ライフサイエンスコーパス: suckling

1 e in burst firing evoked by applied OT or by suckling.

2 in expression and activity were found during suckling.

3 ifferentially regulated by either PRL and/or suckling.

4 espond to neural signals from termination of suckling.

5 nses to cues important for the initiation of suckling.

6 ubjected to greater mechanical stress during suckling.

7 rats in response to any stimulus other than suckling.

8 in only 3% (n = 77) of newborn lambs before suckling.

9 ntrol of the secretion of PRL in response to suckling.

10 C in the outer zone of the AL (AL-OZ) due to suckling.

11 pt capacity to extract energy from milk upon suckling.

12 ause of a progressive rise in their Tb while suckling.

13 ntributed to heat retention in mothers while suckling.

14 orodibenzo-p-dioxin (TCDD), in utero and via suckling.

15 at are learned and recognized prior to first suckling.

16 ethanol was tested in newborn rats naive to suckling (3-5 hr old) on Postnatal Day (P) 0 and in olde

17 t undergo rapid postnatal catch-up growth by suckling a control-fed dam (recuperated offspring).

18 e-Dawley rats were fed, during pregnancy and suckling, a control diet (4% w/w corn oil) or a fatty ac

19 esent study was to determine if any of these suckling activated areas project directly to the DMH.

20 showed marked depression of respiratory and suckling activities in vivo and overexpression of synapt

21 yses indicate that hSRY(ON) pups lack innate suckling activities, and develop fatty liver disease, ar

22 rmal newborn mice mimicked the depression in suckling activity but not respiratory depression in vivo

23 ing and handling as well as of the pups' own suckling activity-but not food intake-fully restored CRF

24 es to regulate social behaviours such as pup suckling, aggression and mating.

25 dA was also induced during infections of the suckling and adult mouse intestines, and in vitro under

26 affected by their growth rate when they were suckling and find that limiting growth during that perio

27 Unilateral inhibition of suckling and hormonal reconstitution experiments showed

28 porin 4 association decreased during initial suckling and increased after the MER, whereas opposite c

29 odulate sensory-motor reflexes necessary for suckling and may be part of the mechanism by which intra

30 has knock-out mice (Gnasxl(m+/p-)) have poor suckling and perinatal lethality, implicating XLalphas a

31 The combination of nonnutritive suckling and sucrose (7.5%, 0.01-0.06 ml/min) infusion m

32 Non-nutritive suckling and warm temperatures blunted this effect.

33 ult distal intestinal microbiota, during the suckling and weaning periods.

34 is up-regulated during embryogenesis, during suckling, and in the mother during pregnancy.

35 strous; control of reproduction, aggression, suckling, and parental behaviors; individual recognition

36 ial role in the digestion of dietary fats in suckling animals.

37 vements in utero to the postnatal mastery of suckling at 4 months after birth; and (2) thereafter, fr

38 was no indication that mothers discontinued suckling because of a progressive rise in their Tb while

39 g imaging sessions, dams were exposed to pup suckling before and after administration of an oxytocin

40 Impaired suckling behavior was attributable to defective olfactio

41 dysmorphism, semilethality due to defective suckling behavior, and generation of a small fraction of

42 th the same amount of water had no effect on suckling behavior.

43 ory conditioning has the potential to modify suckling behavior.

44 with milk may reinforce components of early suckling behavior.

45 ew technique for experimental study of early suckling behavior.

46 also used data on inter-birth intervals and suckling behaviours to determine whether the duration of

47 stnatal physiological adaptations, including suckling, blood glucose and energy homeostasis.

48 quencing and qPCR showed that, compared with suckling, bottle feeding significantly increased the abu

49 Approximately half the pups suckling Btn1a1(-/-) animals died within the first 20 da

50 onsistent with augmented cylindrical growth, suckling but not adult transgenic mice show enlarged cry

51 es after ETEC challenge were associated with suckling but not birthing from vaccinated dams, suggesti

52 developed a severe cachexia during high fat suckling, but caught up in weight after switching to a c

53 f contaminants from the mother cows to their suckling calf and the uptake of soil by grazing cattle.

