ライフサイエンスコーパス: feeding behavior

1 directly controls the movements involved in feeding behavior.

2 ptor expressing neurons had no effect on the feeding behavior.

3 granule interneuron production depending on feeding behavior.

4 of diet provides more nuanced insights into feeding behavior.

5 regulating higher-order cognitive aspects of feeding behavior.

6 BA) neurons in mice to compare their role in feeding behavior.

7 t and evidence for their role in controlling feeding behavior.

8 ialist birds known for their touch-dependent feeding behavior.

9 n influence distinct components of motivated feeding behavior.

10 he hypothalamus are critical for homeostatic feeding behavior.

11 pallial amygdala that has been implicated in feeding behavior.

12 elate to its loss of a radula and its unique feeding behavior.

13 g between tanycytes and AN neurons, altering feeding behavior.

14 uate their effects on sucrose perception and feeding behavior.

15 regional heterogeneity in frontal control of feeding behavior.

16 eptides, is a crucial process that regulates feeding behavior.

17 e maintenance of cellular representations of feeding behavior.

18 important molecular mechanism that regulates feeding behavior.

19 that integrates nutrient signals to control feeding behavior.

20 cally modulate ARC(AgRP) neuron activity and feeding behavior.

21 s cell cluster that suppress mating, but not feeding behavior.

22 re both necessary and sufficient for driving feeding behavior.

23 organ, regulating digestion, metabolism, and feeding behavior.

24 gans integrate internal and external cues in feeding behavior.

25 hypothalamus as mediating rapid control over feeding behavior.

26 ention and reward processing and may promote feeding behavior.

27 mic Agrp neurons are known to be crucial for feeding behavior.

28 retory cells and could control locomotor and feeding behavior.

29 ed energy expenditure without alterations in feeding behavior.

30 extrusion in controlling MC4R signaling and feeding behavior.

31 othalamic populations that are important for feeding behavior.

32 hypothalamus to the midbrain responsible for feeding behavior.

33 sting hypotheses about craniodental form and feeding behavior.

34 c inflammation and subsequent alterations in feeding behavior.

35 cilia on hypothalamic neurons in regulating feeding behavior.

36 affects learned and motivational aspects of feeding behavior.

37 controlling synaptic plasticity, memory, and feeding behavior.

38 with both microbiome composition and insect feeding behavior.

39 re part of an extended circuit that mediates feeding behavior.

40 in myc234 drastically modified S. littoralis feeding behavior.

41 cuate nucleus (ARH), a center that regulates feeding behavior.

42 way and neuropeptidergic circuitry governing feeding behavior.

43 omponent of the neural circuitry controlling feeding behavior.

44 the PVT itself may be involved in mediating feeding behavior.

45 pocyte to the central nervous system to time feeding behavior.

46 development of neural circuits that regulate feeding behavior.

47 ical manipulation of opioid receptors alters feeding behavior.

48 ressed in the hypothalamus where it controls feeding behavior.

49 rcuits that are critical for leptin-mediated feeding behavior.

50 rlipidemic rats without affecting the normal feeding behavior.

51 ate the state of satiety into alterations in feeding behavior.

52 hat vector infection by a plant virus alters feeding behavior.

53 e brain sites controlling multiple levels of feeding behavior.

54 naling mediated by the myokine Dpp regulates feeding behavior.

55 unique insight into the executive control of feeding behavior.

56 ase of neuropeptide F (NPF), which regulates feeding behavior.

57 d phospholipid species, some of which affect feeding behavior.

58 the long-lasting effects of AgRP neurons on feeding behavior.

59 ty are not the primary factor driving larval feeding behavior.

60 > septal higher-order circuit that regulates feeding behavior.

61 tide Y (NPY) circuitry is a key regulator of feeding behavior.

62 e modulation of flight performance and blood-feeding behavior.

63 importance in the higher-order regulation of feeding behavior.

64 al basis for an interplay between stress and feeding behaviors.

