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Salvia divinorum: all studies

Page 29 of 41: studies 281 to 290 of 407, newest first. Back to the salvia divinorum overview

Research

Pharmacologic hyperreactivity of kappa opioid receptors in periaqueductal gray matter during alcohol withdrawal syndrome in rats.

Pharmacological Reports October 1, 2023 Priscila Vázquez-león, Abraham Miranda-Páez, Hugo Sánchez-Castillo et al.

Periaqueductal gray matter (PAG) is a brain region rich in kappa-opioid receptors (KOR). KOR in PAG mediates behavioral responses related to pain integration, and panic response, among others. Its participation in the addiction phenomena has been poorly studied. Hence, this preliminary study explored the pharmacological effects of KOR stimulation/blockade in dorsal-PAG (D-PAG) during alcohol...

Sex Differences in Kappa Opioid Receptor Agonist Mediated Attenuation of Chemotherapy-Induced Neuropathic Pain in Mice.

Frontiers in Pharmacology 2022 Kelly F Paton, Dan Luo, Anne C. la Flamme et al.

Chemotherapy-induced neuropathic pain is a common side effect for cancer patients which has limited effective treatment options. Kappa opioid receptor (KOR) agonists are a promising alternative to currently available opioid drugs due to their low abuse potential. In the current study, we have investigated the effects of Salvinorin A (SalA) analogues, 16-Ethynyl SalA, 16-Bromo SalA and...

DOI: 10.3389/fphar.2022.813562 (opens in new tab) Full text (opens in new tab) Salvinorin a Chemotherapy-induced neuropathic pain Kappa opioid receptor Paclitaxel +1

Salvindolin elicits opioid system-mediated antinociceptive and antidepressant-like activities.

Journal of Psychopharmacology July 2019 Adam W Keasling, Pankaj Pandey, Robert J Doerksen et al.

Salvinorin A is known as a highly selective kappa opioid receptor agonist with antinociceptive but mostly pro-depressive effects. In this article, we present its new semisynthetic analog with preferential mu opioid affinity, and promising antinociceptive, as well as antidepressant-like activities. Competitive binding studies were performed for salvindolin with kappa opioid and mu opioid. The...

Molecular Signaling Pathways Behind the Biological Effects of Salvia Species Diterpenes in Neuropharmacology and Cardiology.

Phytotherapy Research June 1, 2016 M Akaberi, M Iranshahi, S Mehri

The genus Salvia, from the Lamiaceae family, has diverse biological properties that are primarily attributable to their diterpene contents. There is no comprehensive review on the molecular signaling pathways of these active components. In this review, we investigated the molecular targets of bioactive Salvia diterpenes responsible for the treatment of nervous and cardiovascular diseases. The...

Collybolide is a novel biased agonist of κ-opioid receptors with potent antipruritic activity.

Proceedings of the National Academy of Sciences May 24, 2016 Achla Gupta, Ivone Gomes, Erin N Bobeck et al.

Among the opioid receptors, the κ-opioid receptor (κOR) has been gaining considerable attention as a potential therapeutic target for the treatment of complex CNS disorders including depression, visceral pain, and cocaine addiction. With an interest in discovering novel ligands targeting κOR, we searched natural products for unusual scaffolds and identified collybolide (Colly), a nonnitrogenous...

DOI: 10.1073/pnas.1521825113 (opens in new tab) Full text (opens in new tab) Salvinorin a G-protein–coupled receptors Antinociception Dynorphin +1

Drug models of schizophrenia.

Therapeutic Advances in Psychopharmacology February 1, 2015 Hannah Steeds, Robin Carhart-Harris, James Stone 132 citations

Schizophrenia is a complex mental health disorder with positive, negative and cognitive symptom domains. Approximately one third of patients are resistant to currently available medication. New therapeutic targets and a better understanding of the basic biological processes that drive pathogenesis are needed in order to develop therapies that will improve quality of life for these patients....

Novel Drugs of Abuse: A Snapshot of an Evolving Marketplace.

Adolescent Psychiatry April 1, 2013 Ryan Vandrey, Matthew W Johnson, Patrick S Johnson et al. 26 citations

Over the past decade, non-medical use of novel drugs has proliferated worldwide. In most cases these are synthetic drugs first synthesized in academic or pharmaceutical laboratories for research or drug development purposes, but also include naturally occurring substances that do not fit the typical pharmacological or behavioral profile of traditional illicit substances. Perhaps most unique to...

[Emergent drugs (III): hallucinogenic plants and mushrooms].

Anales del sistema sanitario de Navarra 2013 G Burillo-Putze, E López Briz, B Climent Díaz et al. 14 citations

An increase in the consumption of vegetable substances with a hallucinogenic effect has been observed. Some of these substances are associated with ancestral religious ceremonies, while many of them are legal or are partially regulated. Salvia divinorum is a powerful kappa receptor agonist, with dissociative and hallucinogenic properties, which start quickly and have a short duration. Kratom...

Synthesis of neoclerodane diterpenes and their pharmacological effects.

Topics in current chemistry 2011 Kimberly M Lovell, Katherine M Prevatt-Smith, Anthony Lozama et al. 17 citations

Salvinorin A is a neoclerodane diterpene that has been shown to be an agonist at kappa opioid receptors. Its unique structure makes it an attractive target for synthetic organic chemists due to its seven chiral centers and diterpene scaffold. This molecule is also interesting to pharmacologists because it is a non-serotonergic hallucinogen, and the first opioid ligand discovered that lacks a...

DOI: 10.1007/128_2010_82 (opens in new tab) Full text (opens in new tab) Salvinorin a Chemical synthesis Drug discovery Opioid ligands +1