Enaminone E121 in the Dextran Sulfate Sodium (DSS) Colitis Model
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 12, p e0168567 (2016)
PLoS ONE, Vol 11, Iss 12, p e0168567 (2016)
Background Enaminones are synthetic compounds with an established role in the prevention of various forms of seizures. Recent evidence suggests potent anti-tussive, bronchodilation and anti-inflammatory properties. Pre-treatment with particularly E12
Publikováno v:
Medical Principles and Practice. 17:365-372
Objectives: We tested if E139, an anticonvulsant enaminone, interacts with norepinephrine (NE) to suppress population responses and chemically induced in vitro seizures in the rat hippocampus. Materials and Methods: Evoked field population spikes (PS
Autor:
Noha N. Salama, Natalie D. Eddington, Ivan O. Edafiogho, Kethireddy V.V. Ananthalakshmi, Samuel B. Kombian, Patrice L. Jackson, K. R. Scott, Mariano S. Alexander, Tiffany L. Wilson, Clive D. Hanson
Publikováno v:
Journal of Pharmaceutical Sciences. 96:2509-2531
Enaminones, enamines of beta-dicarbonyl compounds, have been known for many years. Their early use has been relegated to serving as synthetic intermediates in organic synthesis and of late, in pharmaceutical development. Recently, the therapeutic pot
Publikováno v:
Epilepsy Research. 76:85-92
Some enaminones are reported to have in vivo anticonvulsant activity. We asked if methyl 4-(4'-bromophenyl)aminocyclohex-3-en-6-methyl-2-oxo-1-oate (E139), one of such enaminones produced in vitro effects that may underlie or explain these in vivo an
Autor:
Subramanian S. Parvathy, Samuel B. Kombian, Kethireddy V.V. Ananthalakshmi, Wandikayi C. Matowe
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 84:203-211
We recently reported that the activation of cholecystokinin-2 receptors depress evoked excitatory postsynaptic currents (EPSCs) in nucleus accumbens (NAc) indirectly through γ-aminobutyric acid (GABA) acting on γ-aminobutyric acid-B (GABAB) recepto
Publikováno v:
Neuroscience. 141:345-356
Enaminones are a novel group of compounds some of which possess anticonvulsant activity in in vivo animal models of seizures. We recently reported that some enaminones, including methyl 4-(4'-bromophenyl)aminocyclohex-3-en-6-methyl-2-oxo-1-oate, depr
Publikováno v:
British Journal of Pharmacology. 145:945-953
Enaminones are a novel group of compounds that have been shown to possess anticonvulsant activity in in vivo animal models of seizures. The cellular mechanism by which these compounds produce their anticonvulsant effects is not yet known. This study
Autor:
Kethireddy V.V. Ananthalakshmi, Subramanian S. Parvathy, Samuel B. Kombian, Wandikayi C. Matowe
Publikováno v:
Journal of Neuroscience Research. 79:412-420
We recently reported that cholecystokinin (CCK) excited nucleus accumbens (NAc) cells and depressed excitatory synaptic transmission indirectly through gamma-aminobutyric acid (GABA), acting on presynaptic GABAB receptors (Kombian et al. [2004] J. Ph