User profiles for F. Sakloth
Farhana SaklothDepartment of Neuroscience.Icahn School of Medicine at Mount Sinai Verified email at mssm.edu Cited by 610 |
Structural modification of the designer stimulant α-pyrrolidinovalerophenone (α-PVP) influences potency at dopamine transporters
α-Pyrrolidinovalerophenone (α-PVP, 7) is an illegal synthetic stimulant that is being sold on
the clandestine market as “flakka” and “gravel”. The potent pharmacological effects of α-PVP …
the clandestine market as “flakka” and “gravel”. The potent pharmacological effects of α-PVP …
Regulators of G protein signaling in analgesia and addiction
F Sakloth, C Polizu, F Bertherat, V Zachariou - Molecular Pharmacology, 2020 - ASPET
Regulator of G protein signaling (RGS) proteins are multifunctional proteins expressed in
peripheral and neuronal cells, playing critical roles in development, physiologic processes, …
peripheral and neuronal cells, playing critical roles in development, physiologic processes, …
Oxycodone withdrawal induces HDAC1/HDAC2-dependent transcriptional maladaptations in the reward pathway in a mouse model of peripheral nerve injury
… unpaired two-tailed t-tests after an F test for variance. Results for behavioral and biochemical
studies are expressed as the mean ± sem F and t values for each dataset and analysis are …
studies are expressed as the mean ± sem F and t values for each dataset and analysis are …
“Deconstruction” of the abused synthetic cathinone methylenedioxypyrovalerone (MDPV) and an examination of effects at the human dopamine transporter
R Kolanos, E Solis Jr, F Sakloth… - ACS chemical …, 2013 - ACS Publications
Synthetic cathinones, β-keto analogues of amphetamine (or, more correctly, of phenylalkylamines),
represent a new and growing class of abused substances. Several such analogues …
represent a new and growing class of abused substances. Several such analogues …
Quantitative structure–activity relationship analysis of the pharmacology of para‐substituted methcathinone analogues
Background and Purpose Methcathinone ( MCAT ) is a potent monoamine releaser and parent
compound to emerging drugs of abuse including mephedrone (4‐ CH 3 MCAT ), the para…
compound to emerging drugs of abuse including mephedrone (4‐ CH 3 MCAT ), the para…
Abuse-related neurochemical effects of para-substituted methcathinone analogs in rats: microdialysis studies of nucleus accumbens dopamine and serotonin
JA Suyama, F Sakloth, R Kolanos, RA Glennon… - … of Pharmacology and …, 2016 - ASPET
Methcathinone (MCAT) is a monoamine releaser and parent compound to a new class of
designer drugs that includes the synthetic cathinones mephedrone and flephedrone. Using …
designer drugs that includes the synthetic cathinones mephedrone and flephedrone. Using …
Effects of acute and repeated treatment with serotonin 5-HT2A receptor agonist hallucinogens on intracranial self-stimulation in rats.
F Sakloth, E Leggett, MJ Moerke… - Experimental and …, 2019 - psycnet.apa.org
… The right panels (B, D, and F) show the number of stimulations per component collapsed
across all frequencies. Abscissae: Drug dose in mg kg-1. Ordinates: Percentage of baseline …
across all frequencies. Abscissae: Drug dose in mg kg-1. Ordinates: Percentage of baseline …
Steric parameters, molecular modeling and hydropathic interaction analysis of the pharmacology of para‐substituted methcathinone analogues
Background and Purpose There is growing concern over the abuse of certain psychostimulant
methcathinone ( MCAT ) analogues. This study extends an initial quantitative structure–…
methcathinone ( MCAT ) analogues. This study extends an initial quantitative structure–…
[HTML][HTML] A promising chemical series of positive allosteric modulators of the μ-opioid receptor that enhance the antinociceptive efficacy of opioids but not their adverse …
Positive allosteric modulators (PAMs) of the μ-opioid receptor (MOR) have been proposed to
exhibit therapeutic potential by maximizing the analgesic properties of clinically used opioid …
exhibit therapeutic potential by maximizing the analgesic properties of clinically used opioid …
HDAC6-selective inhibitors decrease nerve-injury and inflammation-associated mechanical hypersensitivity in mice
F Sakloth, L Manouras, K Avrampou, V Mitsi… - …, 2020 - Springer
Background HDAC6 is a class IIB histone deacetylase expressed at many levels of the
nociceptive pathway. This study tested the ability of novel and selective HDAC6 inhibitors to …
nociceptive pathway. This study tested the ability of novel and selective HDAC6 inhibitors to …