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1 fraction alters body weight and behavioural despair.
2 munity- and state-level solutions to address despair.
3 oes not ask what protects those nations from despair.
4 ely contributed to the rise in the deaths of despair.
5 and protecting individuals and families from despair.
6 l in responding to the epidemic of deaths of despair.
7 h (R,S)-ketamine and FENM reduced behavioral despair.
8 aveling through times of both excitement and despair.
9 not be explained by anhedonia or behavioral despair.
10 ation facilitated depression-like behavioral despair.
11 MDA receptor antagonist, reversed behavioral despair.
12 viduals either show resilience or succumb to despair.
13 ly correlated with the extent of behavioural despair.
14 elicited anhedonia and increased anxiety and despair.
15 feeding behaviour, anhedonia and behavioural despair.
16 emselves at the crossroads of prosperity and despair.
17 arch toward clinically useful definitions of despair.
18 fear and decreased stress-induced behavioral despair.
19 te populations) had higher RRs for deaths of despair.
20 duction in reward responsivity and increased despair.
23 , leaving some anxiety (if not confusion and despair) about molecular monitoring in the day-to-day tr
24 y, increased aversive memory, and behavioral despair, acting at the medulla, prefrontal cortex, and a
27 r 2000 or 2010 had higher rates of deaths of despair and all-cause midlife mortality at baseline but
28 pathway is critical for mediating behavioral despair and antidepressant-like responses to leptin.
30 d psychological distress (PD) as a proxy for despair and drew data from the US National Health Interv
31 onomic insecurity and increases in deaths of despair and midlife all-cause mortality in US counties d
35 al areas with high prevalence of diseases of despair, and 1 focus group with 17 members in a high-pre
36 sufficient to cause helplessness, behavioral despair, and anxiety-like behavior in mice, establishing
40 sponse to acute stress, increased behavioral despair, and no behavioral response to antidepressant, m
42 venile or adult windows, increased anxiety-, despair-, and schizophrenia-like behavior in adulthood.
43 tivation, together with increased behavioral despair, anhedonia, and anxiety-related behavior in the
45 le mortality (SDAM)-often labeled "deaths of despair"-are increasing among working-aged individuals i
46 not increases in measurements of behavioural despair, are prevented by blocking these melanocortin 4
49 In direct measures of their resistance to despair behavior, TASK-3 knock-outs displayed significan
51 o discrete categories of "reward behavior," "despair behavior," "anxiety-like behavior," and "cogniti
55 RP neurons completely reverses anhedonic and despair behaviors induced by chronic unpredictable stres
59 , a commonly used animal model of behavioral despair/depression, leads to an increase in central or p
61 allel increases in corresponding diseases of despair (DoD), indicating that there could be an associa
62 unpredictable stress and improved behavioral despair dose-dependently in the forced swim test (FST),
63 th needs may improve processes to screen for despair (eg, social history taking) and codesign primary
64 underestimated the mortality consequence of despair for Whites and Blacks but overestimated it for H
66 ontribute more meaningfully to the deaths of despair framework (i.e., conceptualizing rises in suicid
67 Research) database on county-level deaths of despair from 2000 to 2019 across racial and ethnic group
68 e but similar rates of increase in deaths of despair from 2001 to 2015 compared with counties with st
70 d common factors associated with diseases of despair, highlighting the association between long-term
71 e decline focused on increases in "deaths of despair" (i.e., deaths from suicide, drug use, and alcoh
75 ike effect of leptin in reversing behavioral despair in both the tail suspension and forced swim test
76 We observed similar resistance to behavioral despair in distinct mutant mice lacking HCN1 or HCN2.
77 ime and saccharin preference, and behavioral despair in female mice and enhanced stress-induced decre
78 ufficient to induce anhedonia and behavioral despair in males but not females under non-stress condit
81 isparities in infant mortality and deaths of despair in the 19 US CDs of Pennsylvania for the 111th-1
82 nt after acute stress, increased behavioural despair in the forced swim test, and decreased sucrose p
85 ncreasing midlife death rates and "deaths of despair," including suicide, chronic liver disease, and
86 ear extinction deficit, increased behavioral despair, increased anxiety-related behaviors in the ligh
91 via 2 distinct Hb circuits, contributing to despair-like behavior (Hb-MOR/interpeduncular nucleus) a
92 ons - negative processing biases, anhedonia, despair-like behavior (learned helplessness) - affords u
94 the forebrain of mice induces alterations in despair-like behavior and HPA axis function, reminiscent
95 8) treatment with the impact on anxiety- and despair-like behavior examined in adulthood, along with
99 ng-lasting, opposing changes in anxiety- and despair-like behavior in male, but not female, rats.
100 mobile (WMI) substrain shows high immobility/despair-like behavior in the forced swim test (FST), whi
103 evoked increase and decrease in anxiety- and despair-like behavior, respectively, were accompanied by
105 creased social deficit, anxiety-related, and despair-like behaviors during protracted forced abstinen
108 ior in the Elevated Plus Maze and behavioral despair-like immobility in the Forced Swim Test are cont
110 ar nucleus terminals triggered avoidance and despair-like responses with no anxiety-related effect, w
111 rced swim test (FST) which was indicative of despair-like state, and loss of taste preference in sacc
112 l effects of SSRIs in the chronic behavioral despair model of depression both in the presence and in
113 tated in animals subjected to the behavioral despair model, which was prevented by SSRI treatment.
115 ic advancement in deciphering the "deaths of despair" narrative, most relevant studies have focused o
116 mpathized with the initial hope and ultimate despair of potential recipients who must continue their
117 ity and lower social mobility with deaths of despair on both the additive and multiplicative scales f
119 the antidepressant fluoxetine in behavioral despair paradigms, whereas fluoxetine normalizes their a
120 s but overestimated it for Hispanics; and 2) despair partially contributed to the DAS trend among Whi
122 spect to awareness and believed causation of despair-related illness, and participants identified com
124 sociated with additional risks for deaths of despair, suggesting that addressing the underlying socia
125 he rise is largely attributable to deaths of despair (suicide and poisoning by alcohol and drugs) wit
127 loskeletal, cardiorespiratory, distress, and despair symptoms at baseline and increases during the fo
129 nt-like effect in the forced swim behavioral despair test, and this effect was blocked by ablation of
131 that precede these -often denoted-"deaths of despair." This paper examines whether a childhood interv
133 around 2 themes: (1) building resilience to despair through better community and organizational coor
135 tion between religiosity and the diseases of despair via regression, sibling fixed effects (SFE) anal
137 buted to the dramatic rise in the "deaths of despair." We contribute to the recent epidemiologic lite
138 dy, high-prevalence hotspots for diseases of despair were identified from health insurance claims dat
139 d, 152 350, 149 589, and 1 250 156 deaths of despair were recorded for working-age Hispanic, non-Hisp
140 cedure commonly used for inducing behavioral despair, were simultaneously monitored in real time.
141 d resistance to multiple tasks of behavioral despair with high predictive validity for antidepressant
142 nurses, and researchers today, the depth of despair wrought by the HIV/AIDS epidemic at that time is