54 Finally, suckling caused dissociation of OTRs and G beta subunits

55 vements in mammals, e.g., walking, swimming, suckling, chewing, and breathing, inhibition is often hy

56 Changes in brain activation in response to suckling closely matched that elicited by oxytocin admin

57 n the same (CC, OO) or alternate diet during suckling (CO, OC) and weaned onto standard chow.

58 milk formula via artificial rearing, and (3) suckling control (SC), where pups remained with lactatin

59 ties were detected from duodenum to colon in suckling CONV mice, but the relative levels of these act

60 The suckling defect was responsible for the death among lp(A

61 Here we show that Hap1 null mutants display suckling defects and die within the first days after bir

62 s of ALEX is most likely responsible for the suckling defects previously observed.

63 olfactory defect resulting in a competitive suckling deficit.

64 Feeding and suckling deficits in infants with PWS are replaced with

65 in VMH are governed primarily by maternal or suckling-derived sensory input rather than food intake o

66 The timing of the last week of suckling did not differ by infant body mass.

67 These results indicate that suckling elicits dynamic glial neuronal interactions in

68 including opioid activity, during the first suckling episode.

69 the first demonstration that OT mediation of suckling-evoked bursts/milk ejections is via interaction

70 e injected intracerebroventricularly reduced suckling-evoked milk ejections.

71 Newborn rat pups tested before suckling experience attached to and ingested milk from t

72 Day (P) 0 and in older neonates with regular suckling experience on P1 or P2.

73 Cesarean-delivered pups tested before suckling experience showed oral grasp responses and inge

74 nerve (CN V), a cranial nerve essential for suckling, feeding and swallowing (S/F/S), a key innate b

75 raniofacial dysfunction as well as disrupted suckling, feeding and swallowing, similar to key 22q11DS

76 Disrupted suckling, feeding, and swallowing from birth onward-peri

77 in 1 activity in the brown adipose tissue of suckling female rats, indicative of increased sympatheti

78 Consistently, suckling first reduced and then increased the expression

79 or lard-rich diet (OHF) during pregnancy and suckling followed by a control diet post-weaning.

80 tes from oral V. cholerae challenge and that suckling from an immunized dam accounts for the majority

81 te utilization in vivo indicated that in the suckling gut B. thetaiotaomicron prefers host-derived po

82 BR3-/- mice exhibited neonatal lethality and suckling impairment that could be partially rescued by l

83 proximately 50% neonatal lethality, impaired suckling in neonatal pups, and loss of LPA responsivity

84 ion of the olfactory cues that trigger first suckling in the mouse would provide the means to determi

85 such as pheromones, acting to promote first suckling in the mouse.

86 In intact animals, suckling increased ERK1/2 activation in the cytosol and

87 Coimmunoprecipitation showed that suckling increased molecular interactions between pERK1/

88 ppressed feeding induced by 24 hr fasting or suckling-induced hyperphagia.

89 ceptor (PRL-R) during lactation is caused by suckling-induced hyperprolactinemia or the suckling stim

90 to both the stimulus of suckling itself and suckling-induced hyperprolactinemia.

91 lactating rats are known to severely reduce suckling-induced kyphosis (upright crouched nursing), wh

92 rthermore, MTII treatment greatly attenuated suckling-induced NPY expression in the DMH.

93 the mediobasal hypothalamus (MBH) regulates suckling-induced prolactin secretion.

94 observed both during parturition and during suckling-induced reflex milk ejection.

95 cerning DAergic neuronal activity during the suckling-induced release of PRL persist.

96 to study mechanisms that evolved to protect suckling infants from SIV infection.

97 Instead, we find that the initiation of suckling is dependent on variable blends of maternal "si

98 They are fully viable probably because suckling is unimpaired, unlike mutants in which the expr

99 Successful suckling is vital to the survival of mammalian newborns.

100 reveals that an apparently innate behavior, suckling, is triggered not by a classical pheromone but

101 y mechanisms related to both the stimulus of suckling itself and suckling-induced hyperprolactinemia.

