keyword
https://read.qxmd.com/read/38590677/molecular-docking-mm-gbsa-and-molecular-dynamics-approach-5-meo-dmt-analogues-as-potential-antidepressants
#21
JOURNAL ARTICLE
Rajagopal Kalirajan, Khare Rishabh, Jupudi Srikanth, Modi Niharika, Negi Preeya, Islam Rezaul
Since depression is a common mental illness affecting an estimated 5% of people worldwide, investigators are encouraged to develop effective antidepressants. According to the monoamine-deficiency hypothesis, the underlying pathophysiology of depression is a deficiency of some neurotransmitters (serotonin, norepinephrine, or dopamine) in the central nervous system. The neurotransmitter serotonin has drawn the most attention concerning depression. As per research, 5-methoxy-N, N-dimethyltryptamine (5-MeO-DMT) elevates inter-synaptic serotonin levels when administered as a single inhalation of vapor from dried toad secretion and leads to higher life satisfaction, convergent thinking, higher ratings of mindfulness, lower ratings of depression, and anxiety...
October 2023: Archives of Razi Institute
https://read.qxmd.com/read/38586193/the-impact-of-estradiol-on-serotonin-glutamate-and-dopamine-systems
#22
REVIEW
Peyton Christine Bendis, Sydney Zimmerman, Anna Onisiforou, Panos Zanos, Polymnia Georgiou
Estradiol, the most potent and prevalent member of the estrogen class of steroid hormones and is expressed in both sexes. Functioning as a neuroactive steroid, it plays a crucial role in modulating neurotransmitter systems affecting neuronal circuits and brain functions including learning and memory, reward and sexual behaviors. These neurotransmitter systems encompass the serotonergic, dopaminergic, and glutamatergic signaling pathways. Consequently, this review examines the pivotal role of estradiol and its receptors in the regulation of these neurotransmitter systems in the brain...
2024: Frontiers in Neuroscience
https://read.qxmd.com/read/38583575/a-novel-peptide-drug-conjugate-for-glioma-targeted-drug-delivery
#23
JOURNAL ARTICLE
Jianfen Zhou, Nana Meng, Linwei Lu, Jiasheng Lu, Sunyi Wu, Yuan Ding, Shuai Wu, Yanning Bao, Qianzhu Xu, Ruohan Chen, Jun Wang, Cao Xie, Jinsong Wu, Weiyue Lu
The existence of the blood-brain barrier (BBB) and blood-brain tumor barrier (BBTB) greatly limits the application of chemotherapy in glioma. To address this challenge, an optimal drug delivery system must efficiently cross the BBB/BBTB and specifically deliver therapeutic drugs into glioma cells while minimizing systemic toxicity. Here we demonstrated that glucose-regulated protein 78 (GRP78) and dopamine receptor D2 were highly expressed in patient-derived glioma tissues, and dopamine receptors were highly expressed on the BBB...
April 5, 2024: Journal of Controlled Release
https://read.qxmd.com/read/38580732/disruption-of-positive-and-negative-feature-morphine-interoceptive-occasion-setters-by-dopamine-receptor-agonism-and-antagonism-in-male-and-female-rats
#24
JOURNAL ARTICLE
Davin R Peart, Caitlin J Nolan, Adiia P Stone, Mckenna A Williams, Jessica M Karlovcec, Jennifer E Murray
RATIONALE: Internally perceived stimuli evoked by morphine administration can form Pavlovian associations such that they can function as occasion setters (OSs) for externally perceived reward cues in rats, coming to modulate reward-seeking behaviour. Though much research has investigated mechanisms underlying opioid-related reinforcement and analgesia, neurotransmitter systems involved in the functioning of opioids as Pavlovian interoceptive discriminative stimuli remain to be disentangled despite documented differences in the development of tolerance to analgesic versus discriminative stimulus effects...
