Publications by authors named "Abbas A Vafaei"

Corticosteroid signaling plays a critical role in modulating the neural systems underlying reward and addiction, but the specific contributions of glucocorticoid receptors (GRs) and mineralocorticoid receptors (MRs) in the medial prefrontal cortex (mPFC) to opioid reward and dopaminergic plasticity remain unclear. Here, we investigated the effects of intra-mPFC injection of corticosteroid receptor ligand (corticosterone; CORT), glucocorticoid receptor antagonist (RU38486; RU), and mineralocorticoid receptor antagonist (spironolactone; SP) on morphine-induced conditioned place preference (CPP) and dopamine transporter (DAT) expression in the mPFC. Adult male Wistar rats received intra-mPFC injections of CORT, RU, SP, or their respective vehicles prior to morphine CPP conditioning.

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Post-traumatic stress disorder (PTSD) is a challenging mental health condition that affects millions of people worldwide after they experience traumatic events. The current medications often do not fully address the wide range of PTSD symptoms or the underlying brain mechanisms, prompting the need to explore new treatments. Polyphenols, which are natural compounds found in many plant-based foods, have gained interest due to their brain-protective, anti-inflammatory, and antioxidant benefits.

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Memory retrieval involves recalling previously consolidated information, while memory extinction refers to the gradual weakening of such memories after recall. Stress and glucocorticoids influence the retrieval and extinction of memory. This study employed a passive avoidance task to examine the impact of acute mild stress and equivalent doses of exogenous corticosterone on fear memory retrieval and extinction in male mice.

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The purpose of this research was to assess the impact of different doses of Daphnetin (DAP, a natural compound derived from coumarin) on hippocampus neuronal injury, neurobehavioral function, blood-brain barrier (BBB) integrity, expression of claudin-5, brain-derived neurotrophic factor (BDNF), superoxide dismutase (SOD), and inflammatory markers in a mouse model of cerebral ischemia. Cerebral ischemia was induced in mice through 30 minutes of bilateral common carotid occlusion (BCCAO), followed by 48 hours of reperfusion. The viability of hippocampal neurons was assessed using Cresyl violet staining and BBB function was determined by measuring Evans blue (E.

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Purpose: The infralimbic (IL) subregion of the medial prefrontal cortex (mPFC) regulates the extinction of conditioned fear memory. Glucocorticoid and gamma-aminobutyric acid (GABA) receptors are expressed in the mPFC and are also critical in fear extinction. This study investigated the possible interactive effects of the glucocorticoids and GABAergic system in the IL on the regulation of fear extinction.

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Purpose: Levothyroxine (LEV) monotherapy cannot completely improve cognitive and behavioral impairments induced by hypothyroidism, whereas a combination therapy of exercise and LEV may ameliorate these deficits. This study aimed to determine the effects of mild-intensity forced exercise and LEV treatment on the anxiety profile and cognitive functions in male offspring of hypothyroid dams.

Method: Twenty-four female rats (mothers) were randomly divided into sham (healthy) and hypothyroidism groups and then placed with male rats to mate.

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The neuropeptide relaxin-3 and its cognate receptor, relaxin family peptide-3 receptors (RXFP3), have been implicated in modulating learning and memory processes, but their specific roles remain unclear. This study utilized behavioral and molecular approaches to investigate the effects of putatively reversible blockade of RXFP3 in the ventral dentate gyrus (vDG) of the hippocampus on spatial and fear memory formation in rats. Male Wistar rats received bilateral vDG cannula implantation and injections of the RXFP3 antagonist, R3(BΔ23-27)R/I5 (400 ng/0.

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  • Prenatal exposure to valproic acid (VPA) in rats increases the risk of autism-like behaviors in their offspring, which the study aimed to investigate using Prangos ferulacea as a potential treatment.!
  • Pregnant rats were given VPA or saline, and their pups received varying doses of Prangos ferulacea after birth, with behavioral tests conducted to evaluate the pups' responses at different ages.!
  • Results showed that Prangos ferulacea effectively reversed behavior changes and oxidative stress caused by VPA, suggesting its potential as a treatment to mitigate autism spectrum disorder symptoms. !
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Autism is a neurobehavioral disease that induces cognitive and behavioral alterations, usually accompanied by oxidative stress in the brain. Crocus sativus (saffron) and its active ingredient, crocin, have potent antioxidative effects that may benefit autistic behaviors. This study aimed to determine the effects of saffron extract and crocin against brain oxidative stress and behavioral, motor, and cognitive deficits in an animal model of autism in male offspring rats.

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Humans have lived in a dynamic environment fraught with potential dangers for thousands of years. While fear and stress were crucial for the survival of our ancestors, today, they are mostly considered harmful factors, threatening both our physical and mental health. Trauma is a highly stressful, often life-threatening event or a series of events, such as sexual assault, war, natural disasters, burns, and car accidents.

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Reconsolidation is an active process induced following the reactivation of previously consolidated memories. Recent studies suggest brain corticosteroid receptors may participate in the modulation of fear memory reconsolidation. Glucocorticoid receptors (GRs), with 10-fold lower affinity than mineralocorticoid receptors (MRs), are mainly occupied during the peak of the circadian rhythm, and after stress, so they probably have a more critical role than MRs in memory phases during stressful situations.

