keyword
https://read.qxmd.com/read/24277251/effect-of-thyrotropin-releasing-hormone-on-lipoxygenase-induced-hypotension-in-the-unanesthetized-guinea-pig
#21
JOURNAL ARTICLE
W E Lux, G Feuerstein, A I Faden
Soybean lipoxygenase, an enzyme which catalyzes the formation of the vasoactive lipid 15-hydroperoxy eicosatetraenoic acid (15-HPETE) from arachidonic acid, was administered to unanesthetized guinea pigs previously prepared with indwelling vascular cannulae for continuous cardiovascular monitoring. Administration of this enzyme (150 mg/kg IV) resulted in profound hypotension in this model, but no cardiovascular change was observed after administration of equal weight or equimolar amounts of another protein (ovalbumin)...
May 1984: Pharmaceutical Research
https://read.qxmd.com/read/23699079/cocaine-washout-syndrome-a-rare-case-presentation-with-refractory-shock
#22
Ji Hyun Rhee, V Sandeep Yadavalli, Parit Mekaroonkamol, Rene Franco, K Randall Young, Adam Rowden
SESSION TYPE: Critical Care Student/Resident Case Report Posters IIPRESENTED ON: Tuesday, October 23, 2012 at 01:30 PM - 02:30 PMINTRODUCTION: Cocaine washout syndrome (CWS) is a rare complication caused by prolonged cocaine use, manifested by brief coma that resolves spontaneously. The proposed mechanism is depletion of adrenergic neurotransmitters due to prolonged and persistent stimulation. There are only 3 cases reported in the literature and the incidence of this syndrome is unknown. Here, we report an unusually extreme case of CWS presenting with coma and refractory shock...
October 1, 2012: Chest
https://read.qxmd.com/read/23603410/accumbal-opioid-receptors-modulate-cue-competition-in-one-trial-overshadowing
#23
JOURNAL ARTICLE
Mihaela D Iordanova, Tatiana Haralambous, Gavan P McNally, R Frederick Westbrook
The contribution of opioid receptors in the nucleus accumbens to contextual and auditory fear conditioning was examined. Impairment in contextual fear conditioning was found when training occurred under accumbal infusions of the opioid receptor agonist morphine in a dose-dependent and receptor specific fashion, only when shock onset coincided with auditory stimulus offset. Contextual fear conditioning was spared, however when the delivery of shock was not signalled by an auditory stimulus, the auditory stimulus was of low intensity (70dB), or an interval (10s or 30s) was interpolated between auditory stimulus offset and shock onset...
June 23, 2013: Brain Research
https://read.qxmd.com/read/23431888/-naloxone
#24
JOURNAL ARTICLE
Daisuke Setoguchi, Yasuyuki Kakihana
Naloxone hydrochloride is an agent capable of antagonizing respiratory depression and analgesic actions which are inherent to the opioid by competitively acting at opioid receptors. It greatly contributed to basic research on antagonistic action of opioid receptors due to its high affinity to opioid receptors, in particular, micro-receptor. Naloxone has been recommended as an analeptic agent at a guideline level for patients with revealed or suspicious opioid addiction. Further, it has also been used as a preventive and treatment agent for spinal cord ischemia...
January 2013: Masui. the Japanese Journal of Anesthesiology
https://read.qxmd.com/read/23244733/interaction-of-the-synthetic-peptide-octarphin-with-rat-adrenal-cortex-membranes
#25
JOURNAL ARTICLE
Y N Nekrasova, Y A Zolotarev, E V Navolotskaya
The synthetic peptide octarphin (TPLVTLFK, fragment 12-19 of β-endorphin), a selective agonist of the non-opioid β-endorphin receptor, was labeled with tritium yielding specific activity of 28 Ci/mmol. The binding of [3H]octarphin to rat adrenal cortex membranes was studied under normal conditions as well as after cold and heat shocks. It was found that under normal conditions [(3)H]octarphin specifically binds to the membranes with high affinity: K(d1) = 36.3 ± 2.5 nM, B(max1) = 41.0 ± 3.8 pmol/mg protein...