April 6, 2024: Psychopharmacology
https://read.qxmd.com/read/38575350/pharmacological-inhibition-of-the-nucleus-accumbens-increases-dyadic-social-interaction-in-macaques
#25
JOURNAL ARTICLE
Hannah F Waguespack, Jessica T Jacobs, Janis Park, Carolina Campos-Rodriguez, Rafael S Maior, Patrick A Forcelli, Ludise Malkova
The nucleus accumbens (NAc) is a central component of the brain circuitry that mediates motivated behavior, including reward processing. Since the rewarding properties of social stimuli have a vital role in guiding behavior (both in humans and nonhuman animals), the nucleus accumbens is likely to contribute to the brain circuitry controlling social behavior. In rodents, prior studies have found that focal pharmacological inhibition of NAc and/or elevation of dopamine in NAc increases social interactions. However, the role of the NAc in social behavior in nonhuman primates remains unknown...
April 4, 2024: ENeuro
https://read.qxmd.com/read/38572143/neural-mechanisms-of-dopamine-function-in-learning-and-memory-in-caenorhabditis-elegans
#26
REVIEW
Anna McMillen, Yee Lian Chew
Research into learning and memory over the past decades has revealed key neurotransmitters that regulate these processes, many of which are evolutionarily conserved across diverse species. The monoamine neurotransmitter dopamine is one example of this, with countless studies demonstrating its importance in regulating behavioural plasticity. However, dopaminergic neural networks in the mammalian brain consist of hundreds or thousands of neurons, and thus cannot be studied at the level of single neurons acting within defined neural circuits...
January 2024: Neuronal Signaling
https://read.qxmd.com/read/38567902/stimulation-of-vta-dopamine-inputs-to-lh-upregulates-orexin-neuronal-activity-in-a-drd2-dependent-manner
#27
JOURNAL ARTICLE
Masaya Harada, Laia Serratosa Capdevila, Maria Wilhelm, Denis Burdakov, Tommaso Patriarchi
Dopamine and orexins (hypocretins) play important roles in regulating reward-seeking behaviors. It is known that hypothalamic orexinergic neurons project to dopamine neurons in the ventral tegmental area (VTA), where they can stimulate dopaminergic neuronal activity. Although there are reciprocal connections between dopaminergic and orexinergic systems, whether and how dopamine regulates the activity of orexin neurons is currently not known. Here we implemented an opto-Pavlovian task in which mice learn to associate a sensory cue with optogenetic dopamine neuron stimulation to investigate the relationship between dopamine release and orexin neuron activity in the lateral hypothalamus (LH)...
April 3, 2024: ELife
https://read.qxmd.com/read/38567425/skf82958-a-dopamine-d1-receptor-agonist-disrupts-prepulse-inhibition-in-the-medial-prefrontal-cortex-and-nucleus-accumbens-in-c57bl-6j-mice
#28
JOURNAL ARTICLE
Chengmei Yang, Xiaoyu Chen, Jingyang Xu, Weihai Chen
Prepulse inhibition (PPI) is a crucial indicator of sensorimotor gating that is often impaired in neuropsychiatric diseases. Although dopamine D1 receptor agonists have been found to disrupt PPI in mice, the underlying mechanisms are not fully understood. In this study, we aimed to identify the brain regions responsible for the PPI-disruptive effect of the D1 agonist in mice. Results demonstrated that intraperitoneal administration of the selective dopamine D1 receptor agonist SKF82958 dramatically inhibited PPI, while the dopamine D1 receptor antagonist SCH23390 enhanced PPI...