65 ysical activity, parenting style, and parent feeding behaviors.

66 uces body weight, food intake, and motivated feeding behaviors.

67 isms of the LHA that contribute to motivated feeding behaviors.

68 xtracellular ATP signaling in the control of feeding behaviors.

69 chicken taste buds in association with their feeding behaviors.

70 ies with sediment-associated food chains and feeding behaviors.

71 rate a causal link between cue responses and feeding behaviors.

72 ists of GPR103 could play a role in managing feeding behaviors.

73 th well defined roles in producing different feeding behaviors.

74 ls play critical roles in food selection and feeding behaviors.

75 nxiety, mood, and drug abuse, in addition to feeding behaviors.

76 vous system, thereby disrupting swimming and feeding behaviors.

77 ircuits may trigger deviations from adaptive feeding behaviors.

78 knockdown of AeOBP22 led to reduced mosquito feeding behaviors.

79 antitative trait locus (QTL) analysis of key feeding behaviors.

80 t be reaching parents and influencing infant feeding behaviors.

81 neuroanatomical basis of the stress-related feeding behaviors.

82 ive pathways supporting swimming, escape and feeding behaviors.

83 rgistically with PVH(MC4R) neurons, controls feeding behaviors.

84 s probably made by these insects' integument-feeding behaviors.

85 fluence of context cues on the expression of feeding behaviors.

86 ons mediate bidirectional control of general feeding behaviors.

87 are involved in compulsive and perseverative feeding behaviors.

88 tivity minutes), parenting style, and parent feeding behaviors.

89 an sometimes exhibit hermaphrodite (XX)-like feeding behavior [1, 2].

90 ird ventricle (3V) affected Siberian hamster feeding behaviors; (2) whether food deprivation (FD) co-

91 of these activity patterns during subsequent feeding behaviors accompanied by decreased food intake.

92 geoning literature focusing on addictive and feeding behaviors across multiple domains and levels of

93 c AgRP and POMC neurons in the regulation of feeding behaviors across multiple timescales.

94 cture was analyzed to identify components of feeding behavior affected by Ex4.

95 intervention successfully modified parental feeding behaviors, affected children's diets positively,

96 examining the effects of leptin repletion on feeding behavior after weight loss.

97 owerful tool to dissect the circuit basis of feeding behavior, allowing the efficient implementation

98 (Carcharhinus amblyrhynchos) occurrence and feeding behavior along a marked gradient of isolation fr

99 nd "chrono-nutrition" play a crucial role in feeding behaviors, along with the quality and quantity o

100 ently from the sea lion but displays similar feeding behavior, also has all three Tas1rs inactivated,

101 sue autonomous clocks occur without rhythmic feeding behavior and are lost in constant darkness.

102 in the central nervous system (CNS) affects feeding behavior and body energy stores, the metabolism

103 aria endemicity reflect, in part, changes in feeding behavior and climate adaptation of mosquito vect

104 l energy balance and adiposity by regulating feeding behavior and energy expenditure, the roles for i

105 mation plays an important role in disrupting feeding behavior and energy homeostasis as well as in th

106 s a stomach hormone normally associated with feeding behavior and energy homeostasis.

107 neuropeptides involved in the regulation of feeding behavior and food intake in all vertebrates.

108 the ARC to the PVN are pivotal for balancing feeding behavior and glucose metabolism, we investigated

109 itive processes contribute to the control of feeding behavior and help organism's survival when they

110 dysregulation in part through modulation of feeding behavior and in the absence of an obesogenic die

111 nd regions that are anatomically relevant to feeding behavior and innervated by the trigeminal gangli

112 ophila brain houses the circuitry underlying feeding behavior and is involved in many other aspects o

113 hways specifically in the OSNs impact larval feeding behavior and its body weight.

114 pecies, however, orexin seemed to not affect feeding behavior and its physiological roles are poorly

115 has focused attention on the role of MC4R in feeding behavior and macronutrient intake.

