Pub Date : 2025-12-13DOI: 10.1016/j.physbeh.2025.115206
Rebecca M. Craft, Alexa R. Calvert, Faith Spencer, Michael M. Morgan
Health-related organizations have called for broadening biomedical research to include gender-diverse individuals. The present study tested the validity of an animal model of gender affirming testosterone therapy that may be useful for determining the impact of hormonal transition on a variety of health outcomes in both adolescents and adults. Blank or testosterone-filled capsules were implanted s.c. into gonadally intact adolescent (post-natal day 43) and adult (post-natal day 92) female rats. Body weight, estrous cycling, and home cage wheel running were recorded for 3 weeks; other physiological indices of defeminization and masculinization were assessed 29–30 days after capsule implantation. Testosterone treatment at male-typical levels suppressed estrous cycling and uterine weight, increased body weight and lean mass, and increased low density lipoprotein levels in both adolescents and adults. Testosterone increased clitoral gland size in adolescents. In contrast, wheel running was not significantly altered by testosterone. Results suggest that testosterone exposure at male-typical levels in gonadally intact female rats – whether adolescent or adult at the initiation of treatment – is a valid model of gender affirming testosterone therapy in terms of hormone impact on a variety of physiological measures. This model can thus provide a clinically relevant avenue for advancing transgender medicine.
{"title":"Continuous testosterone exposure alters body weight, lean mass, estrous cycling and lipid profile, but not wheel running in adolescent or adult female rats","authors":"Rebecca M. Craft, Alexa R. Calvert, Faith Spencer, Michael M. Morgan","doi":"10.1016/j.physbeh.2025.115206","DOIUrl":"10.1016/j.physbeh.2025.115206","url":null,"abstract":"<div><div>Health-related organizations have called for broadening biomedical research to include gender-diverse individuals. The present study tested the validity of an animal model of gender affirming testosterone therapy that may be useful for determining the impact of hormonal transition on a variety of health outcomes in both adolescents and adults. Blank or testosterone-filled capsules were implanted s.c. into gonadally intact adolescent (post-natal day 43) and adult (post-natal day 92) female rats. Body weight, estrous cycling, and home cage wheel running were recorded for 3 weeks; other physiological indices of defeminization and masculinization were assessed 29–30 days after capsule implantation. Testosterone treatment at male-typical levels suppressed estrous cycling and uterine weight, increased body weight and lean mass, and increased low density lipoprotein levels in both adolescents and adults. Testosterone increased clitoral gland size in adolescents. In contrast, wheel running was not significantly altered by testosterone. Results suggest that testosterone exposure at male-typical levels in gonadally intact female rats – whether adolescent or adult at the initiation of treatment – is a valid model of gender affirming testosterone therapy in terms of hormone impact on a variety of physiological measures. This model can thus provide a clinically relevant avenue for advancing transgender medicine.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"305 ","pages":"Article 115206"},"PeriodicalIF":2.5,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145763434","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Endocannabinoid (eCB) systems have been implicated in the development of stress-induced anxiety. In this study, we investigated the changes in eCB levels in the mouse brain due to restraint stress. In addition, we examined the effects of eCB-degrading enzyme inhibitors on anxiety-like behavior in restraint-stressed mice. For restraint stress, the mice were immobilized in a 50 ml syringe with holes for airflow for 30 min. After restraint stress, the contents of 2-arachidonoylglycerol (2-AG) and N-arachidonoylethanolamine (AEA) were measured via UPLC‒MS/MS. Immediately after restraint stress, 2-AG content was significantly decreased in the prefrontal cortex (PFC) and hippocampus (HC). Similarly, AEA content was decreased in the PFC and HC, although 2-AG and AEA contents did not change in the striatum, periamygdaloid cortex or medulla oblongata. On the other hand, at both 30 and 60 min after restraint stress, 2-AG content was significantly increased in the PFC and HC. However, AEA content remained reduced in the PFC for up to 30 min after stress exposure, but the significant reduction was no longer observed at 60 min. In the elevated plus-maze test, the time spent in the open arms decreased in restraint-stressed mice, which indicated the occurrence of anxiogenic behavior. This anxiogenic behavior was ameliorated by the administration of JZL184 (a monoacylglycerol lipase inhibitor) or URB597. (a fatty acid amide hydrolase inhibitor) These results suggest that eCB levels are highly responsive to time-dependent and brain region-specific changes in response to acute stress stimuli. Furthermore, restraint stress induces anxiogenic behavior, which is ameliorated by inhibitors of eCB-degrading enzymes. These findings indicate that the reduction in eCB levels in the PFC and HC may be due to the development of stress-induced anxiety.