March 29, 2024: Behavioural Pharmacology
https://read.qxmd.com/read/38565057/inhibition-of-calcium-sensing-receptor-by-its-antagonist-promotes-gastrointestinal-motility-in-a-parkinson-s-disease-mouse-model
#29
JOURNAL ARTICLE
Yu-Hang Li, Zhong-Xin Jiang, Qian Xu, Ting-Ting Jin, Jin-Fang Huang, Xiao Luan, Chong Li, Xin-Yi Chen, Ka-Hing Wong, Xiao-Li Dong, Xiang-Rong Sun
BACKGROUND: The Calcium-sensing receptor (CaSR) participates in the regulation of gastrointestinal (GI) motility under normal conditions and might be involved in the regulation of GI dysmotility in patients with Parkinson's disease (PD). METHODS: CaSR antagonist-NPS-2143 was applied in in vivo and ex vivo experiments to study the effect and underlying mechanisms of CaSR inhibition on GI dysmotility in the MPTP-induced PD mouse model. FINDINGS: Oral intake of NPS-2143 promoted GI motility in PD mice as shown by the increased gastric emptying rate and shortened whole gut transit time together with improved weight and water content in the feces of PD mice, and the lack of influence on normal mice...
April 1, 2024: Biomedicine & Pharmacotherapy
https://read.qxmd.com/read/38563864/dpp-4-inhibitors-sitagliptin-and-pf-00734-200-mitigate-dopaminergic-neurodegeneration-neuroinflammation-and-behavioral-impairment-in-the-rat-6-ohda-model-of-parkinson-s-disease
#30
JOURNAL ARTICLE
Seong-Jin Yu, Yun Wang, Hui Shen, Eun-Kyung Bae, Yazhou Li, Kumar Sambamurti, Michael A Tones, Margaret M Zaleska, Barry J Hoffer, Nigel H Greig
Epidemiological studies report an elevated risk of Parkinson's disease (PD) in patients with type 2 diabetes mellitus (T2DM) that is mitigated in those prescribed dipeptidyl peptidase 4 (DPP-4) inhibitors. With an objective to characterize clinically translatable doses of DPP-4 inhibitors (gliptins) in a well-characterized PD rodent model, sitagliptin, PF-00734,200 or vehicle were orally administered to rats initiated either 7-days before or 7-days after unilateral medial forebrain bundle 6-hydroxydopamine (6-OHDA) lesioning...
April 2, 2024: GeroScience
https://read.qxmd.com/read/38563661/activation-of-mglu2-3-receptors-with-the-orthosteric-agonist-ly-404-039-alleviates-dyskinesia-in-experimental-parkinsonism
#31
JOURNAL ARTICLE
Woojin Kang, Imane Frouni, Cynthia Kwan, Louis Desbiens, Adjia Hamadjida, Philippe Huot
LY-404,039 is an orthosteric agonist at metabotropic glutamate 2 and 3 (mGlu2/3) receptors, with a possible additional agonist effect at dopamine D2 receptors. LY-404,039 and its pro-drug, LY-2140023, have previously been tested in clinical trials for psychiatric indications and could therefore be repurposed if they were shown to be efficacious in other conditions. We have recently demonstrated that the mGlu2/3 orthosteric agonist LY-354,740 alleviated L-3,4-dihydroxyphenylalanine (L-DOPA)-induced abnormal involuntary movements (AIMs) in the 6-hydroxydopamine (6-OHDA)-lesioned rat without hampering the anti-parkinsonian action of L-DOPA...
March 29, 2024: Behavioural Pharmacology
https://read.qxmd.com/read/38561086/1-phenylselanyl-2-p-tolyl-indolizine-a-selenoindolizine-with-potential-antidepressant-like-activity-in-mice-mediated-by-the-modulation-of-dopaminergic-and-noradrenergic-systems
#32
JOURNAL ARTICLE
Marcia Juciele da Rocha, Marcelo Heinemann Presa, Gustavo D'Avila Nunes, Narryman Pinto Zuge, Camila Simões Pires, Evelyn Mianes Besckow, Caroline Signorini Gomes, Luiz Henrique Dapper, Eder João Lenardão, Filipe Penteado, Cristiani Folharini Bortolatto, César Augusto Brüning
1-(Phenylselanyl)-2-(p-tolyl)indolizine (MeSeI) is a selenoindolizine with an antidepressant-like effect in mice by regulation of the serotonergic system. This study investigated the involvement of dopaminergic and noradrenergic systems in the antidepressant-like action of MeSeI. For this purpose, Swiss male mice were pretreated with different antagonists, after 15 min, the MeSeI was administrated by intragastric (i.g.) via; after 30 min, the mouse behavior was assessed in the forced swimming test (FST)...