116 ent did not activate c-Fos expression in key feeding behavior and metabolic centers in ZDF rat brain

117 us from regions overlapping with centers for feeding behavior and metabolic control.

118 e brain and is fundamental in the control of feeding behavior and metabolism [1].

119 t the CCAP peptide is a central regulator of feeding behavior and metabolism in adult flies, and that

120 essing neurons in Drosophila adults regulate feeding behavior and metabolism.

121 gulation of physiological responses, such as feeding behavior and mood, and has been implicated in th

122 t the major fat metabolism pathway regulates feeding behavior and NRs could be the mediators to link

123 lucose sensing is involved in the control of feeding behavior and peripheral glucose homeostasis, and

124 phum padi), by examining aphid life history, feeding behavior and plant physiology and biochemistry.

125 ion, we found that neuronal xbp-1s modulates feeding behavior and reproduction, dependent upon tyrami

126 s a strain that exhibits low levels of binge feeding behavior and suggests that this strain could be

127 uronal circuits in the brain help to control feeding behavior and systemic metabolism in response to

128 erphagic conditions plays important roles in feeding behavior and thermogenesis by modulating neurona

129 pothalamus (DMH) has long been implicated in feeding behavior and thermogenesis.

130 ry to assess shark residency in the pass and feeding behavior and used bioenergetics models to unders

131 ed measures of subjective "automaticity" for feeding behaviors and a brief child food-frequency measu

132 Taste compounds elicit innate feeding behaviors and act as rewards or punishments to e

133 a temporal association between limited child feeding behaviors and risk for HHV-8 infection.

134 Few studies have examined observed maternal feeding behaviors and their potential association with c

135 to identify factors associated with maternal feeding behaviors and to test the hypothesis that more m

136 ell function, adipocyte differentiation, and feeding behavior) and presented chemical screening data

137 components, plant growth patterns and insect feeding behavior) and revealed that leaf amino acid cont

138 ous system sites of direct ghrelin action on feeding behavior, and as inspiration for future studies

139 ng POPs and traits such as habitat affinity, feeding behavior, and body size explained some variation

140 The brain ultimately determines feeding behavior, and here we review the mechanisms by w

141 egrates environmental sensory cues to govern feeding behavior, and that basal forebrain signaling, me

142 r is involved in obesity, energy metabolism, feeding behavior, and viability.

143 ted with changes in parental automaticity of feeding behaviors, and program acceptability was high.

144 Importantly, these effects on feeding behavior are observed in the absence of any meas

145 of child obesity is whether and how parental feeding behaviors are associated with the food intake an

146 Accordingly, neurons that contribute to feeding behaviors are localized to central, peripheral,

147 Environmental cues strongly influence feeding behavior, as they can dramatically induce or dim

148 For all parental feeding behaviors, automaticity increased more in the in

149 dered passive feeding as compared with other feeding behaviors because the whales do not swim forward

150 originate in the nervous system and regulate feeding behavior but also peripheral fat regulation thro

151 are known to regulate energy homeostasis and feeding behavior, but how these circuits are established

152 exposure to palatable foods can drive future feeding behavior by "rewiring" mesolimbic dopamine neuro

153 c nociceptin neurons may act as a gateway to feeding behavior by connecting AgRP neurons to both home

154 matode C. elegans detects crowding to change feeding behavior by coupling pheromone sensing to signal

155 , the origins and early evolution of feather-feeding behaviors by insects are obscure.