{"title":"Alteration of brain endocannabinoids on restraint stress-induced anxiety-like behaviors in mice","authors":"Ryo Fukumori, Kanan Ueo, Ryosuke Nakashima, Taku Yamaguchi","doi":"10.1016/j.physbeh.2025.115201","DOIUrl":"10.1016/j.physbeh.2025.115201","url":null,"abstract":"<div><div>Endocannabinoid (eCB) systems have been implicated in the development of stress-induced anxiety. In this study, we investigated the changes in eCB levels in the mouse brain due to restraint stress. In addition, we examined the effects of eCB-degrading enzyme inhibitors on anxiety-like behavior in restraint-stressed mice. For restraint stress, the mice were immobilized in a 50 ml syringe with holes for airflow for 30 min. After restraint stress, the contents of 2-arachidonoylglycerol (2-AG) and <em>N</em>-arachidonoylethanolamine (AEA) were measured via UPLC‒MS/MS. Immediately after restraint stress, 2-AG content was significantly decreased in the prefrontal cortex (PFC) and hippocampus (HC). Similarly, AEA content was decreased in the PFC and HC, although 2-AG and AEA contents did not change in the striatum, periamygdaloid cortex or medulla oblongata. On the other hand, at both 30 and 60 min after restraint stress, 2-AG content was significantly increased in the PFC and HC. However, AEA content remained reduced in the PFC for up to 30 min after stress exposure, but the significant reduction was no longer observed at 60 min. In the elevated plus-maze test, the time spent in the open arms decreased in restraint-stressed mice, which indicated the occurrence of anxiogenic behavior. This anxiogenic behavior was ameliorated by the administration of JZL184 (a monoacylglycerol lipase inhibitor) or URB597. (a fatty acid amide hydrolase inhibitor) These results suggest that eCB levels are highly responsive to time-dependent and brain region-specific changes in response to acute stress stimuli. Furthermore, restraint stress induces anxiogenic behavior, which is ameliorated by inhibitors of eCB-degrading enzymes. These findings indicate that the reduction in eCB levels in the PFC and HC may be due to the development of stress-induced anxiety.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"305 ","pages":"Article 115201"},"PeriodicalIF":2.5,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-11DOI: 10.1016/j.physbeh.2025.115203
Diego Fernández-Lázaro , Manuel Garrosa , Gema Santamaría , Enrique Roche , José María Izquierdo , Jesús Seco-Calvo , Juan Mielgo-Ayuso
Background
The influence of sexual activity prior to exercise on athletic performance remains controversial. While pre-competition abstinence is commonly advised, scientific evidence on its physiological impact is limited and inconsistent.
Methods
A randomized crossover study was conducted in 21 well-trained male athletes (age 22 ± 1 y) to compare the acute effects of masturbation-induced orgasm versus sexual abstinence performed 30 min before testing. Each participant completed an incremental cycling test and an isometric handgrip strength test under both conditions. Blood samples were analyzed for muscle damage (CK, LDH, Mb), inflammatory (CRP, IL-6), and hormonal (testosterone, cortisol, LH) markers.
Results
Compared with abstinence, the post-masturbation condition resulted in a longer exercise duration (+3.2%, p< 0.01) and higher heart rate (p< 0.001), accompanied by a small increase in mean handgrip strength (p< 0.05). Lower plasma LDH levels (p< 0.001) indicated reduced muscle stress. Testosterone and cortisol concentrations were significantly higher (both p< 0.001), whereas inflammatory markers (CRP, IL-6) showed no significant change.
Conclusions
Masturbation 30 min before exercise elicited mild sympathetic and hormonal activation without detrimental effects on performance or muscle damage. These findings suggest that pre-exercise sexual activity does not impair athletic capacity in trained men, challenging the long-standing myth of mandatory abstinence before competition.