December 2012: Biochemistry. Biokhimii︠a︡
https://read.qxmd.com/read/22647273/morphine-withdrawal-activates-hypothalamic-pituitary-adrenal-axis-and-heat-shock-protein-27-in-the-left-ventricle-the-role-of-extracellular-signal-regulated-kinase
#26
JOURNAL ARTICLE
E Martínez-Laorden, M A Hurle, M V Milanés, M L Laorden, P Almela
The negative affective states of withdrawal involve the recruitment of brain and peripheral stress circuitry [e.g., noradrenergic activity, induction of the hypothalamo-pituitary-adrenocortical (HPA) axis, and the expression and activation of heat shock proteins (Hsps)]. The present study investigated the role of extracellular signal-regulated protein kinase (ERK) and β-adrenoceptor on the response of stress systems to morphine withdrawal by the administration of [amino[(4-aminophenyl)thio]methylene]-2-(trifluoromethyl)benzeneacetonitrile (SL327), a selective inhibitor of ERK activation, or propranolol (a β-adrenoceptor antagonist)...
September 2012: Journal of Pharmacology and Experimental Therapeutics
https://read.qxmd.com/read/22285390/geranylgeranylacetone-protects-mice-against-morphine-induced-hyperlocomotion-rewarding-effect-and-withdrawal-syndrome
#27
JOURNAL ARTICLE
Fu-Cheng Luo, Lei Qi, Tao Lv, Sheng-Dong Wang, Hua Liu, Hajime Nakamura, Junji Yodoi, Jie Bai
There are few efficacious interventions to combat morphine dependence. Thioredoxin-1 (Trx-1) and heat shock protein 70 (Hsp70) are emerging as important modulators of neuronal function. They have been shown to be involved in cellular protective mechanisms against a variety of toxic stressors. This study was designed to investigate the effects of geranylgeranylacetone (GGA), a pharmacological inducer of Trx-1 and Hsp70, on morphine-induced hyperlocomotion, rewarding effect, and withdrawal syndrome. Trx-1 and Hsp70 expression was increased in the frontal cortex, hippocampus, ventral tegmental area, and nucleus accumbens of mice after GGA treatment...
April 1, 2012: Free Radical Biology & Medicine
https://read.qxmd.com/read/22229842/the-dose-response-relation-for-the-antinociceptive-effect-of-morphine-in-a-fish-rainbow-trout
#28
JOURNAL ARTICLE
S G Jones, C Kamunde, K Lemke, E D Stevens
There have been suggestions that analgesics be used by fish researchers. But in the absence of dose-response data for morphine, this suggestion seems imprudent. The purpose of the present study was to develop a dose-response relationship in fish using six doses of morphine. The response (movement of the fins or tail) to a noxious stimulus (electrical shock to the face region) was monitored before and after a dose of morphine intraperitoneally (i.p.). The i.p. dose of morphine ED(50) in rainbow trout was 6.7 ± 0...
December 2012: Journal of Veterinary Pharmacology and Therapeutics
https://read.qxmd.com/read/22043286/chronic-morphine-alters-the-presynaptic-protein-profile-identification-of-novel-molecular-targets-using-proteomics-and-network-analysis
#29
JOURNAL ARTICLE
Noura S Abul-Husn, Suresh P Annangudi, Avi Ma'ayan, Dinah L Ramos-Ortolaza, Steven D Stockton, Ivone Gomes, Jonathan V Sweedler, Lakshmi A Devi
Opiates produce significant and persistent changes in synaptic transmission; knowledge of the proteins involved in these changes may help to understand the molecular mechanisms underlying opiate dependence. Using an integrated quantitative proteomics and systems biology approach, we explored changes in the presynaptic protein profile following a paradigm of chronic morphine administration that leads to the development of dependence. For this, we isolated presynaptic fractions from the striata of rats treated with saline or escalating doses of morphine, and analyzed the proteins in these fractions using differential isotopic labeling...
2011: PloS One
https://read.qxmd.com/read/21586652/morphine-induced-cardiogenic-shock
#30
JOURNAL ARTICLE
Colin Feeney, Chizobam Ani, Naini Sharma, Tom Frohlich
OBJECTIVE: Although animal and human models suggest that direct suppression of myocardial contractility may occur with morphine administration, to our knowledge, clinical observation of this potentially important effect has not been reported. This case report presents a unique case of morphine-induced transient reversible cardiogenic shock. CASE SUMMARY: A 44-year-old woman with a history of hypertension, diabetes, and asthma presented with a 3-day history of epigastric pain...