March 30, 2024: Brain Research
https://read.qxmd.com/read/38555117/alcohol-and-the-dopamine-system
#33
JOURNAL ARTICLE
Bo Söderpalm, Mia Ericson
The mesolimbic dopamine pathway plays a major role in drug reinforcement and is likely involved also in the development of drug addiction. Ethanol, like most addictive drugs, acutely activates the mesolimbic dopamine system and releases dopamine, and ethanol-associated stimuli also appear to trigger dopamine release. In addition, chronic exposure to ethanol reduces the baseline function of the mesolimbic dopamine system. The molecular mechanisms underlying ethanol´s interaction with this system remain, however, to be unveiled...
2024: International Review of Neurobiology
https://read.qxmd.com/read/38555114/current-treatments-of-alcohol-use-disorder
#34
JOURNAL ARTICLE
Tommaso Dionisi, Giovanna Di Sario, Lorenzo De Mori, Giorgia Spagnolo, Mariangela Antonelli, Claudia Tarli, Luisa Sestito, Francesco Antonio Mancarella, Daniele Ferrarese, Antonio Mirijello, Gabriele Angelo Vassallo, Antonio Gasbarrini, Giovanni Addolorato
Emerging treatments for alcohol dependence reveal an intricate interplay of neurobiological, psychological, and circumstantial factors that contribute to Alcohol Use Disorder (AUD). The approved strategies balancing these factors involve extensive manipulations of neurotransmitter systems such as GABA, Glutamate, Dopamine, Serotonin, and Acetylcholine. Innovative developments are engaging mechanisms such as GABA reuptake inhibition and allosteric modulation. Closer scrutiny is placed on the role of Glutamate in chronic alcohol consumption, with treatments like NMDA receptor antagonists and antiglutamatergic medications showing significant promise...
2024: International Review of Neurobiology
https://read.qxmd.com/read/38554797/unveiling-the-therapeutic-prospects-of-egfr-inhibition-in-rotenone-mediated-parkinsonism-in-rats-modulation-of-dopamine-d3-receptor
#35
JOURNAL ARTICLE
Heba M Mansour, Ahmed F Mohamed, Mahmoud M Khattab, Aiman S El-Khatib
Parkinson's disease (PD) is characterized by the progressive loss of dopaminergic neurons in the substantia nigra. The dopamine D3 receptor (D3R) plays a significant role in the pathogenesis and treatment of PD. Activation of receptor tyrosine kinases (RTKs) inhibits signaling mediated by G protein-coupled receptor (GPCR). Epidermal growth factor receptors (EGFRs) and dopamine D3 receptors in the brain are directly associated with PD, both in terms of its development and potential treatment. Therefore, we investigated the impact of modulating the EGFR, a member of the RTKs family, and the dopamine D3R, a member of the GPCR family...
March 28, 2024: Brain Research
https://read.qxmd.com/read/38549620/synthetic-exendin-4-disrupts-responding-to-reward-predictive-incentive-cues-in-male-rats
#36
JOURNAL ARTICLE
Ken T Wakabayashi, Ajay N Baindur, Malte Feja, Mauricio Suarez, Karie Chen, Kimberly Bernosky-Smith, Caroline E Bass
Synthetic exendin-4 (EX4, exenatide), is a GLP-1 receptor agonist used clinically to treat glycemia in Type-2 diabetes mellitus. EX4 also promotes weight loss and alters food reward-seeking behaviors in part due to activation of GLP-1 receptors in the mesolimbic dopamine system. Evidence suggests that GLP-1 receptor activity can directly attenuate cue-induced reward seeking. Here, we tested the effects of EX4 (0.6, 1.2, and 2.4 μg/kg, i.p.) on incentive cue (IC) responding, using a task where rats emit a nosepoke response during an intermittent reward-predictive IC to obtain a sucrose reward...