{"title":"Sexual activity before exercise influences physiological response and sports performance in high-level trained men athletes","authors":"Diego Fernández-Lázaro , Manuel Garrosa , Gema Santamaría , Enrique Roche , José María Izquierdo , Jesús Seco-Calvo , Juan Mielgo-Ayuso","doi":"10.1016/j.physbeh.2025.115203","DOIUrl":"10.1016/j.physbeh.2025.115203","url":null,"abstract":"<div><h3>Background</h3><div>The influence of sexual activity prior to exercise on athletic performance remains controversial. While pre-competition abstinence is commonly advised, scientific evidence on its physiological impact is limited and inconsistent.</div></div><div><h3>Methods</h3><div>A randomized crossover study was conducted in 21 well-trained male athletes (age 22 ± 1 y) to compare the acute effects of masturbation-induced orgasm versus sexual abstinence performed 30 min before testing. Each participant completed an incremental cycling test and an isometric handgrip strength test under both conditions. Blood samples were analyzed for muscle damage (CK, LDH, Mb), inflammatory (CRP, IL-6), and hormonal (testosterone, cortisol, LH) markers.</div></div><div><h3>Results</h3><div>Compared with abstinence, the post-masturbation condition resulted in a longer exercise duration (+3.2%, <em>p</em>< 0.01) and higher heart rate (<em>p</em>< 0.001), accompanied by a small increase in mean handgrip strength (<em>p</em>< 0.05). Lower plasma LDH levels (<em>p</em>< 0.001) indicated reduced muscle stress. Testosterone and cortisol concentrations were significantly higher (both <em>p</em>< 0.001), whereas inflammatory markers (CRP, IL-6) showed no significant change.</div></div><div><h3>Conclusions</h3><div>Masturbation 30 min before exercise elicited mild sympathetic and hormonal activation without detrimental effects on performance or muscle damage. These findings suggest that pre-exercise sexual activity does not impair athletic capacity in trained men, challenging the long-standing myth of mandatory abstinence before competition.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"307 ","pages":"Article 115203"},"PeriodicalIF":2.5,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752085","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-11DOI: 10.1016/j.physbeh.2025.115202
Tian Tian , Yang Wang , Xu Xu , Jing Li , Jingbo Feng , Youfang Hu , Jirong Qi
Attention deficit hyperactivity disorder (ADHD), a highly prevalent neurodevelopmental disorder affecting children, presents with core symptoms of inattention, hyperactivity, and impulsivity, along with frequent comorbid learning and memory dysfunction. Emerging evidence implicates hippocampal dysfunction in ADHD-related learning and memory deficits, with brain-specific angiogenesis inhibitor 1-associated protein 2 (BAIAP2) emerging as a critical molecular player. While BAIAP2 has been independently associated with synaptic plasticity and ADHD pathogenesis, its specific role in ADHD-associated learning and memory impairment remains unexplored.
Using spontaneously hypertensive rats (SHR), we demonstrated significantly reduced hippocampal BAIAP2 expression compared to controls. Notably, methylphenidate (MPH) treatment increased BAIAP2 levels, while targeted BAIAP2 overexpression rescued learning and memory deficits, as evidenced by Morris water maze (MWM) performance. Furthermore, we preliminarily explored the possible regulatory interactions between BAIAP2 and the long non-coding RNA lncNONRATT002035.2.
These findings establish BAIAP2 as a pivotal mediator of hippocampal-dependent learning and memory dysfunction in ADHD and uncovered new aspects of disease pathology and potential targets for therapy.The newly discovered lncNONRATT002035.2-BAIAP2 axis warrants further investigation to elucidate its pathophysiological significance.
{"title":"Preliminary exploration of the role and mechanism of BAIAP2 in learning and memory impairment in ADHD","authors":"Tian Tian , Yang Wang , Xu Xu , Jing Li , Jingbo Feng , Youfang Hu , Jirong Qi","doi":"10.1016/j.physbeh.2025.115202","DOIUrl":"10.1016/j.physbeh.2025.115202","url":null,"abstract":"<div><div>Attention deficit hyperactivity disorder (ADHD), a highly prevalent neurodevelopmental disorder affecting children, presents with core symptoms of inattention, hyperactivity, and impulsivity, along with frequent comorbid learning and memory dysfunction. Emerging evidence implicates hippocampal dysfunction in ADHD-related learning and memory deficits, with brain-specific angiogenesis inhibitor 1-associated protein 2 (BAIAP2) emerging as a critical molecular player. While BAIAP2 has been independently associated with synaptic plasticity and ADHD pathogenesis, its specific role in ADHD-associated learning and memory impairment remains unexplored.</div><div>Using spontaneously hypertensive rats (SHR), we demonstrated significantly reduced hippocampal BAIAP2 expression compared to controls. Notably, methylphenidate (MPH) treatment increased BAIAP2 levels, while targeted BAIAP2 overexpression rescued learning and memory deficits, as evidenced by Morris water maze (MWM) performance. Furthermore, we preliminarily explored the possible regulatory interactions between BAIAP2 and the long non-coding RNA lncNONRATT002035.2.</div><div>These findings establish BAIAP2 as a pivotal mediator of hippocampal-dependent learning and memory dysfunction in ADHD and uncovered new aspects of disease pathology and potential targets for therapy.The newly discovered lncNONRATT002035.2-BAIAP2 axis warrants further investigation to elucidate its pathophysiological significance.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"306 ","pages":"Article 115202"},"PeriodicalIF":2.5,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145743927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-11DOI: 10.1016/j.physbeh.2025.115204