156 oreover, they displayed a novel head-lifting feeding behavior characterized by holding the vertical p

157 eus, a brain region known to be important in feeding behaviors, conditioned taste aversion, and alarm

158 ) received training on habit formation for 3 feeding behaviors; control participants (n = 68) were as

159 al nervous system responsible for regulating feeding behavior, coupled with metabolic changes due to

160 Animals change feeding behavior depending on their metabolic status; st

161 oreover, these neurons orchestrate different feeding behaviors depending on the magnitude of the stim

162 Here we show that this feeding behavior depends on fat metabolism mediated by t

163 f increasing the homeostatic drive to eat on feeding behavior during appetite suppressing conditions

164 Hypothalamic functions that affect feeding behavior, endocrine function, and circadian rhyt

165 eural circuits relevant to the regulation of feeding behavior, energy expenditure, and glucose homeos

166 d circuits that underscore the regulation of feeding behavior, energy expenditure, glucose homeostasi

167 Feeding behavior engages multiple somatic and visceral t

168 However, these differences in ecology and feeding behavior failed to explain the differences in to

169 to create a compendium of genes relevant to feeding behavior (FB) and/or body weight (BW) regulation

170 ective post-synaptic partners drive opposing feeding behaviors following activation.

171 ced white sharks from SEFI, disrupting shark feeding behavior for extended periods at this aggregatio

172 rtions of frontostriatal systems may release feeding behaviors from regulatory control, thereby perpe

173 erations in circulating hormones involved in feeding behavior, glucose metabolism, hunger, and appeti

174 use of a poor understanding of how different feeding behaviors impact feeding system design (form-fun

175 control one module of female-specific blood-feeding behavior in a deadly vector of infectious diseas

176 Here, we explore the genetic architecture of feeding behavior in a herbivorous insect that has become

177 Taste memories allow animals to modulate feeding behavior in accordance with past experience and

178 limits several starvation-induced changes in feeding behavior in adult Drosophila, including increase

179 properties of SNc mDA neurons and impact on feeding behavior in adult mice.

180 lenges we searched for compounds that affect feeding behavior in C. elegans and sought to identify th

181 ts diet-induced obesity, fat absorption, and feeding behavior in CB(1) cannabinoid receptor-deficient

182 An automated analysis of feeding behavior in freely moving flies shows that IR60b

183 hat have key roles in modulating satiety and feeding behavior in humans.

184 essential regulators of centrally regulated feeding behavior in invertebrates, the role of this prim

185 This review examines human feeding behavior in light of psychological motivational

186 ocation in space to food availability guides feeding behavior in mammals.

187 Our results suggest that feeding behavior in pea aphids is neither simple nor hig

188 In animals, the brain regulates feeding behavior in response to local energy demands of

189 Here, we examine the modulation of feeding behavior in the fruit fly, Drosophila melanogast

190 As a model, we examine the hovering flower-feeding behavior in the hawkmoth Manduca sexta In the la

191 obesity in the mother may lead to unhealthy feeding behavior in the offspring, correlating with alte

192 tightly linked genes) has a major effect on feeding behavior in the pea aphid.

193 genes and/or pathways controlling anemia and feeding behavior in the trypanotolerant N'Dama, coat col

194 Discovery of such a feeding behavior in this ancient, terrestrial, and omniv

195 to the pPVT was sufficient to elicit robust feeding behavior in well fed mice, inhibition of VLM(CA)

196 To address this question, we examined two feeding behaviors in the marine mollusk Aplysia californ

197 They also exhibit a distinctive feeding behavior, in which the premaxilla is cyclically

198 RYGBP-induced altered feeding behavior, including reduced appetite and changes

199 es play important roles in the regulation of feeding behavior, including relaxin-3 (RLN3), which stim

200 es play important roles in the regulation of feeding behavior, including relaxin-3, which acts via th

201 uninfected males, with the frequency of all feeding behaviors increasing by up to threefold, thus in

202 Electrical monitoring of the GPA feeding behavior indicates that the GPA stylets found si

203 he hypothesis that capacity to modify vector feeding behavior is a conserved trait among plant- and a

204 Feeding behavior is a highly complex process with multip

205 that bitter-compound-mediated inhibition on feeding behavior is alleviated by acids.

206 Feeding behavior is heavily influenced by hippocampal-de

207 Feeding behavior is influenced primarily by two factors:

208 igher-order, cognitive circuitry controlling feeding behavior is largely unexplored.