June 2011: Annals of Pharmacotherapy
https://read.qxmd.com/read/21530534/naloxone-precipitated-morphine-withdrawal-evokes-phosphorylation-of-heat-shock-protein-27-in-rat-heart-through-extracellular-signal-regulated-kinase
#31
JOURNAL ARTICLE
P Almela, E Martínez-Laorden, N M Atucha, M V Milanés, M L Laorden
Heat shock protein 27 (Hsp27) is a well-known stress response protein that becomes phosphorylated through extracellular signal-regulated kinase (ERK). Different drugs of abuse, such as morphine and/or its withdrawal, induce severe stress situations. In this study, we investigated Hsp27 and phospho-Hsp27 expression during morphine dependence and withdrawal and evaluated the involvement of ERK in the phosphorylation of Hsp27 in the rat right ventricle. Dependence on morphine was induced by a 7-day s.c. implantation of morphine pellets...
July 2011: Journal of Molecular and Cellular Cardiology
https://read.qxmd.com/read/21107581/involvement-of-the-opioid-system-in-the-hypokinetic-state-induced-in-cockroaches-by-a-parasitoid-wasp
#32
JOURNAL ARTICLE
Tali Gavra, Frederic Libersat
The parasitoid wasp Ampulex compressa stings and injects venom into the cockroach brain to induce a long-lasting hypokinetic state. This state is characterized by decreased responsiveness to aversive stimuli, suggesting the manipulation of a neuromodulatory system in the cockroach's central nervous system. A likely candidate is the opioid system, which is known to affect responsiveness to stimuli in insects. To explore this possibility, we injected cockroaches with different opioid receptor agonists or antagonists before they were stung by a wasp and tested the escape behavior of these cockroaches to electric foot shocks...
March 2011: Journal of Comparative Physiology. A, Neuroethology, Sensory, Neural, and Behavioral Physiology
https://read.qxmd.com/read/20888871/influence-of-three-day-morphine-treatment-upon-impairment-of-memory-consolidation-induced-by-cannabinoid-infused-into-the-dorsal-hippocampus-in-rats
#33
JOURNAL ARTICLE
Mohammad Reza Zarrindast, Majid Navaeian, Mohammad Nasehi
In the present study, the effects of morphine treatment upon reduction of memory consolidation by post-training administration of the non-selective cannabinoid CB(1)/CB(2) receptor agonist, WIN55,212-2, into the dorsal hippocampus (intra-CA1) have been investigated in rats. Step-through inhibitory avoidance apparatus was used to test memory retrieval, which was made of two white and dark compartments. In training day, electric shocks were delivered to the grid floor of the dark compartment. On the test day, the animal was placed in the white compartment and allowed to enter the dark compartment...
January 2011: Neuroscience Research
https://read.qxmd.com/read/20642252/outcome-of-acute-heroin-overdose-requiring-intensive-care-unit-admission
#34
JOURNAL ARTICLE
Leonidas Grigorakos, Katerina Sakagianni, Evdoxia Tsigou, George Apostolakos, Giannis Nikolopoulos, Dimitris Veldekis
BACKGROUND: Heroin use carries a large burden of morbidity and mortality. Heroin overdose and in particular events that need intensive care unit (ICU) admission have not been widely examined. The aim of this study was to describe the causes of ICU admission and the outcome of patients with a heroin overdose. METHODS: A retrospective chart review of all patients with a heroin overdose admitted to the ICU between 1987 and 2006 was conducted. RESULTS: Forty-two records were available for review...
May 2010: Journal of Opioid Management
https://read.qxmd.com/read/20098709/endogenous-morphine-levels-are-increased-in-sepsis-a-partial-implication-of-neutrophils
#35
JOURNAL ARTICLE
Elise Glattard, Ingeborg D Welters, Thomas Lavaux, Arnaud H Muller, Alexis Laux, Dan Zhang, Alexander R Schmidt, François Delalande, Benoît-Joseph Laventie, Sylvie Dirrig-Grosch, Didier A Colin, Alain Van Dorsselaer, Dominique Aunis, Marie-Hélène Metz-Boutigue, Francis Schneider, Yannick Goumon
BACKGROUND: Mammalian cells synthesize morphine and the respective biosynthetic pathway has been elucidated. Human neutrophils release this alkaloid into the media after exposure to morphine precursors. However, the exact role of endogenous morphine in inflammatory processes remains unclear. We postulate that morphine is released during infection and can be determined in the serum of patients with severe infection such as sepsis. METHODOLOGY: The presence and subcellular immunolocalization of endogenous morphine was investigated by ELISA, mass spectrometry analysis and laser confocal microscopy...