Xiao-Yan Huang , Nian-Nian Wang , Jing Zhou , Rui Su , Hao Li , Hai-Lin Ma , Ming Liu , De-Long Zhang
Indigenous Tibetans have developed documented physiological and neuroanatomical adaptations to high-altitude environments. However, the functional dynamics of their cognitive processing at such altitudes remain poorly characterized. To address this gap, we employed a visual search paradigm with high-temporal-resolution electroencephalography (EEG) to examine stimulus-driven attention (SDA) and goal-directed attention (GDA) in high-altitude Tibetans, with sea-level Han participants as a comparison group. Tibetans exhibited a “slow but steady” attentional pattern: despite longer reaction times (RTs), accuracy remained high (>95 %) and was comparable to that of Han controls in both attention types. This behavioral pattern in the Tibetan group was accompanied by distinctive late‑stage neural dynamics, reflected by smaller late positive potential (LPP) and late posterior negativity (LPN) and by lower theta‑band (4 - 10 Hz) event-related synchronization (ERS) during SDA, as well as smaller LPP during GDA. Source localization of the effects observed in these event-related potential (ERP) components and theta‑band ERS indicated predominant involvement of posterior midline and control-related regions in Han participants, whereas Tibetans showed greater engagement of motor‑related regions. These findings likely reflect an energy-efficient cognitive strategy for high-altitude adaptation. This study refines understanding of cognitive plasticity in extreme environments and provides electrophysiological foundations to inform interventions for high-altitude populations.
{"title":"An energy-efficient cognitive strategy? Neurophysiological dynamics of “slow but steady” attention in high-altitude Tibetans","authors":"Xiao-Yan Huang , Nian-Nian Wang , Jing Zhou , Rui Su , Hao Li , Hai-Lin Ma , Ming Liu , De-Long Zhang","doi":"10.1016/j.physbeh.2025.115204","DOIUrl":"10.1016/j.physbeh.2025.115204","url":null,"abstract":"<div><div>Indigenous Tibetans have developed documented physiological and neuroanatomical adaptations to high-altitude environments. However, the functional dynamics of their cognitive processing at such altitudes remain poorly characterized. To address this gap, we employed a visual search paradigm with high-temporal-resolution electroencephalography (EEG) to examine stimulus-driven attention (SDA) and goal-directed attention (GDA) in high-altitude Tibetans, with sea-level Han participants as a comparison group. Tibetans exhibited a “slow but steady” attentional pattern: despite longer reaction times (RTs), accuracy remained high (>95 %) and was comparable to that of Han controls in both attention types. This behavioral pattern in the Tibetan group was accompanied by distinctive late‑stage neural dynamics, reflected by smaller late positive potential (LPP) and late posterior negativity (LPN) and by lower theta‑band (4 - 10 Hz) event-related synchronization (ERS) during SDA, as well as smaller LPP during GDA. Source localization of the effects observed in these event-related potential (ERP) components and theta‑band ERS indicated predominant involvement of posterior midline and control-related regions in Han participants, whereas Tibetans showed greater engagement of motor‑related regions. These findings likely reflect an energy-efficient cognitive strategy for high-altitude adaptation. This study refines understanding of cognitive plasticity in extreme environments and provides electrophysiological foundations to inform interventions for high-altitude populations.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"305 ","pages":"Article 115204"},"PeriodicalIF":2.5,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752099","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-09DOI: 10.1016/j.physbeh.2025.115200
Sarra Miladi , Omar Hammouda , Samar J. Miladi Trabelsi , Sirine C. Miladi , Ranya Ameur , Tarak Driss
To evaluate the combined effect of physical activity (PA) and time-restricted eating (TRE) at different times of day (early (ETRE) versus late (LTRE) TRE) on eating behavior, cognitive performance, and cardiovascular parameters in women living with overweight or obesity.
Sixty one women were randomized into four groups: ETRE combined with PA (ETRE-PA, n = 15, 31.8 ± 10.76 years, 89.68 ± 13.40 kg, 33.5 ± 5.53 kg/m²), LTRE combined with PA (LTRE-PA, n = 15, 30.60 ± 7.94 years, 94.45 ± 15.36 kg, 34.37 ± 7.09 kg/m²), LTRE alone (LTRE, n = 15, 27.93 ± 9.79 years, 88.32 ± 10.36 kg, 32.71 ± 5.15 kg/m²) and a control group (CG, n = 16, 36.25 ± 11.52 years, 89.01 ± 11.68 kg, 33.66 ± 6.18 kg/m²).