209 Rather, feeding behavior is modulated by various contextual fact

210 Proper circadian alignment of feeding behavior is necessary to prevent metabolic disea

211 or how these interactions lead to changes in feeding behavior is not well-understood.

212 Feeding behavior is orchestrated by neural circuits prim

213 etite center, the hypothalamus, to stimulate feeding behavior is unknown.

214 role of IC cue-related activity in mediating feeding behaviors is poorly understood.

215 ons could not be explained by differences in feeding behavior, locomotor activity, metabolic energy e

216 The oligogenetic basis of variation in feeding behavior may facilitate host shifts, providing o

217 between signals of homeostasis and motivated feeding behavior may inspire new treatment options for e

218 across levels of BMI and varying aspects of feeding behavior may promote the identification of novel

219 ut innervation in INT-BDNF(-/-) mice altered feeding behavior, meal pattern and microstructural analy

220 Feeding behavior, metabolism and circadian clocks are in

221 e function of these receptors with regard to feeding behavior, metabolism, and memory control is poor

222 factors may carry enduring consequences for feeding behavior, metabolism, and obesity risk.

223 ating changes that influence their activity, feeding behavior, metabolism, egg production and gene ex

224 ds caused by pentatomids is related to their feeding behavior, morphology of mouth parts, and saliva,

225 edonic brain nuclei can lead to pathological feeding behaviors, namely overconsumption of highly pala

226 quences of future ocean acidification on the feeding behavior of a deep-sea echinoid, the sea urchin,

227 The blood-feeding behavior of Anopheles females delivers essential

228 use in chimpanzees [3] and in the vocal and feeding behavior of cetaceans [4, 5].

229 BLM and TRA frameworks are confounded by the feeding behavior of D. magna where the ingestion of AgNP

230 ic manipulation of neurons contingent on the feeding behavior of Drosophila to dissect the impact of

231 Little is known about the feeding behavior of hematophagous insects that require p

232 ecting genus in the Bunyaviridae, alters the feeding behavior of its thrips vector, Frankliniella occ

233 r during phytoplankton blooms and the filter-feeding behavior of the blue mussel.

234 eed consumed per day, but did not affect the feeding behavior of the dominant and subordinate fish.

235 faunivory, provide crucial data to infer the feeding behavior of the first dinosaurs.

236 e-driven changes in leaf metabolomics on the feeding behavior of Trichopulsia ni larvae.

237 The feeding behaviors of extinct cave bears living during Pl

238 This finding demonstrates that feather-feeding behaviors of insects originated at least in mid-

239 This inferred feeding behavior offers a generalized view of dinosaur f

240 ks, and potential impacts of those roles and feeding behavior on associated extinctions.

241 the SCN and the number of influences such as feeding behavior on circadian rhythm.

242 ranscript by RNA interference disturbs aphid feeding behavior on fava beans measured by the electrica

243 is whether to engage in active movement and feeding behavior or to become quiescent.

244 at regulate insulin-like peptide expression, feeding behavior, or both.

245 ing meal frequency, daytime versus nighttime feeding behavior, or locomotor activity.

246 agal afferents are involved in regulation of feeding behavior, particularly meal size, and have been

247 ation for the onset of peak circadian insect feeding behavior, providing evidence for the underlying

248 ion in single flies and assess the impact on feeding behavior quantitatively and with high throughput

249 ersatile regulator of energy expenditure and feeding behavior, rapidly binds neurons in the vicinity

250 Feeding behavior rarely occurs in direct response to met

251 ccount for the previously reported decreased feeding behavior, reduced growth rates and aborted devel

252 MCT1 expression in tanycytes plays a role in feeding behavior regulation.

253 r perceived food quality into alterations in feeding behavior remains poorly understood.

