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1 fective analgesics, but they are also highly addictive.
2 SCRAs are highly potent and addictive.
10 eflect the burgeoning literature focusing on addictive and feeding behaviors across multiple domains
14 wer pharmacokinetics, which results in fewer addictive and reinforcing effects than cocaine; the effe
15 y those high in refined sugars and fats, are addictive and that some forms of obesity can usefully be
18 erally safe in a clinical setting, it can be addictive, and several of its derivatives are being inve
21 t overeating of palatable food is similar to addictive behavior and characterized by dysregulation of
23 s depressive-like effects and contributes to addictive behavior in male nonhuman primates and rodents
25 defense functions; the partially selfish and addictive behavior of the defense systems; and coupling
26 Substantial evidence from rodent models of addictive behavior points to the involvement of the vent
28 et region amygdala, a key area implicated in addictive behavior, differs depending on the GATA4 genot
29 eural systems interact with sex to influence addictive behavior, emphasizing throughout that the impa
32 ability of neuropsychiatric traits including addictive behavior, schizophrenia, and neuroticism, thus
33 e synaptic changes associated with facets of addictive behavior, supporting partial coincident neurol
34 king behavior, novelty-seeking behavior, and addictive behavior, we hypothesized alterations of the f
35 tly or indirectly-to processes of reward and addictive behavior, with a focus on psychostimulants and
48 -analysis, representing 643 individuals with addictive behaviors and 609 healthy control individuals.
51 mesolimbic dopamine system, suggesting that addictive behaviors are encoded by changes in the reward
53 d aggression, impulsivity, and proclivity to addictive behaviors compared with low-novelty reactive r
55 ibute to impulsivity, which is a hallmark of addictive behaviors that underlie compulsive drug seekin
56 t the applicability of theoretical models of addictive behaviors to the social-networks-use disorder
57 ociated memories is critical for maintaining addictive behaviors, as presentation of drug-associated
58 re central to pain control, drug reward, and addictive behaviors, but underlying circuit mechanisms h
71 ce use or gambling; participants at risk for addictive behaviors; and studies using the same patient
73 ons, including response to oxidative stress, addictive behaviour, and regulatory functions emphasizin
77 on phenotype can be abrogated in the cystine-addictive cells by miR-200c, which converts the mesenchy
79 s in the rate of metabolism of nicotine, the addictive chemical in tobacco, affect smoking behavior a
86 xtracellular transmitter and is a target for addictive compounds such as cocaine, amphetamine (AMPH),
88 ucts are cotinine, a major metabolite of the addictive constituent nicotine, and 4-(methylnitrosamino
98 l intermediate phenotype (endophenotype) for addictive disorders and comorbid externalizing psychopat
101 value in this regard, because both pain and addictive disorders are characterized by impaired hedoni
102 related disorders, and substance-related and addictive disorders as well as in end-of-life care.
103 t state of knowledge of reward processing in addictive disorders from a widely used and validated tas
107 literature on the use of neuromodulation in addictive disorders to highlight progress limitations wi
108 idual HR associated with dispensed drugs for addictive disorders was 0.48 (95% CI, 0.23-0.97), based
109 depressants, psychostimulants, drugs used in addictive disorders, and antiepileptic drugs) after pris
111 ge of the importance of genomic variation in addictive disorders, and provide an addiction CNV pool f
112 disorder, to extend these findings to other addictive disorders, and to relate variations in them to
113 allow us to probe affected brain circuits in addictive disorders, but also seem to have unique therap
114 ntribute to symptoms in eating disorders and addictive disorders, but little is known about the molec
115 ipsychotics, psychostimulants, and drugs for addictive disorders, compared with periods in which they
116 atic symptom disorder, substance-related and addictive disorders, feeding and eating disorders, schiz
117 ariation in addictions, shared mechanisms in addictive disorders, impact of changing environmental in
118 ed across a network of regions implicated in addictive disorders, including insula, superior temporal
119 otivation and have been repeatedly linked to addictive disorders, including nicotine dependence.
120 kappa-opioid receptor (KOR) abnormalities in addictive disorders, other central nervous system diseas
121 in the risk for and clinical presentation of addictive disorders, risk for addiction may be different
122 d dopamine D2 receptor (D2R) availability in addictive disorders, the role that these systems play in
123 s have been linked to impaired cognition and addictive disorders, we hypothesized that reduced GABA i
124 eness is shared across other psychiatric and addictive disorders, we predicted that as rates of smoki
135 fying amphetamine (AMPH), cocaine, and other addictive dopamine-transporter inhibitors (DAT-Is) suppo
136 ction with a peer and then choose between an addictive drug (heroin or methamphetamine) and social in
137 amine, a potent psychostimulant, is a highly addictive drug commonly used by persons living with HIV
139 ol.SIGNIFICANCE STATEMENT Over the course of addictive drug exposure, there is a transition in the co
146 Although cocaine is known to be a highly addictive drug, there appears to be a select subset of i
147 002 to 0.0052; p=0.069), and the presence of addictive-drug metabolites in urine (0.103, -0.013 to 0.
