keyword
https://read.qxmd.com/read/37927136/amelioration-of-morphine-withdrawal-syndrome-by-systemic-and-intranasal-administration-of-mesenchymal-stem-cell-derived-secretome-in-preclinical-models-of-morphine-dependence
#1
JOURNAL ARTICLE
Mauricio Quezada, Carolina Ponce, Pablo Berríos-Cárcamo, Daniela Santapau, Javiera Gallardo, Cristian De Gregorio, María Elena Quintanilla, Paola Morales, Marcelo Ezquer, Mario Herrera-Marschitz, Yedy Israel, Paula Andrés-Herrera, Lucia Hipólito, Fernando Ezquer
BACKGROUND: Morphine is an opiate commonly used in the treatment of moderate to severe pain. However, prolonged administration can lead to physical dependence and strong withdrawal symptoms upon cessation of morphine use. These symptoms can include anxiety, irritability, increased heart rate, and muscle cramps, which strongly promote morphine use relapse. The morphine-induced increases in neuroinflammation, brain oxidative stress, and alteration of glutamate levels in the hippocampus and nucleus accumbens have been associated with morphine dependence and a higher severity of withdrawal symptoms...
November 6, 2023: CNS Neuroscience & Therapeutics
https://read.qxmd.com/read/35936900/mu-opioid-receptor-dependent-transformation-of-respiratory-motor-pattern-in-neonates-in-vitro
#2
JOURNAL ARTICLE
Maia G Gumnit, Jyoti J Watters, Tracy L Baker, Sarah M Johnson, Stephen M Johnson
Endogenous opioid peptides activating mu-opioid receptors (MORs) are part of an intricate neuromodulatory system that coordinates and optimizes respiratory motor output to maintain blood-gas homeostasis. MOR activation is typically associated with respiratory depression but also has excitatory effects on breathing and respiratory neurons. We hypothesized that low level MOR activation induces excitatory effects on the respiratory motor pattern. Thus, low concentrations of an MOR agonist drug (DAMGO, 10-200 nM) were bath-applied to neonatal rat brainstem-spinal cord preparations while recording inspiratory-related motor output on cervical spinal roots (C4-C5)...
2022: Frontiers in Physiology
https://read.qxmd.com/read/34181748/-a-rare-case-of-intravenous-metamizole-abuse
#3
JOURNAL ARTICLE
Şerif Bora Nazlı, Muhammet Sevindik
Given the very frequent prescription of non-opiod analgesics (NOA), their dependence potential has been a subject of research. Increased use of NOA in the last decade has led authors to publish case reports to describe the dependence potential of these agents. Metamizole (dipyrone) has become one of the most popular NOA agents, in being easily accessible and inexpensive. Its analgesic effect depends on the central inhibition of cyclo-oxigenase (COX-3) and activation of the opiodergic and cannabinoid systems...
2021: Türk Psikiyatri Dergisi, Turkish Journal of Psychiatry
https://read.qxmd.com/read/34055568/new-approaches-in-drug-dependence-opioids
#4
REVIEW
Juliane Mielau, Marc Vogel, Stefan Gutwinski, Inge Mick
PURPOSE OF REVIEW: This article aims to provide an overview of standard and adjunctive treatment options in opioid dependence in consideration of therapy-refractory courses. The relevance of oral opioid substitution treatment (OST) and measures of harm reduction as well as heroin-assisted therapies are discussed alongside non-pharmacological approaches. RECENT FINDINGS: Currently, recommendation can be given for OST with methadone, buprenorphine, slow-release oral morphine (SROM), and levomethadone...
May 26, 2021: Current Addiction Reports
https://read.qxmd.com/read/33401948/the-insulin-degrading-enzyme-as-a-link-between-insulin-and-neuropeptides-metabolism
#5
JOURNAL ARTICLE
Dorota Wacławczyk, Jerzy Silberring, Giuseppe Grasso
We have applied a recently developed HPLC-MS enzymatic assay to investigate the cryptic peptides generated by the action of the insulin-degrading enzyme (IDE) on some neuropeptides (NPs) involved in the development of tolerance and dependence to opioids. Particularly, the tested NPs are generated from the NPFF precursor (pro-NPFF (A)): NPFF (FLFQPQRF) and NPAF (AGEGLSSPFWSLAAPQRF). The results show that IDE is able to cleave NPFF and NPAF, generating specific cryptic peptides. As IDE is also responsible for the processing of many other peptides in the brain (amyloid beta protein among the others), we have also performed competitive degradation assays using mixtures of insulin and the above mentioned NPs...