102 Maternal grooming of young did not vary with suckling location.

103 protection in the gastrointestinal tract of suckling mammals, in the form of secretory IgA (SIgA).

104 did not cause detectable disease in adult or suckling mice after either i.c. or s.c. inoculation.

105 residual murine virulence and is lethal for suckling mice after intracerebral (i.c.) or subcutaneous

106 t 20 microg/mouse afforded 50% protection of suckling mice against challenge with 25 50% lethal doses

107 Also, both Angptl4 -/- suckling mice and adult mice fed a high-fat diet showed

108 lpha is detected in rare epithelial cells of suckling mice and becomes progressively more expressed i

109 50% lethal dose and survival distribution in suckling mice and by histopathology in rhesus monkeys.

110 d that rF257C was attenuated in vivo in both suckling mice and pigs (one of its natural hosts).

111 However, using suckling mice as a model host, we found that intraintest

112 we show that infection of hamster cells and suckling mice by Nodamura virus (NoV), a mosquito-transm

113 e restricted in replication in the brains of suckling mice compared to that of wild-type DEN4, and th

114 ectedly displayed increased pathogenicity in suckling mice compared to wild-type SBV.

115 -membrane vesicles (OMVs) passively protects suckling mice from challenge.

116 tiple IFN types led us to test protection of suckling mice from endotoxin-mediated shock, an outcome

117 us expression of prostasin could protect ICR suckling mice from life-threatening DENV-2 infection.

118 t 2D6 IgA is sufficient to passively protect suckling mice from oral challenge with virulent V. chole

119 mutations were attenuated in s.c. inoculated suckling mice in comparison with TR339.

120 In contrast to observations in suckling mice in which viruses encoding inactivating mut

121 GT knockout (KO) suckling mice infected with SINV strains (AR339 and S.A.

122 s mutation attenuated the virus in 4-day-old suckling mice inoculated by the intracerebral (i.c.) rou

123 at least 28,500 times less neurovirulent in suckling mice inoculated intracerebrally and at least 10

124 SVNI infection of 10-day-old suckling mice led to reduced survival in the knockout mi

125 encephalitis was delayed, a small number of suckling mice still succumbed to lethal intracerebral in

126 Finally, we show using competition assays in suckling mice that inhibition of motility appears to be

127 We studied orally inoculated 5-day-old suckling mice that were deficient in interferon (IFN) si

128 tion of IFN signaling in vivo was studied in suckling mice using the highly infectious murine EW RV s

129 nal and extraintestinal viral replication in suckling mice vary among different heterologous and homo

130 Regulation of MCMV synthesis in these suckling mice was shown to be an IFN-gamma-dependent, pe

131 When suckling mice were infected with RV, they were substanti

132 of Helicobacter pylori infection in infants, suckling mice were inoculated with mixtures of strains t

133 -induced protection was mimicked by treating suckling mice with a glycolipid derived from Helicobacte

134 We show here that infection of ZAP knockout suckling mice with an SVNI led to faster disease progres

135 Herein, we show that infection of suckling mice with influenza A virus protected the mice

136 Infection of suckling mice with influenza virus expands a CD4(-)CD8(-

137 viral RNAi in mouse embryonic stem cells and suckling mice(10,11).

138 ns of NaCl (100 mM or less), and also within suckling mice, a model host for the study of cholera pat

139 y safe following intracranial inoculation of suckling mice, a stringent test of vaccine safety.

140 netics in cell culture, neuroinvasiveness in suckling mice, and ability to replicate and produce diss

141 ly passed EBO-Z virus in progressively older suckling mice, eventually obtaining a plaque-purified vi

142 In suckling mice, exogenously administered type I, II, or I

143 ed EBOV, developed by sequential passages in suckling mice, identified many similarities between this

144 In suckling mice, infection with RV results in an increase

145 ne system is more developed than that of the suckling mice, resulted in significantly improved surviv

146 reased virulence in weanling mice but not in suckling mice, suggesting that specific host conditions

147 , in the developing CNS of highly permissive suckling mice, the miRNA-targeted viruses can revert to

148 Moreover, impairing LRE function in suckling mice, via conditional deletion of Dab2, leads t

149 Finally, in suckling mice, we found two peaks in the CD8 response on

150 virulence after intracerebral inoculation in suckling mice.