254 Feeding behaviors require intricately coordinated activa

255 n (POMC) positively and negatively influence feeding behavior, respectively, possibly by reciprocally

256 tal modulation of two distinct components of feeding behavior: reward valuation based upon taste perc

257 BMI and feeding-behavior scales were transformed to SD scores.

258 thesis is that the transition to maladaptive feeding behavior seen in eating disorders or obesity may

259 ion promoting habit formation for 3 parental feeding behaviors: serving fruit/vegetables, serving hea

260 This work suggests that feeding behaviors should be an intrinsic part of future

261 eras), permit in situ observations of shrimp feeding behavior, shrimp size and internal anatomy, and

262 ominantly anchovies, demonstrated a range of feeding behaviors such as oblique, vertical, and lateral

263 erences in a number of phenotypes, including feeding behavior, such as filter feeding in the Mysticet

264 ulate energy stores, free glucose levels, or feeding behavior suggesting the sleep phenotype of trsn

265 neurons disrupts conditioned, but not naive, feeding behavior, suggesting these neurons are selective

266 halamus (LH) has long been known to regulate feeding behavior, taste processing in LH remains relativ

267 mbionts (i.e. yeast-like symbionts, YLS) and feeding behavior that can interact to affect the spread

268 e loopers (Trichoplusia ni) display rhythmic feeding behavior that is sustained under constant condit

269 restriction leads to an altered anticipatory feeding behavior that temporarily abrogates the anorecti

270 sary and sufficient to stimulate a reflexive feeding behavior, the proboscis extension reflex (PER),

271 here it can increase motivational aspects of feeding behavior through effects on dopamine output in t

272 rons and motoneurons, and, in one case, link feeding behavior to gut peristalsis and locomotion.

273 r and NRs could be the mediators to link the feeding behavior to the metabolic changes.

274 ircuitry linking the brain areas involved in feeding behavior to the olfactory regions is not well kn

275 fts or sleep deprivation, it markedly alters feeding behaviors ultimately promoting obesity and insul

276 ulation of the NPY/AgRP neurons that promote feeding behavior until satiety signals kick in.

277 of color vision on reproductive success and feeding behavior using nine years of morphological, demo

278 arning algorithm lasso to predict aspects of feeding behavior using VS LFPs.

279 h suggests that colon-derived SCFAs modulate feeding behavior via central mechanisms.

280 teral hypothalamus (LHA) regulates motivated feeding behavior via GABAergic LHA neurons.

281 ehaviors from more than 1400 observations of feeding behaviors video-recorded in a wild population of

282 rvation and participate in the expression of feeding behavior was comparable in OEA-treated WT and HD

283 sterase (PME) activity on aphid settling and feeding behavior was evaluated by free choice assays and

284 This suspected feeding behavior was less appreciable in the presence of

285 ing electrophysiological monitoring of aphid feeding behavior, we demonstrate that Mp708 provides phl

286 In classifying feeding behavior, we found an optimal balance between mo

287 Neuropeptide expression and feeding behavior were measured in MCT1-inhibited animals

288 dy distribution, and (iii) effect on isopods feeding behavior were observed regardless of whether the

289 experimental enclosure where observations of feeding behavior were performed.

290 Aphid feeding behaviors were negatively impacted on NAM spraye

291 et a background motivational tone regulating feeding behavior, whereas beta-endorphin underlies orose

292 Activation of TPNs influences innate feeding behavior, whereas inhibition has little effect,

293 pseudogenized, consistent with their unique feeding behavior, which entails swallowing food whole wi

294 Functionally, the PSTN is involved in gating feeding behavior, which is conceptually homologous to th

295 NPF acutely increases sleep without altering feeding behavior, which it affects only on a much longer

296 imals show decreased body weight and altered feeding behavior with reduced food and water intake.

297 These included reduced blood feeding behavior, with almost 100% of insects infected w

298 nal nutrient sensors play important roles in feeding behavior, yet their molecular structure and mech

299 and nutrient additions influenced herbivore feeding behavior, yet while sea urchins preferred nutrie

300 an enteric serotonergic neuron, and adaptive feeding behaviors, yielding a new view of how enteric ne