2010: PloS One
https://read.qxmd.com/read/19833175/evidence-that-intrathecal-morphine-3-glucuronide-may-cause-pain-enhancement-via-toll-like-receptor-4-md-2-and-interleukin-1beta
#36
JOURNAL ARTICLE
S S Lewis, M R Hutchinson, N Rezvani, L C Loram, Y Zhang, S F Maier, K C Rice, L R Watkins
Morphine-3-glucoronide (M3G) is a major morphine metabolite detected in cerebrospinal fluid of humans receiving systemic morphine. M3G has little-to-no affinity for opioid receptors and induces pain by unknown mechanisms. The pain-enhancing effects of M3G have been proposed to significantly and progressively oppose morphine analgesia as metabolism ensues. We have recently documented that morphine activates toll-like receptor 4 (TLR4), beyond its classical actions on mu-opioid receptors. This suggests that M3G may similarly activate TLR4...
January 20, 2010: Neuroscience
https://read.qxmd.com/read/19572940/phosphodiesterase-inhibition-by-naloxone-augments-the-inotropic-actions-of-beta-adrenergic-stimulation
#37
JOURNAL ARTICLE
W K Park, C H Chang, J E Chae, M H Kim, Y L Cho, D S Ahn
BACKGROUND: In a shock state, naloxone generates the cardiovascular pressor effect by displacing the endogenous opiate-like peptide beta-endorphin, resulting in restoration of the normal response to catecholamines. In addition to this opioid antagonistic effect, the non-opiate receptor-mediated effect has also been proposed. The aim of this study was to define the mechanism of non-opiate receptor-mediated action of naloxone. METHODS: In guinea-pig ventricular tissues, cumulative concentration-response curves for isoproterenol as well as for forskolin and 3-isobutylmethylxanthine (IBMX) were obtained by increasing the concentration stepwise...
September 2009: Acta Anaesthesiologica Scandinavica
https://read.qxmd.com/read/18854195/role-of-cholinergic-opioidergic-and-gabaergic-neurotransmission-of-the-dorsal-hippocampus-in-the-modulation-of-nociception-in-guinea-pigs
#38
JOURNAL ARTICLE
Lys Angela Favaroni Mendes, Leda Menescal-de-Oliveira
AIMS: Several physiological, pharmacological and behavioral lines of evidence suggest that the hippocampal formation is involved in nociception. The hippocampus is also believed to play an important role in the affective and motivational components of pain perception. Thus, our aim was to investigate the participation of cholinergic, opioidergic and GABAergic systems of the dorsal hippocampus (DH) in the modulation of nociception in guinea pigs. MAIN METHODS: The test used consisted of the application of a peripheral noxious stimulus (electric shock) that provokes the emission of a vocalization response by the animal...
November 7, 2008: Life Sciences
https://read.qxmd.com/read/18849879/chronic-morphine-application-is-protective-against-cell-death-in-primary-human-neurons
#39
JOURNAL ARTICLE
Jia Cui, Qiuyue Chen, Long-Chuan Yu, Yan Zhang
Morphine addiction has become a long-time, serious medical and social problem. To understand the cellular mechanisms of morphine application and addiction, the effects of chronic morphine treatments were examined in primary cultured human neurons. Our results show that, surprisingly, morphine protects cultured human neurons against serum deprivation and staurosporine induced cytotoxicity. Morphine downregulates proapoptotic factor Bax levels in cultured human neurons. In addition, heat shock protein 70 is also involved in morphine protection...
December 3, 2008: Neuroreport
https://read.qxmd.com/read/18656460/purification-and-mass-spectrometric-analysis-of-the-kappa-opioid-receptor
#40
JOURNAL ARTICLE
Kenneth M Wannemacher, Alexandra Terskiy, Shengjie Bian, Prem N Yadav, Hong Li, Richard D Howells
A clonal human embryonic kidney (HEK) 293 cell line was established that stably expressed the rat kappa-opioid receptor (rKOR) with a FLAG epitope at the amino terminus. The Kd for [3H]diprenorphine was 1.1+/-0.2 nM, and the Bmax was 2.6+/-0.4 pmol/mg. Dynorphin A (1-13), U69,593 and naloxone competitively inhibited [3H]diprenorphine binding with Ki values of 2.0, 18 and 18 nM, respectively, in good agreement with previously reported affinities for the unmodified receptor. U69,593 stimulated [35S]GTPgammaS binding in a concentration-dependent manner and caused phosphorylation of mitogen-activated protein (MAP) kinase, indicating that the activated epitope-tagged receptor triggered appropriate signaling pathways...
September 16, 2008: Brain Research
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