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4 ng premature pruning of dendritic spines and allostatic atrophy of dendritic arborization in early ad
5 he hypothesis that chronic stress induces an allostatic attenuation of the mesolimbic dopaminergic sy
6 ay be explained by a maladaptive feedforward allostatic cascade model and how understanding migraine
7 at moderate intoxicating levels, induces an allostatic change in the brain functional connectivity t
8 l forebrain and cingulate cortex may mediate allostatic changes in sleep time and intensity observed
10 rlying these adaptive, or more specifically, allostatic, changes in sleep homeostasis are unknown.
12 also review how homeostatic, circadian, and allostatic drives help regulate sleep state switching an
13 nged by findings suggesting a domain-general allostatic function for oxytocin by promoting future-ori
17 ording to the reward deficiency syndrome and allostatic hypotheses, hyposensitivity of mesocorticolim
18 theory-driven predictions based on levels of allostatic interoception associated with bvFTD phenomeno
19 a new research agenda for understanding how allostatic interoception involves brain predictive codin
20 ss the biological mechanisms associated with allostatic interoception, including whole-body cascades,
21 ew, we explore the disruptions in integrated allostatic interoceptive mechanisms in psychiatric and n
22 ascades, brain structure and function of the allostatic interoceptive network, heart-brain interactio
23 We synthesize new pathways to understand how allostatic interoceptive processes modulate interactions
28 uggest that bvFTD may be characterized by an allostatic-interoceptive overload manifested in ongoing
30 contribute to the complex associations among allostatic load (a marker of chronic stress), educationa
31 cer death between educational attainment and allostatic load (adjusted for age, income, and smoking s
32 neighborhood risk of psychosocial stress on allostatic load (AL) among adolescents as a mechanism th
33 w studies on human populations have examined allostatic load (AL) as it relates to cancer risk, progr
41 ssociation between residential greenness and allostatic load (AL), a marker of composite physiologica
42 ing biomarkers of stress, including IL-6 and Allostatic Load (AL), can also serve as early indicators
43 consequences of chronic stress, measured by allostatic load (AL), may contribute to these disparitie
44 study is to examine the relationship between allostatic load (AL), neighborhood opportunity, and all-
45 rrelates of adverse SDHs, operationalized as allostatic load (AL), with mortality due to lung cancer.
47 ved that TL had a negative relationship with allostatic load (beta = - .320 p = .017) and a cardiomet
48 With increasing severity and over time, the allostatic load (increase in glycemia) may have patholog
49 , high ADI group had higher median levels of allostatic load (P = 0.046) and lower median levels of g
50 group were 20% more likely to have increased allostatic load and 51% less likely to have increased le
54 men (HR, 5.77; 95% CI, 4.06-8.20) with high allostatic load and less than high school educational at
55 imulated leukocytes would show signs of high allostatic load and low levels of protective psychosocia
57 ssors could provide molecular correlates for allostatic load and predict healthy or maladaptive stres
58 GR gene expression can lead to an increased allostatic load and result in an "aging-like" phenotype
59 ing a high school degree, combined with high allostatic load as a marker of chronic stress, with canc
63 Our findings indicate that mitochondrial allostatic load contributes to BD, suggesting mitochondr
68 was used to assess IL-6 and create composite allostatic load measure including: IL-6, blood pressure,
70 understanding migraine within the context of allostatic load model suggests alternative treatments fo
71 od experience was positively associated with allostatic load of children at 6 y of age at higher leve
73 we then posit the potential implications of allostatic load on patient care and research in cardio-o
75 reflects an allostatic process, and that the allostatic load produced by SD has direct effects on the
78 ect long-term risk associated with increased allostatic load resulting from the stimulation of insuli
81 most deprived quintile had 1.13 times higher allostatic load than those living in the least deprived
82 gins by noting two new terms, allostasis and allostatic load that are intended to supplement and clar
88 the association between cumulative risk and allostatic load was attenuated for adolescents who score
91 ence of multiple risk factors) on children's allostatic load were assessed in 260 children (46% femal
94 d; cross-systemic phenotypes, combined into "allostatic load") and agnostic (DMR-based) pathway enric
96 tics and experiences of societal inequality (allostatic load) increase the complexity of studying bre
97 adaptation results in a physiological cost (allostatic load) that might impair the homeostatic stres
100 ociation between chronic stress exposure and allostatic load, a biological marker of chronic physiolo
102 iation between neighbourhood deprivation and allostatic load, a biological marker of wear and tear, t
104 dults from low-income families manifest more allostatic load, an index of chronic physiological stres
105 could potentially be associated with higher allostatic load, but few studies to date have quantified
106 systemic biological risk (MSBR), a proxy for allostatic load, is a composite index of biomarkers repr
107 ople with type 2 diabetes experience chronic allostatic load, manifest as dynamic disturbances in rea
109 eoretical constructs, such as weathering and allostatic load, regarding the power of chronic environm
110 specific physiological norms, allostasis and allostatic load, stochasticity, and decline in stress re
111 actors and cancer outcomes, including higher allostatic load, stress hormones, altered epigenome and
112 selected markers of biological aging (e.g., allostatic load, telomere length, and global DNA methyla
124 ntext of health; (b) the stress response and allostatic load; (c) some of the key biological mechanis
125 We found that repeated seizures cause an allostatic maladaptation of AEA signaling in the amygdal
128 the existence of organ-specific compensatory allostatic mechanisms are robust enough to drive an unex
129 hat this phenomenon is regulated by cellular allostatic mechanisms that elevate the muscle glycogen s
132 g homologous activation of the interoceptive-allostatic network across primate species during affecti
134 to severe or repeated stressors-can lead to allostatic (over)load, causing wear and tear on tissues,
138 xt of repeated sleep restriction reflects an allostatic process, and that the allostatic load produce
140 n as a motivational incentive because due to allostatic reference resetting, more stimuli are require
144 unrelated to physiological needs induces an allostatic regulatory state that defends a supranormal a
146 ogical stressors are frequent and/or severe, allostatic responses can become dysregulated and maladap
148 or is lost in either neuronal population, an allostatic shift will occur leading to a long-term dysre
149 mical dysregulations that ultimately form an allostatic state (decreased dopamine and opioid peptide
150 er metabolism could contribute to an altered allostatic state and therefore be involved in continued
152 local physical stimulation, cells trigger an allostatic state that maximizes energy and overcomes a m
157 necessary step in the development of complex allostatic systems and suggest that intrinsic and social