151 FMDV plays an important role in virulence in suckling mice.

152 This virus showed growth in HFDK cells and suckling mice.

153 nd such defects were rescued in Rnasel (-/-) suckling mice.

154 e culture, and elicits fluid accumulation in suckling mice.

155 small intestinal epithelial cells (IEC) from suckling mice.

156 over unadapted cells during colonization of suckling mice.

157 cerebrally into the right cortex of C57/BL/6 suckling mice.

158 sets and adoptively transferred into C57BL/6 suckling mice.

159 urovirulent than their parental LGT virus in suckling mice.

160 within intestinal epithelial cells (IECs) of suckling mice.

161 ers in the brains of experimentally infected suckling mice.

162 n to attenuate the neurovirulence of JUNV in suckling mice.

163 rowth and in vivo pathogenicity in adult and suckling mice.

164 ue morphology or its attenuated phenotype in suckling mice.

165 tationary-phase cells were used to inoculate suckling mice.

166 ely restricted intestinal replication in the suckling mice.

167 and mortality compared to wild-type (WT) B6 suckling mice.

168 ter than that of a simian rotavirus (RRV) in suckling mice.

169 RV infection on endotoxin-mediated shock in suckling mice.IMPORTANCE Antiviral functions of types I,

170 ditionally, virus-infected tissue culture or suckling mouse brain (SMB) has been the source of viral

171 ion of 32 pg/0.1 ml, and antigen in infected suckling mouse brain and laboratory-infected mosquito po

172 However, the suckling mouse brain-derived (SMB) antigen used in this

173 sources of virus-infected tissue culture or suckling mouse brain.

174 till use vaccines produced in sheep, goat or suckling mouse brain.

175 lines (Vero, BHK, SW13, and XTC cells) or in suckling mouse brains.

176 El Tor biotype strains throughout the entire suckling mouse GI tract at various times after intragast

177 ype to resist bactericidal mechanisms in the suckling mouse GI tract.

178 The suckling mouse has been used as a model to identify Vibr

179 In fact, the suckling mouse intestine does not appear to be a potent

180 Vibrio cholerae colonization of the suckling mouse intestine is a commonly used animal model

181 Quantitation of RyhB expression in the suckling mouse intestine suggests that iron availability

182 ly uncharacterized environments (such as the suckling mouse intestine) can be used as a reporter of l

183 oH mutant was severely attenuated within the suckling mouse intestine, suggesting that sigma(32)-regu

184 s not required for V. cholerae growth in the suckling mouse intestine.

185 produced normal biofilms, and colonized the suckling mouse intestine.

186 as strains lacking hfq fail to colonize the suckling mouse intestine.

187 ility of results with those for monkeys, the suckling mouse is an appropriate host for safety testing

188 P nor OA is required for colonization of the suckling mouse large bowel.

189 on mutations that affect colonization in the suckling mouse model for cholera.

190 defective for intestinal colonization in the suckling mouse model of cholera and expresses reduced am

191 s in mice and greatly reduced mortality in a suckling mouse model of cholera.

192 on against live V. cholerae challenge in the suckling mouse model of cholera.

193 B could influence protective efficacy in the suckling mouse model of cholera.

194 d whether ribavirin treatment in the lethal, suckling mouse model of HTNV infection would act similar

195 ciently than the wt virus and is lethal in a suckling mouse model of MeV encephalitis even with a low

196 In a suckling mouse model, ectopically stimulating different

197 and III IFN receptors (IFNRs) in vitro In a suckling mouse model, RV effectively blocked STAT1 activ

198 Fbp, and Feo systems was not attenuated in a suckling mouse model, suggesting that at least one other

199 V replication and pathogenesis in an in vivo suckling mouse model.

200 k of HapA did not affect colonization in the suckling mouse model.