December 2021: Journal of Enzyme Inhibition and Medicinal Chemistry
https://read.qxmd.com/read/32504837/opioid-system-influences-gut-brain-axis-dysbiosis-and-related-alterations
#6
REVIEW
Lola Rueda-Ruzafa, Francisco Cruz, Diana Cardona, Arik J Hone, Guadalupe Molina-Torres, Nuria Sánchez-Labraca, Pablo Roman
Opioid drugs are widely used to treat chronic pain, but their misuse can lead to tolerance, dependence, and addiction and have created a significant public health problem. In addition, food-derived opioid peptides, known as exorphins, like gluten exorphins have been shown to have harmful effects in certain pathologies like celiac disease, for example. Several studies support the involvement of the opioid system in the development of disorders such as autism spectrum syndrome. Moreover, bidirectional communication between the intestine and brain has been shown to be altered in various neurodegenerative diseases including Alzheimer´s and Parkinson´s...
September 2020: Pharmacological Research: the Official Journal of the Italian Pharmacological Society
https://read.qxmd.com/read/32072918/potential-mechanisms-involved-in-the-anticonvulsant-effect-of-methanol-extract-of-pyrenancantha-staudtii-in-mice
#7
JOURNAL ARTICLE
Olayemi K Wakeel, Oluropo B Awosan, Oyetunji T Kolawole, Akeem A Ayankunle, Olukunle J Onaolapo, Oluwaseyi A Adeyeba
OBJECTIVE: To determine the potential effect of Pyrenancantha staudtii extract on experimentally induced seizures in mice and to evaluate the role of benzodiazepines, naloxone, and serotonin within these pathways. METHODS: Animal behaviours were evaluated using open field, hexobarbitone-induced sleep model, and anticonvulsant activity using picrotoxin-, or strychnine-, or isoniazid-induced convulsions. Attempt to understand the mode of action of the anticonvulsant activity of the plant, three notable antagonists (flumazenil, 3 mg/kg; naloxone 5 mg/kg, i...
2020: Central Nervous System Agents in Medicinal Chemistry
https://read.qxmd.com/read/29653244/opioid-use-following-cervical-spine-surgery-trends-and-factors-associated-with-long-term-use
#8
JOURNAL ARTICLE
Andrew J Pugely, Nicholas A Bedard, Piyush Kalakoti, Nathan R Hendrickson, Jamal N Shillingford, Joseph L Laratta, Comron Saifi, Ronald A Lehman, K Daniel Riew
BACKGROUND CONTEXT: Limited or no data exist evaluating risk factors associated with prolonged opioid use following cervical arthrodesis. PURPOSE: The objectives of this study were to assess trends in postoperative narcotic use among preoperative opioid users (OUs) versus non-opioid users (NOUs) and to identify factors associated with postoperative narcotic use at 1 year following cervical arthrodesis. STUDY DESIGN/SETTING: This is a retrospective observational study...
November 2018: Spine Journal: Official Journal of the North American Spine Society
https://read.qxmd.com/read/29248440/jtc801-induces-ph-dependent-death-specifically-in-cancer-cells-and-slows-growth-of-tumors-in-mice
#9
JOURNAL ARTICLE
Xinxin Song, Shan Zhu, Yangchun Xie, Jiao Liu, Lingyi Sun, Dexing Zeng, Pengcheng Wang, Xiaochao Ma, Guido Kroemer, David L Bartlett, Timothy R Billiar, Michael T Lotze, Herbert J Zeh, Rui Kang, Daolin Tang
BACKGROUND & AIMS: Maintenance of acid-base homeostasis is required for normal physiology, metabolism, and development. It is not clear how cell death is activated in response to changes in pH. We performed a screen to identify agents that induce cell death in a pH-dependent manner (we call this alkaliptosis) in pancreatic ductal adenocarcinoma cancer (PDAC) cells and tested their effects in mice. METHODS: We screened a library of 254 compounds that interact with G-protein-coupled receptors (GPCRs) to identify those with cytotoxic activity against a human PDAC cell line (PANC1)...
April 2018: Gastroenterology
https://read.qxmd.com/read/26922659/antagonist-models-for-relapse-prevention-and-reducing-hiv-risk
#10
REVIEW
George E Woody, Evgeny Krupitsky, Edwin Zvartau
Naltrexone is an antagonist that binds tightly to μ-opioid receptors and blocks the subjective and analgesic effects of opioids. It does not produce physiologic dependence and precipitates withdrawal if administered to an opioid dependent person, thus starting it must begin with detoxification. It was first available in the mid-1970s as a 50 mg tablet that blocked opioids for 24-36 h if taken daily, or every 2-3 days at higher doses - for example: 100 mg Monday and Wednesday, 150 mg on Friday...