In the post-intervention assessment (T1), ETRE-PA showed a significant reduction in eating disorder global scores compared with LTRE (p = 0.01) and CG (p < 0.0005). In addition, ETRE-PA demonstrated greater vigilance performance compared with LTRE-PA (p = 0.003), LTRE (p < 0.0005), and CG (p < 0.0005) in T1. Both ETRE-PA and LTRE-PA enhanced global cognition compared with LTRE and CG (p < 0.0005) in T1.
For cardiometabolic outcomes, ETRE-PA improved oxygen saturation compared with LTRE (p = 0.005) and CG (p = 0.03). Resting heart rate was reduced in both ETRE-PA and LTRE-PA compared with LTRE (p = 0.009 and p = 0.03, respectively).
Combining ETRE with PA produced greater improvements in eating behavior, cognitive function, oxygen saturation, and cardiometabolic health than LTRE-PA, LTRE, or CG. These findings highlight the importance of aligning dietary timing with exercise to optimize health outcomes in women living with excess body weight.
{"title":"The combination of physical activity and late-time-restricted eating improves eating behavior, cognitive performance and cardiovascular parameters in women living with excess body weight","authors":"Sarra Miladi , Omar Hammouda , Samar J. Miladi Trabelsi , Sirine C. Miladi , Ranya Ameur , Tarak Driss","doi":"10.1016/j.physbeh.2025.115200","DOIUrl":"10.1016/j.physbeh.2025.115200","url":null,"abstract":"<div><div>To evaluate the combined effect of physical activity (PA) and time-restricted eating (TRE) at different times of day (early (ETRE) versus late (LTRE) TRE) on eating behavior, cognitive performance, and cardiovascular parameters in women living with overweight or obesity.</div><div>Sixty one women were randomized into four groups: ETRE combined with PA (ETRE-PA, <em>n</em> = 15, 31.8 ± 10.76 years, 89.68 ± 13.40 kg, 33.5 ± 5.53 kg/m²), LTRE combined with PA (LTRE-PA, <em>n</em> = 15, 30.60 ± 7.94 years, 94.45 ± 15.36 kg, 34.37 ± 7.09 kg/m²), LTRE alone (LTRE, <em>n</em> = 15, 27.93 ± 9.79 years, 88.32 ± 10.36 kg, 32.71 ± 5.15 kg/m²) and a control group (CG, <em>n</em> = 16, 36.25 ± 11.52 years, 89.01 ± 11.68 kg, 33.66 ± 6.18 kg/m²).</div><div>In the post-intervention assessment (T1), ETRE-PA showed a significant reduction in eating disorder global scores compared with LTRE (<em>p</em> = 0.01) and CG (<em>p</em> < 0.0005). In addition, ETRE-PA demonstrated greater vigilance performance compared with LTRE-PA (<em>p</em> = 0.003), LTRE (<em>p</em> < 0.0005), and CG (<em>p</em> < 0.0005) in T1. Both ETRE-PA and LTRE-PA enhanced global cognition compared with LTRE and CG (<em>p</em> < 0.0005) in T1.</div><div>For cardiometabolic outcomes, ETRE-PA improved oxygen saturation compared with LTRE (<em>p</em> = 0.005) and CG (<em>p</em> = 0.03). Resting heart rate was reduced in both ETRE-PA and LTRE-PA compared with LTRE (<em>p</em> = 0.009 and <em>p</em> = 0.03, respectively).</div><div>Combining ETRE with PA produced greater improvements in eating behavior, cognitive function, oxygen saturation, and cardiometabolic health than LTRE-PA, LTRE, or CG. These findings highlight the importance of aligning dietary timing with exercise to optimize health outcomes in women living with excess body weight.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"306 ","pages":"Article 115200"},"PeriodicalIF":2.5,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145743912","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chronic sleep deprivation (CSD), particularly during pregnancy, profoundly impacts maternal and offspring health, driving cognitive, emotional, and physiological disturbances across generations. This review explores the behavioral, neurobiological, and epigenetic consequences of maternal sleep deprivation (MSD), highlighting its mechanisms and transgenerational effects. SD disrupts maternal hormonal balance, elevates stress responses, and compromises neurogenesis, leading to altered maternal behaviors and poor offspring outcomes. Epigenetic mechanisms, including DNA methylation and histone modifications, mediate the transference of SD effects, amplifying risks of anxiety, depression, and cognitive deficits in offspring. These changes impair hippocampal plasticity and immune regulation, exacerbating neuroinflammation and hypothalamic-pituitary-adrenal (HPA) axis dysregulation. Male offspring show heightened sensitivity to metabolic and neurodevelopmental disruptions, indicating a gender-specific vulnerability. Therapeutic strategies such as melatonin supplementation, enriched environments, and nonpharmacological interventions like cognitive-behavioral therapy (CBT) demonstrate potential in mitigating these effects. Promoting maternal sleep hygiene and addressing socioeconomic disparities further protect against adverse outcomes. Emerging evidence underscores the importance of maternal health and lifestyle, emphasizing the need for targeted interventions during pregnancy. Future research should prioritize longitudinal studies to elucidate the mechanisms linking maternal SD to offspring neurodevelopment, evaluate preventive strategies, and address existing gaps in understanding transgenerational epigenetic inheritance. Enhancing maternal well-being through integrated care approaches is essential to improving long-term health outcomes for mothers and their children.