2024: Frontiers in Behavioral Neuroscience
https://read.qxmd.com/read/38532011/active-forgetting-and-neuropsychiatric-diseases
#37
REVIEW
Jacob A Berry, Dana C Guhle, Ronald L Davis
Recent and pioneering animal research has revealed the brain utilizes a variety of molecular, cellular, and network-level mechanisms used to forget memories in a process referred to as "active forgetting". Active forgetting increases behavioral flexibility and removes irrelevant information. Individuals with impaired active forgetting mechanisms can experience intrusive memories, distressing thoughts, and unwanted impulses that occur in neuropsychiatric diseases. The current evidence indicates that active forgetting mechanisms degrade, or mask, molecular and cellular memory traces created in synaptic connections of "engram cells" that are specific for a given memory...
March 26, 2024: Molecular Psychiatry
https://read.qxmd.com/read/38530646/lesion-network-of-oculogyric-crises-maps-to-brain-dopaminergic-transcriptomic-signature
#38
JOURNAL ARTICLE
Bassam Al-Fatly, Clemens Neudorfer, Diego Kaski, Anthony E Lang, Andrea A Kühn, Michael D Fox, Andreas Horn, Christos Ganos
Oculogyric crises are acute episodes of sustained, typically upward, conjugate deviation of the eyes. Oculogyric crises usually occur as the result of acute D2-dopamine receptor blockade, but the brain areas causally involved in generating this symptom remain elusive. Here, we used data from 14 previously reported cases of lesion-induced oculogyric crises and employed lesion network mapping to identify their shared connections throughout the brain. This analysis yielded a common network that included basal ganglia, thalamic, and brainstem nuclei, as well as the cerebellum...
March 26, 2024: Brain
https://read.qxmd.com/read/38529497/development-of-novel-tools-for-dissection-of-central-versus-peripheral-dopamine-d-2-like-receptor-signaling-in-dysglycemia
#39
Alessandro Bonifazi, Michael Ellenberger, Zachary J Farino, Despoina Aslanoglou, Rana Rais, Sandra Pereira, José O Mantilla-Rivas, Comfort A Boateng, Amy J Eshleman, Aaron Janowsky, Margaret K Hahn, Gary J Schwartz, Barbara S Slusher, Amy Hauck Newman, Zachary Freyberg
Dopamine (DA) D 2 -like receptors in both the central nervous system (CNS) and the periphery are key modulators of metabolism. Moreover, disruption of D 2 -like receptor signaling is implicated in dysglycemia. Yet, the respective metabolic contributions of CNS versus peripheral D 2 -like receptors including D 2 (D2R) and D 3 (D3R) receptors remain poorly understood. To address this, we developed new pharmacological tools, D 2 -like receptor agonists with diminished and delayed blood-brain barrier capability, to selectively manipulate D2R/D3R signaling in the periphery...
February 24, 2024: bioRxiv
https://read.qxmd.com/read/38528956/activation-of-nucleus-accumbens-projections-to-the-ventral-tegmental-area-alters-molecular-signaling-and-neurotransmission-in-the-reward-system
#40
JOURNAL ARTICLE
Alaa Khayat, Rami Yaka
The nucleus accumbens (NAc) and the ventral tegmental area (VTA) are integral brain regions involved in reward processing and motivation, including responses to drugs of abuse. Previously, we have demonstrated that activation of NAc-VTA afferents during the acquisition of cocaine conditioned place preference (CPP) reduces the rewarding properties of cocaine and diminished the activity of VTA dopamine neurons. In the current study, we examined the impact of enhancing these inhibitory inputs on molecular changes and neurotransmission associated with cocaine exposure...
2024: Frontiers in Molecular Neuroscience
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