September 2016: Journal of Neuroimmune Pharmacology: the Official Journal of the Society on NeuroImmune Pharmacology
https://read.qxmd.com/read/25942373/antinociceptive-activity-and-toxicity-evaluation-of-the-fatty-oil-from-plukenetia-polyadenia-mull-arg-euphorbiaceae
#11
JOURNAL ARTICLE
Amanda S Mota, Anderson B de Lima, Thayana Lucy F Albuquerque, Tiago S Silveira, José Luiz M do Nascimento, Joyce Kelly R da Silva, Alcy F Ribeiro, José Guilherme S Maia, Gilmara N T Bastos
Seed oil (Pp-oil) of Plukenetia polyadenia is used by native people of the Brazilian Amazon against arthritis and rheumatism, spreading it on the arms and legs to reduce the pain and inflammation. Pp-oil was obtained by pressing dried seeds at room temperature to give a 47.0% yield of oil. It was then subjected to fatty acid composition analysis. The principal fatty acids were linoleic acid (46.5%), α-linolenic acid (34.4%) and oleic acid (13.9%). Then, it was evaluated for its antinociceptive activity in mice, using the acetic acid-induced abdominal writhing, hot plate and formalin test models...
April 30, 2015: Molecules: a Journal of Synthetic Chemistry and Natural Product Chemistry
https://read.qxmd.com/read/23050896/tramadol-versus-clonidine-in-management-of-heroin-withdrawl
#12
JOURNAL ARTICLE
Somsubhra Chattopadhyay, O P Singh, Amit Bhattacharyya, Subrata Sen, Paromita Roy, Sharmistha Debnath
UNLABELLED: Opiod dependence is one of the leading psychiatric morbidities in India. The deaddiction centres are meager in number; stigma attached to admission in deaddiction centre is high and most addicts want outpatient treatment so that they do not miss daily wages. Several recent reports stated effectiveness of tramadol in treating opioid withdrawal. This study attempts to compare effectiveness of tramadol with clonidine in opioid withdrawal. METHODOLOGY: A total of 60 patients having heroin dependence were selected and out of them 30 got clonidine treatment and the other 30 got tramadol treatment...
December 2010: Asian Journal of Psychiatry
https://read.qxmd.com/read/22828157/budgetary-impact-analysis-of-buprenorphine-naloxone-combination-suboxone%C3%A2-in-spain
#13
JOURNAL ARTICLE
Jose Martinez-Raga, Francisco Gonzalez-Saiz, Julian Oñate, Itziar Oyagüez, Eliazar Sabater, Miguel A Casado
BACKGROUND: Opioid addiction is a worldwide problem. Agonist opioid treatment (AOT) is the most widespread and frequent pharmacotherapeutic approach. Methadone has been the most widely used AOT, but buprenorphine, a partial μ-opiod agonist and a κ-opiod antagonist, is fast gaining acceptance. The objective was to assess the budgetary impact in Spain of the introduction of buprenorphine-naloxone (B/N) combination. METHODS: A budgetary impact model was developed to estimate healthcare costs of the addition of B/N combination to the therapeutic arsenal for treating opioid dependent patients, during a 3-year period under the National Health System perspective...
March 29, 2012: Health Economics Review
https://read.qxmd.com/read/22581981/outcomes-in-a-sample-of-opiod-dependent-clients-treated-under-california-s-proposition-36
#14
JOURNAL ARTICLE
Jongserl Chun, Joseph R Guydish, James L Sorensen, Nancy A Haug, Siara Andrews, Larry Nelson
This study evaluated treatment outcomes for the reduction of criminal justice involvement and substance use among opioid dependent clients in a therapeutic community setting under California's Proposition 36. We compared treatment outcomes between those mandated to treatment under Proposition 36 (n = 24) and those on probation but not involved in Proposition 36 (n = 61) over 12 months. Over time, both groups showed significant improvement on drug use and employment measures, were more likely to be involved in job training and less likely to be engaged in work activity, and had similar retention in treatment...
July 1, 2007: Journal of Drug Issues
https://read.qxmd.com/read/22530273/-buprenorphin-and-benzodiazepines-an-association-with-high-risk-reality-of-co-prescriptions-by-the-general-practitioners
#15
JOURNAL ARTICLE
Paolo Di Patrizio, Sophie Houille, Raymund Schwan, Jean-Marc Boivin
BACKGROUND: The buprenorphine (BHD) is an effective maintenance treatment for opioid dependence, used in France until 1996. From 1996 to 2001, it is involved in 137 deaths by respiratory depression including 91 attributable to the benzodiazepines (BDZ) association. The number of deaths caused by the BHD and BDZ, when they are taken jointly, is probably underestimated. The reasons for this association are the misuse, the self-medication and the co-prescription. OBJECTIVE: The objective of this study was to assess the co-prescription of these two drugs by the general practitioners (GPs) of Nancy (France)...