{"title":"Transgenerational effects of sleep deprivation: Behavioral and epigenetic implications for maternal and offspring health","authors":"Harsha Satyapal , Nitu Wankhede , Akanksha Yadav , Sandip Rahangdale , Manish Aglawe , Brijesh Taksande , Samhith Koppula , Milind Umekar , Mayur Kale","doi":"10.1016/j.physbeh.2025.115199","DOIUrl":"10.1016/j.physbeh.2025.115199","url":null,"abstract":"<div><div>Chronic sleep deprivation (CSD), particularly during pregnancy, profoundly impacts maternal and offspring health, driving cognitive, emotional, and physiological disturbances across generations. This review explores the behavioral, neurobiological, and epigenetic consequences of maternal sleep deprivation (MSD), highlighting its mechanisms and transgenerational effects. SD disrupts maternal hormonal balance, elevates stress responses, and compromises neurogenesis, leading to altered maternal behaviors and poor offspring outcomes. Epigenetic mechanisms, including DNA methylation and histone modifications, mediate the transference of SD effects, amplifying risks of anxiety, depression, and cognitive deficits in offspring. These changes impair hippocampal plasticity and immune regulation, exacerbating neuroinflammation and hypothalamic-pituitary-adrenal (HPA) axis dysregulation. Male offspring show heightened sensitivity to metabolic and neurodevelopmental disruptions, indicating a gender-specific vulnerability. Therapeutic strategies such as melatonin supplementation, enriched environments, and nonpharmacological interventions like cognitive-behavioral therapy (CBT) demonstrate potential in mitigating these effects. Promoting maternal sleep hygiene and addressing socioeconomic disparities further protect against adverse outcomes. Emerging evidence underscores the importance of maternal health and lifestyle, emphasizing the need for targeted interventions during pregnancy. Future research should prioritize longitudinal studies to elucidate the mechanisms linking maternal SD to offspring neurodevelopment, evaluate preventive strategies, and address existing gaps in understanding transgenerational epigenetic inheritance. Enhancing maternal well-being through integrated care approaches is essential to improving long-term health outcomes for mothers and their children.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"305 ","pages":"Article 115199"},"PeriodicalIF":2.5,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145687851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Recent studies have found that aerobic exercise improves sensorimotor adaptation. For instance, adaptation to an abruptly-presented 45° visuomotor rotation is improved if preceded by an acute bout of exercise. Still, it is known that adaptation is driven both by an explicit (cognitive) process as well as an implicit process. Given that exercise is known to benefit cognitive function, it remains an open question whether exercise selectively improves implicit adaptation. Here we tested this hypothesis, using a paradigm known to isolate implicit adaptation. In a within-participant design, participants (n = 26) had to reach toward a target, while being pseudo randomly exposed to CW or CCW 30° visuomotor rotations. Implicit adaptation was assessed by the involuntary bias in hand direction that follows a rotated trial, called post rotation bias (PRB). On separate days, participants performed 180 trials before (PRE) and after (POST) a period of exercise, or a period of rest. The exercise bout consisted of 20 min of moderate intensity cycling, which has previously been shown to benefit performance in cognitive and adaptation tasks. Results revealed robust PRBs in both conditions and phases, but critically there was an interaction: the magnitude of PRBs was significantly attenuated following rest, but not following exercise. Further analyses revealed that movements were produced significantly faster following exercise, confirming that exercise impacted motor vigor. By showing that an acute bout of exercise prevents the attenuation of implicit adaptation that is observed following rest, these results indirectly suggest that exercise has a positive effect on implicit adaptation.