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This study investigated the interactive effect of glucocorticoid and β-adrenoceptors in the infralimbic (IL) cortex on the acquisition and consolidation of fear extinction in rats' auditory fear conditioning (AFC) task. On day 1, rats underwent habituation for 9 min (12 tones, 10 s, 4 kHz, 80 dB, without footshock). On day 2 (conditioning), rats received 3 mild electrical footshocks (US; 2 s, 0.

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Article Synopsis
  • This study explored how glucocorticoids and GABA receptors in the infralimbic cortex affect fear extinction in rats during an auditory fear conditioning task.
  • Rats were conditioned with tones and footshocks, followed by extinction trials after receiving corticosterone, which enhanced their ability to extinguish fear.
  • Co-administration of GABA antagonists blocked the effects of corticosterone, showing that glucocorticoid receptors and GABA receptors work together through the ERK pathway to modulate fear extinction.
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The extinction of auditory fear conditioning (AFC) refers to reducing the fear responses induced following repeated presentation of a conditioned stimulus (tone) in the absence of an unconditioned stimulus (electric foot shock). Glucocorticoid receptors (GRs) play an important role in extinction, but the underlying neurobiological mechanisms are unclear. This study aimed to investigate the interaction between glucocorticoids and β-adrenoceptors of the infra-limbic cortex (IL) in regulating the acquisition and consolidation of fear memory extinction in rats.

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Introduction: The basolateral amygdala (BLA) and infralimbic area (IL) of the medial prefrontal cortex (mPFC) are two interconnected brain structures that mediate both fear memory expression and extinction. Besides the well-known role of the BLA in the acquisition and expression of fear memory, projections from IL to BLA inhibit fear expression and have a critical role in fear extinction. However, the details of IL-BLA interaction have remained unclear.

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  • The study aimed to explore the effects of oxytocin (OXT) on neuronal damage and related molecular mechanisms in a mouse model of stroke induced by middle cerebral artery occlusion.
  • Results showed that OXT treatment significantly reduced brain injury and inflammation markers, as well as promoting protective brain proteins, although it did not improve neurological functions or memory.
  • The findings suggest that pre-stroke administration of OXT could have potential therapeutic benefits in limiting brain damage from strokes, indicating a possible new preventive treatment option for clinical use.
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  • Chronic morphine use negatively affects the ability to extinguish cued fear responses, potentially increasing the risk of anxiety disorders and relapse in opioid addiction.
  • Rats given chronic morphine showed impaired cued fear responses after fear conditioning, but forced exercise at light or moderate intensities helped improve their recovery by enhancing brain-derived neurotrophic factor (BDNF) levels.
  • The study suggests that moderate exercise can shift the balance between pro-apoptotic and anti-apoptotic proteins in the hippocampus, promoting cell survival and aiding in the rehabilitation of fear extinction impairments linked to chronic opioid use.
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  • Disruptions in the light/dark cycle negatively impact memory formation and retrieval in both humans and animals, particularly observed through animal studies.
  • A study involving adult male Wistar rats divided them into two groups: one with a normal light/dark cycle and another kept in constant darkness for three weeks, with performance measured using the Morris Water maze and auditory fear conditioning tests.
  • Rats in constant darkness showed impaired spatial memory retrieval and enhanced extinction of auditory fear memory during the light phase and had altered BDNF/TRKB protein levels in the hippocampus, indicating serious effects on their neural function compared to those in regular light/dark conditions.
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  • Fear extinction is crucial for treating psychiatric disorders, and oxytocin (OT) has been identified as a potential facilitator in this process.
  • The study found that endogenous OT levels significantly increase during fear extinction in the dorsal hippocampus (dHPC), suggesting it enhances the fear extinction process, especially when combined with BDNF.
  • OT's effects involve increased neural activity in critical brain regions, like the CA1-vHPC and the infralimbic cortex, underscoring the importance of the dHPC-mPFC pathway in fear extinction mechanisms.
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The present study was conducted to investigate the effects of different doses of recombinant human Chemerin (rhChemerin) on brain damage, spatial memory, blood-brain barrier (BBB) disruption and cellular and molecular mechanisms in a mouse stroke model. The mouse stroke model was developed by blocking the middle cerebral artery for 1 h and performing reperfusion for 23 h. Immediately, one and three hours after the stroke, 200, 400 and 800 ng/mouse of intranasal rhChemerin was administered.

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  • The study aimed to evaluate the effects of valerian on sleep quality, depression, and anxiety in patients undergoing hemodialysis (HD).
  • In a randomized trial with 39 participants, one group received valerian while the other received a placebo for a month, followed by a crossover to evaluate the opposite treatment after a washout period.
  • Results indicated that valerian significantly improved sleep quality, reduced state anxiety, and alleviated depression more effectively than the placebo in HD patients.
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Objectives: A few experimental studies have shown the therapeutic effects of oxytocin on focal cerebral ischemia. In this study, the prophylactic effect of intranasal oxytocin on brain damage was investigated in a cerebral ischemic model.

Materials And Methods: Intranasal oxytocin (8 IU/per mouse) was prescribed daily for one week.

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Introduction: of the study: Post-training administration of glucocorticoids enhance memory consolidation of inhibitory avoidance learning. Given the involvement of 5-HT6 receptors in memory processing and the interaction of glucocorticoids with the brain serotonergic system in modulating memory processing, we investigated whether the effect of glucocorticoids on the consolidation of emotionally arousing training depends on hippocampal 5-HT6 receptors.

Methods: Rats were trained in an inhibitory avoidance task and immediately received the systemic injections of corticosterone (CORT) as well as the intra-hippocampal injections of 5-HT receptors agonist or antagonist.

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