201 in preventing intestinal colonization in the suckling mouse model.

202 in cross-linking and fluid accumulation in a suckling mouse model.

203 nd antidiarrheal efficacy in closed-loop and suckling mouse models.

204 TM proteins, were apathogenic in a sensitive suckling mouse neurovirulence test, and were similar in

205 In the suckling mouse, oral inoculation with V. cholerae leads

206 xcellent alternative to the more traditional suckling-mouse brain WN virus antigen used in the immuno

207 Our objective was to determine if suckling neonatal piglets are susceptible to enterohemor

208 apid and more-severe neurological disease in suckling neonates than in those fed an artificial diet.

209 into milk and their passive transfer to the suckling newborn.

210 imulated fluid secretion in the intestine of suckling Nkcc1(-/-) mice were normal.

211 Litters suckling nontransgenic dams succumbed to fatal encephali

212 ctions that help mediate the transition from suckling of a fat-rich diet to independent feeding of a

213 nic mice is sufficient to completely protect suckling offspring against MHV-JHM-induced encephalitis.

214 A comparison of the iron status of suckling offspring from LFKO(-/-) intercrosses and from

215 rough breast milk to the intestinal lumen of suckling offspring, coats the pathogen and reduces intes

216 es in and is transferred through the milk to suckling offspring.

217 ontributions of obesity during pregnancy and suckling on metabolic health post-weaning.

218 r together were required for colonization of suckling or adult mice.

219 om experiments in mitochondria isolated from suckling or adult rats inverted question mark using a di

220 ortion of the mouth in rats that were either suckling or in contact caused a 20-25-s increase in esca

221 reported as a cause of sporadic diarrhea in suckling or weanling pigs, to our knowledge, this is the

222 exogenous glucose administration to actively suckling Oxct1(-/-) mice delayed, but could not prevent,

223 sted from the ceca of these hosts during the suckling period (postnatal day 17) and after weaning (po

224 been observed that SFB are absent during the suckling period and appear in high numbers shortly after

225 e-4 (GPAT4) null pups grew poorly during the suckling period and, as adults, were protected from high

226 A obtained from the mothers' milk during the suckling period and, later, of self-produced sIgA in the

227 -carbohydrate (HC) milk formula during their suckling period developed hyperinsulinemia immediately,

228 Our results demonstrate that the suckling period is critical for epigenetic development o

229 In addition, during the suckling period MG hydrolytic activity is likely to deri

230 During the suckling period until day 14, the piglet breed and the n

231 Mutant pups were severely stunted during the suckling period, but many recovered after weaning.

232 During the suckling period, dams were either fed ad libitum, permit

233 inal stem cells and their progeny during the suckling period, suggesting postnatal epigenetic develop

234 s in hypothalamic DNA methylation during the suckling period, suggesting that it is a critical period

235 other and the breed were evident through the suckling period, the introduction of solid feed and subs

236 rement for any dietary intervention in their suckling period.

237 se to the HC dietary modification during the suckling period.

238 ntestinal epithelial cells is limited to the suckling period.

239 ation and crypt fission during the neonatal (suckling) period, mediated at least in part by changes i

240 he relative contribution of the in utero and suckling periods in establishing the adult offspring phe

241 ostnatal nutrient restriction limited to the suckling phase (50% from postnatal [PN]1 to PN21) (PNGR)

242 re abandoned on the natal site after a brief suckling phase, and must develop foraging skills without

243 In addition, preliminary data suggested that suckling piglets born by a sow immunized with the pLT(19

244 We orally inoculated neonatal, conventional suckling piglets with TC-PC177 or PC21A to compare their

245 ows--an effective means to passively protect suckling piglets.

246 In contrast, suckling PLRP2-deficient mice had fat malabsorption evid

247 t in the intestinal epithelial cells in both suckling pups and adults.

248 r amplified in cells of the immune system of suckling pups nor infected their mammary glands.