{"title":"The effect of an acute bout of exercise on implicit sensorimotor adaptation","authors":"Zivar Beyraghi , Ludovic Arsenault-Lévesque , Jordan Desrosiers , Jean-François Lepage , Pierre-Michel Bernier","doi":"10.1016/j.physbeh.2025.115192","DOIUrl":"10.1016/j.physbeh.2025.115192","url":null,"abstract":"<div><div>Recent studies have found that aerobic exercise improves sensorimotor adaptation. For instance, adaptation to an abruptly-presented 45° visuomotor rotation is improved if preceded by an acute bout of exercise. Still, it is known that adaptation is driven both by an explicit (cognitive) process as well as an implicit process. Given that exercise is known to benefit cognitive function, it remains an open question whether exercise selectively improves implicit adaptation. Here we tested this hypothesis, using a paradigm known to isolate implicit adaptation. In a within-participant design, participants (<em>n</em> = 26) had to reach toward a target, while being pseudo randomly exposed to CW or CCW 30° visuomotor rotations. Implicit adaptation was assessed by the involuntary bias in hand direction that follows a rotated trial, called post rotation bias (PRB). On separate days, participants performed 180 trials before (PRE) and after (POST) a period of exercise, or a period of rest. The exercise bout consisted of 20 min of moderate intensity cycling, which has previously been shown to benefit performance in cognitive and adaptation tasks. Results revealed robust PRBs in both conditions and phases, but critically there was an interaction: the magnitude of PRBs was significantly attenuated following rest, but not following exercise. Further analyses revealed that movements were produced significantly faster following exercise, confirming that exercise impacted motor vigor. By showing that an acute bout of exercise prevents the attenuation of implicit adaptation that is observed following rest, these results indirectly suggest that exercise has a positive effect on implicit adaptation.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"305 ","pages":"Article 115192"},"PeriodicalIF":2.5,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145654830","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-29DOI: 10.1016/j.physbeh.2025.115190
Deyu Meng , Shichun He , Meiqi Wei , Zongnan Lv , Guang Yang , Ziheng Wang
Introduction:
Gut microbiota has been implicated in influencing various health-related behaviors, including physical activity. This study aimed to investigate the causal relationship between gut microbiota and physical activity in individuals of European ancestry.
Materials and Methods:
We conducted a two-sample Mendelian randomization analysis using genome-wide association data from the MiBioGen consortium and the UK Biobank. Numerous gut microbiome taxa were assessed for their causal effect on physical activity measures, including moderate-to-vigorous physical activity, vigorous physical activity, accelerometer-based average acceleration, and higher acceleration levels. Sensitivity analyses evaluated heterogeneity, pleiotropy, and potential reverse causation.
Results:
The analysis identified significant causal links between specific gut microbiome genera and physical activity levels. Key taxa were associated with physiological conditions conducive to exercise and behavior related to physical exertion. Sensitivity analyses confirmed the robustness of these findings, with minimal evidence of heterogeneity or pleiotropy, and reverse causality was largely excluded.
Conclusion:
Gut microbiota may play a causal role in influencing physical activity levels, offering potential for microbiome-targeted interventions to promote physical health.
{"title":"Gut microbiota’s causal effect on physical activity: Insights from two-sample Mendelian randomization analysis","authors":"Deyu Meng , Shichun He , Meiqi Wei , Zongnan Lv , Guang Yang , Ziheng Wang","doi":"10.1016/j.physbeh.2025.115190","DOIUrl":"10.1016/j.physbeh.2025.115190","url":null,"abstract":"<div><h3>Introduction:</h3><div>Gut microbiota has been implicated in influencing various health-related behaviors, including physical activity. This study aimed to investigate the causal relationship between gut microbiota and physical activity in individuals of European ancestry.</div></div><div><h3>Materials and Methods:</h3><div>We conducted a two-sample Mendelian randomization analysis using genome-wide association data from the MiBioGen consortium and the UK Biobank. Numerous gut microbiome taxa were assessed for their causal effect on physical activity measures, including moderate-to-vigorous physical activity, vigorous physical activity, accelerometer-based average acceleration, and higher acceleration levels. Sensitivity analyses evaluated heterogeneity, pleiotropy, and potential reverse causation.</div></div><div><h3>Results:</h3><div>The analysis identified significant causal links between specific gut microbiome genera and physical activity levels. Key taxa were associated with physiological conditions conducive to exercise and behavior related to physical exertion. Sensitivity analyses confirmed the robustness of these findings, with minimal evidence of heterogeneity or pleiotropy, and reverse causality was largely excluded.</div></div><div><h3>Conclusion:</h3><div>Gut microbiota may play a causal role in influencing physical activity levels, offering potential for microbiome-targeted interventions to promote physical health.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"305 ","pages":"Article 115190"},"PeriodicalIF":2.5,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145654502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-28DOI: 10.1016/j.physbeh.2025.115191