December 20, 2010: La Revue du Praticien
https://read.qxmd.com/read/22459341/a-randomized-placebo-controlled-study-of-pregabalin-for-postoperative-pain-intensity-after-laparoscopic-cholecystectomy
#16
RANDOMIZED CONTROLLED TRIAL
Fatih Balaban, Seyhan Yağar, Ayşegül Özgök, Mihrican Koç, Hayriye Güllapoğlu
STUDY OBJECTIVE: To determine the efficacy of two different doses (150 mg and 300 mg) of preoperative pregabalin on pain relief and total opioid consumption after laparoscopic cholecystectomy. DESIGN: Prospective, randomized, placebo-controlled, double-blinded study. SETTING: Training and research hospital. PATIENTS: 90 adult, ASA physical status 1 and 2 patients. INTERVENTIONS: Patients were randomly assigned to three groups to receive orally one hour before surgery, a placebo (Group 1), pregabalin 150 mg (Group 2), or pregabalin 300 mg (Group 3)...
May 2012: Journal of Clinical Anesthesia
https://read.qxmd.com/read/20522981/antinociceptive-effects-of-docosahexaenoic-acid-against-various-pain-stimuli-in-mice
#17
JOURNAL ARTICLE
Kazuo Nakamoto, Takashi Nishinaka, Mitsumasa Mankura, Wakako Fujita-Hamabe, Shogo Tokuyama
Docosahexaenoic acid (DHA), an omega-3 polyunsaturated fatty acid (n-3 PUFAs), is an essential polyunsaturated fatty acid in the central nervous system, and possesses many physiological functions in neurodegenerative diseases. Previously, there are some reports that n-3 PUFAs contribute to pain relief. As the antinociceptive effect of DHA alone has not been reported, this study examined the antinociceptive effect of DHA on various pain stimuli. To evaluate the antinociceptive effect of DHA on thermal and chemical nociception, we employed the tail flick test, acetic acid writhing test and formalin test in mice...
2010: Biological & Pharmaceutical Bulletin
https://read.qxmd.com/read/20455185/-drug-addiction-and-anaesthesia-most-popular-recreational-drugs-in-germany-and-anaesthesiological-management-of-drug-addicts
#18
JOURNAL ARTICLE
Ingrid Rundshagen
Drug addicts need special anesthesiological care due to their co-morbidities, their modified need for analgesics and anesthetics and/or their specific substitution therapies. In spite of the high incidence of addiction worldwide controlled studies and evidence based recommendations for the anaesthesiological management of the patients are missing. The perioperative care is not the treatment of addiction, on the contrary the specific aspects of a chronic disease have to be accepted. Equally important perioperative treatment strategies for the management of drug addicts include: 1...
May 2010: Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie: AINS
https://read.qxmd.com/read/19570226/genetic-variation-in-the-serotonin-transporter-gene-5-httlpr-rs25531-influences-the-analgesic-response-to-the-short-acting-opioid-remifentanil-in-humans
#19
JOURNAL ARTICLE
Eva Kosek, Karin B Jensen, Tina B Lonsdorf, Martin Schalling, Martin Ingvar
BACKGROUND: There is evidence from animal studies that serotonin (5-HT) can influence the antinociceptive effects of opioids at the spinal cord level. Therefore, there could be an influence of genetic polymorphisms in the serotonin system on individual variability in response to opioid treatment of pain. The serotonin transporter (5-HTT) is a key regulator of serotonin metabolism and availability and its gene harbors several known polymorphisms that are known to affect 5-HTT expression (e...
July 1, 2009: Molecular Pain
https://read.qxmd.com/read/18433502/association-between-single-nucleotide-polymorphisms-in-the-mu-opioid-receptor-gene-oprm1-and-self-reported-responses-to-alcohol-in-american-indians
#20
JOURNAL ARTICLE
Cindy L Ehlers, Penelope A Lind, Kirk C Wilhelmsen
BACKGROUND: Variation in response to the hedonic and adverse effects of a substance is in part an inherited factor that may influence its use, abuse and dependence. The mu opioid receptor is the primary site of action for opiates and individuals with polymorphisms in this receptor appear to have variation in the CNS effects of opiates. Several studies have suggested that this receptor may also mediate some of the effects of non-opioid drugs, such as alcohol. The purpose of this study was to investigate associations between 13 single nucleotide polymorphisms in the mu opioid receptor gene (OPRM1) with self-reported responses to alcohol, an endophenotype associated with the development of alcohol dependence, in American Indians living on eight contiguous reservations...
April 23, 2008: BMC Medical Genetics
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