249 Chemokines, fed to suckling pups of TNF-deficient mothers, restored both po

250 umor virus (MMTV) is carried from the gut of suckling pups to the mammary glands by lymphocytes and i

251 activity in lactating dams exposed to their suckling pups versus cocaine.

252 expression, as well as expression in vivo in suckling rabbits, is dependent upon RpoS.

253 at of iron and zinc absorption measured by a suckling rat pup model.

254 tion and status in infant rhesus monkeys and suckling rat pups and evaluated differences between inta

255 t of phytate concentration were evaluated in suckling rat pups by using 65Zn and 64Cu.

256 Studies in suckling rat pups showed similar results with no capacit

257 transplanted into the nonpermissive liver of suckling rat pups.

258 In suckling rats < 14 days old, developmental regulation of

259 Using hepatocytes isolated from suckling rats as our model system, we measured CPT I act

260 microg 2.5S NGF into maternally lead-exposed suckling rats on postnatal days P2, P4, P11, or P18.

261 ver ketogenesis in hepatocytes isolated from suckling rats than those from adult rats.

262 ol-binding protein in the small intestine of suckling rats.

263 immunoglobulin G across intestinal cells in suckling rats.

264 Suckling reduced GFAP in immunocytochemical images and i

265 ersisted, though marginal, through postnatal suckling stages of development (1d-21d), with no concomi

266 leased within the lactating rat brain during suckling stimulation and activates specific subcortical

267 ng posture of lactating rats is dependent on suckling stimulation from pups.

268 Suckling stimulation in lactating dams and cocaine expos

269 ctivity in postpartum day 4-8 dams receiving suckling stimulation.

270 re returned to the females to reinitiate the suckling stimulus for 90 min and induce cFos expression.

271 re returned to the females to reinitiate the suckling stimulus for 90 min to induce cFos expression.

272 y suckling-induced hyperprolactinemia or the suckling stimulus itself.

273 these areas is most likely regulated by the suckling stimulus itself.

274 part due to neural impulses arising from the suckling stimulus.

275 lactating animals that were activated by the suckling stimulus.

276 by hyperprolactinemia in the presence of the suckling stimulus.

277 due to the neural impulses arising from the suckling stimulus.

278 tration of DA and DOPAC of the IL due to the suckling stimulus.

279 ncentration of DOPAC was detected due to the suckling stimulus.

280 ncentration of plasma PRL in response to the suckling stimulus.

281 Suckling-sucrose treatment significantly reduced Fos-LI

282 In the suckling systems the flux control coefficients for CPT I

283 These data indicate that after suckling terminates, TH up-regulation is evident at 1.5

284 ts, have been selected to favor more intense suckling than genes of maternal origin.

285 Secondly after a prolonged absence of suckling, the consequent decline in circulating lactogen

286 y energy expenditure, milk energy output and suckling time were all lower at 30 degrees C.

287 after birth, all mammals must initiate milk suckling to survive.

288 otein-sensitized cells from animals 10 days (sucklings) to 12 weeks (young adults) of age.

289 ferentiation and renewal, nor does it affect suckling-to-weaning transition.

290 umbed to fatal encephalitis, whereas litters suckling transgenic dams were fully protected against ch

291 bout the effects of different feeding modes (suckling versus bottle-feeding) or microbial sources on

292 , the first pheromone sufficient to initiate suckling was isolated from the rabbit.

293 We show here that suckling-weaning and fasting-refeeding transitions in ro

294 complex to the SIF3 element both during the suckling-weaning developmental transition and Caco-2 cel

295 all intestinal villous epithelium during the suckling-weaning transition in mice.

296 d in the villous epithelial cells during the suckling-weaning transition.

297 with CONV-R gut microbiota at the end of the suckling-weaning transition.

298 for the surviving pups were 60-80% of those suckling wild-type mice.

299 In lactating rats, oxytocin cells respond to suckling with brief, explosive, synchronous bursts of el

300 transfer of antibody from mother to fetus to suckling young.