Daniela Baptista-de-Souza , Melissa Késsia Cavalcante Oliveira , Ana Claudia Braga-Dias , Silvia Jimena Cardenas Otero , Natália Urel Carneiro , Julian Humberto Avalo-Zuluaga , Lucas Canto-de-Souza , Carlos C. Crestani , Ricardo Luiz Nunes-de-Souza
Chronic pain profoundly impacts mental health, and the social environment significantly modulates pain perception and emotional states. Recognizing the influence of biological sex on pain modulation, basic pain research increasingly investigates sex differences. The hyperalgesic priming protocol effectively models the neuroplastic mechanisms underlying the transition from acute to chronic pain in male and female rodents. Furthermore, accumulating evidence implicates specific hormones, including oxytocin, vasopressin, and corticosterone, in the pathophysiology of pain. This study aimed to determine the interactive influence of sex and social isolation on pain-related behaviors and plasma levels of oxytocin, vasopressin, and corticosterone in mice subjected to hyperalgesic priming. Two experiments were conducted using adult male and female mice (60–63 postnatal days). Experiment 1 assessed mechanical hypersensitivity, facial expression, and anxiety- and depression-like behaviors. In Experiment 2, following a period of social isolation, mice were euthanized, and blood samples were collected via cardiac puncture for plasma hormone analysis. Our results revealed that social isolation impaired recovery from mechanical hypersensitivity and increased facial expressions of pain, specifically in female mice. Independent of sex and hyperalgesic priming, isolation produced heightened anxiety- and depression-like behaviors. Hormonal analyses demonstrated sex-specific effects of isolation. Plasma oxytocin levels decreased upon isolation in both male and female mice. Curiously, primed isolated males showed a recovery of oxytocin levels similar to naïve mice, whereas primed isolated females maintained significantly lower oxytocin levels. Social isolation, coupled with hyperalgesic priming, also decreased vasopressin levels in females. While males displayed higher baseline vasopressin levels, isolation and/or hyperalgesic priming led to a reduction in their plasma vasopressin compared to naïve groups. Curiously, social isolation decreased of corticosterone levels in both males and females. In conclusion, our findings demonstrate that social isolation differentially modulates behavioral and hormonal responses to hyperalgesic priming in a sex-dependent manner, highlighting the complex interplay between social environment, sex, and pain chronification.
{"title":"The interplay of social isolation, sex, and hyperalgesic priming on behavior and hormone levels in a mouse model","authors":"Daniela Baptista-de-Souza , Melissa Késsia Cavalcante Oliveira , Ana Claudia Braga-Dias , Silvia Jimena Cardenas Otero , Natália Urel Carneiro , Julian Humberto Avalo-Zuluaga , Lucas Canto-de-Souza , Carlos C. Crestani , Ricardo Luiz Nunes-de-Souza","doi":"10.1016/j.physbeh.2025.115191","DOIUrl":"10.1016/j.physbeh.2025.115191","url":null,"abstract":"<div><div>Chronic pain profoundly impacts mental health, and the social environment significantly modulates pain perception and emotional states. Recognizing the influence of biological sex on pain modulation, basic pain research increasingly investigates sex differences. The hyperalgesic priming protocol effectively models the neuroplastic mechanisms underlying the transition from acute to chronic pain in male and female rodents. Furthermore, accumulating evidence implicates specific hormones, including oxytocin, vasopressin, and corticosterone, in the pathophysiology of pain. This study aimed to determine the interactive influence of sex and social isolation on pain-related behaviors and plasma levels of oxytocin, vasopressin, and corticosterone in mice subjected to hyperalgesic priming. Two experiments were conducted using adult male and female mice (60–63 postnatal days). Experiment 1 assessed mechanical hypersensitivity, facial expression, and anxiety- and depression-like behaviors. In Experiment 2, following a period of social isolation, mice were euthanized, and blood samples were collected via cardiac puncture for plasma hormone analysis. Our results revealed that social isolation impaired recovery from mechanical hypersensitivity and increased facial expressions of pain, specifically in female mice. Independent of sex and hyperalgesic priming, isolation produced heightened anxiety- and depression-like behaviors. Hormonal analyses demonstrated sex-specific effects of isolation. Plasma oxytocin levels decreased upon isolation in both male and female mice. Curiously, primed isolated males showed a recovery of oxytocin levels similar to naïve mice, whereas primed isolated females maintained significantly lower oxytocin levels. Social isolation, coupled with hyperalgesic priming, also decreased vasopressin levels in females. While males displayed higher baseline vasopressin levels, isolation and/or hyperalgesic priming led to a reduction in their plasma vasopressin compared to naïve groups. Curiously, social isolation decreased of corticosterone levels in both males and females. In conclusion, our findings demonstrate that social isolation differentially modulates behavioral and hormonal responses to hyperalgesic priming in a sex-dependent manner, highlighting the complex interplay between social environment, sex, and pain chronification.</div></div>","PeriodicalId":20201,"journal":{"name":"Physiology & Behavior","volume":"305 ","pages":"Article 115191"},"PeriodicalIF":2.5,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145649113","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}