148 By increasing dopamine in the striatum, addictive drugs alter the balance of dopamine and glutam
149 al tegmental area (VTA) is a major target of addictive drugs and receives multiple GABAergic projecti
150 vern activity-dependent synaptic plasticity, addictive drugs can derail the experience-driven neural
151 of the brain mechanisms they activate; most addictive drugs cause elevations in extracellular levels
153 ely used to study motivational properties of addictive drugs in animals, but has rarely been used in
156 red the observation that a common feature of addictive drugs is to activate, by a double tyrosine/thr
158 a (VTA) dopamine (DA) neurons in response to addictive drugs may underlie the transition from casual
159 SIGNIFICANCE STATEMENT: It is believed that addictive drugs often render an addict's brain reward sy
161 ressive predominance of rewarding effects of addictive drugs over their aversive properties likely co
164 tamate interaction in MSN that is usurped by addictive drugs to elicit persistent behavioural alterat
166 Many studies support a perspective that addictive drugs usurp brain circuits used by natural rew
168 nally address the question of whether or not addictive drugs usurp the neuronal networks recruited by
169 ediction of the three most frequently abused addictive drugs with the sensitivity and accuracy of the
171 ral tegmental area (VTA) are a key target of addictive drugs, and neuroplasticity in this region may
174 yle but also the immunomodulatory effects of addictive drugs, such as cocaine, may account for their
175 esolimbic dopamine-a defining feature of all addictive drugs-as a neural substrate for these drug-ada
184 hyperpalatable foods associated with a quasi-addictive effect and that the prevailing European Union
188 se data suggest a possible mechanism for the addictive effects of Delta(9)-tetrahydrocannabinol in ju
189 Neuronal acetylcholine receptors mediate the addictive effects of nicotine and may also be involved i
190 s (MORs) are necessary for the analgesic and addictive effects of opioids such as morphine, but the M
197 limiting adverse effects and are potentially addictive, highlighting the need for improved therapeuti
198 ambling or video-game play may be considered addictive in the absence of exogenous (i.e. drug-induced
201 effects of opioids that may lead to a lower addictive liability of opioids with selective low potenc
202 nsistent with these impairments, we observed addictive-like behavior in DIO-prone rats, including 1)
203 iet-induced obesity (DIO) is associated with addictive-like behavior, as well as synaptic impairments
205 tributes to the transmission of MHFD-induced addictive-like behaviors and obesogenic phenotypes acros
208 ational HFD exposure leads to more prominent addictive-like behaviors with reduced striatal dopamine
209 onfer resilience to poor decision making and addictive-like behaviors, such as excessive ethanol drin
210 zygotes reproduces obesogenic phenotypes and addictive-like behaviors, such as increased preference o
213 is at the center of a variety of cognitive, addictive, mood, anxiety, and developmental disorders.
215 ugh long-term exposure to nicotine is highly addictive, one beneficial consequence of chronic tobacco
217 ch engages numerous components of tumor cell-addictive pathways and highlights the ability to deliver
219 hese results indicate that GRIP may modulate addictive phenotypes through its regulation of synaptic
220 and e-cigarettes contain nicotine, a highly addictive, plant-derived alkaloid that binds to nicotini
222 r pipe smoking, and misperceptions about the addictive potential and potential adverse health effects
224 V on COT, opioid misuse and awareness of the addictive potential of COT are common, yet COT monitorin
225 e may be increasing among youth, however the addictive potential of pregabalin has not been well esta
228 Methamphetamine (METH) is a drug with a high addictive potential that is widely abused across the wor
237 selected clusters are highly relevant to the addictive process, including regions relevant to cogniti
238 te use in humans and highlight the potential addictive properties and harmful effects of chronic nico
246 oward a better understanding of the proposed addictive properties of food, the components and the mec
247 responsible for mediating the analgesic and addictive properties of most clinically relevant opioid
248 e on a habenula-pancreas axis that links the addictive properties of nicotine to its diabetes-promoti
255 nconsistent with its therapeutic effects and addictive properties, which are thought to be reliant on
263 products usually contain nicotine, which is addictive, raising concerns about e-cigarette use and ni
264 t increased G9a expression in NAcSh enhances addictive-related and anxiety-related behaviors, indicat
267 This overactivity may be associated with the addictive scratching and/or neural hypersensitization.
269 have important implications for learning in addictive states marked by elevated direct pathway activ
271 racterization of peptidomic regulation by an addictive substance along two distinct projection system
275 1) increase craving, impatience, and actual addictive substance use and 2) do so through mechanisms
276 with those that influence the rate at which addictive substance use is taken up during adolescence a
278 ., cola, soft drinks, and energy drinks) and addictive substances (nicotine, caffeine, alcohol, canna
280 s at genetic risk for both escalating use of addictive substances and poor abilities to quit may prov
283 atent class that displayed low use of common addictive substances during adolescence (P=0.0004) and (
286 large amounts of sugar also tend to use more addictive substances, but it is unclear whether this is
287 s of drug addiction: high motivation to seek addictive substances, despite adverse consequences, and
288 lity traits, intelligence, happiness, use of addictive substances, parental separation, age, and gend
295 and Validation of Biomarkers to Develop Non-Addictive Therapeutics for Pain workshop convened scient
297 partially effective and in some cases can be addictive, underscoring the need for better therapies.
298 These 2 effects may combine to explain the addictive use of levodopa after loss of midbrain dopamin
299 reating chronic pain, but opioids are highly addictive when repeatedly used because of their strong r