ライフサイエンスコーパス: vole

1 is the alternate cusp offset present in the vole.

2 formation in the socially monogamous prairie vole.

3 to the specialized life style of the prairie vole.

4 us vole species, the meadow vole and montane vole.

5 ulate pair bonding in the monogamous prairie vole.

6 of experiments using the monogamous prairie vole.

7 tion of pair bonds in the monogamous prairie vole.

8 ects of estrogen on the brain of the prairie vole.

9 eptor (V1aR)] antagonist in the male prairie vole.

10 e vole, but not in the non-monogamous meadow vole.

11 species of mammalian research, and the bank vole.

12 between prairie voles and polygamous meadow voles.

13 quences on social behavior in female prairie voles.

14 effects of AMPH treatment in female prairie voles.

15 scles in adult male, but not female, prairie voles.

16 rence would be similarly distinct in prairie voles.

17 perience in socially monogamous male prairie voles.

18 ed in an unknown wild mammal, probably field voles.

19 ty and social behavior in prairie and meadow voles.

20 associated with pair bonding in male prairie voles.

21 s found in a chemosensory pathway in prairie voles.

22 rdU) in the amygdala and DG than did prairie voles.

23 but not in the pMeA or DG, than did prairie voles.

24 oles compared to congener promiscuous meadow voles.

25 in pair bond formation in monogamous prairie voles.

26 l (pMeA) nuclei, in meadow, but not prairie, voles.

27 ve reproductive phenotypes among male meadow voles.

28 tor (V1aR) in a large sample of wild prairie voles.

29 ical for pair-bond formation in male prairie voles.

30 d selective social behaviors in male prairie voles.

31 n the preference for hind nipples in prairie voles.

32 xtended amygdala than asocial, nonmonogamous voles.

33 induction and pair bonding in female prairie voles.

34 g throughout the forebrain of female prairie voles.

35 r the VNO in reproductive success in prairie voles.

36 n the ventral pallial region of male prairie voles.

37 trasted them with comparable data for cyclic voles.

38 he mediation of social attachments in female voles.

39 c oxide synthase (nNOS) in lactating prairie voles.

40 formation of a partner preference in female voles.

41 production of maternal aggression in prairie voles.

42 nal and mating-induced aggression in prairie voles.

43 he control of maternal aggression in prairie voles.

44 tcopulatory aggression in adult male prairie voles.

45 pecies, including monogamous and promiscuous voles.

46 of PUUV-infected and uninfected female bank voles.

47 (an index of pair bonding) in female prairie voles.

48 s distribution in this population of prairie voles.

49 , used to index pair-bond formation) by male voles.

50 rent neurobiological actions in male prairie voles.

51 er immunocompetence (NBT) than did wild-born voles.

52 itry mediate selective aggression in prairie voles.

53 Using a large compilation of time series of vole abundances, we demonstrate consistent cycle amplitu

54 In male voles, all 3 drugs had an inverted-U dose-response curve

55 Prairie voles also match the fear response, anxiety-related beha

56 These voles also showed a significant upregulation in nucleus

57 with paternal care in consistently paternal voles, also may be associated with paternal care (when p

58 conserved neural mechanisms between prairie vole and human.

59 g differences between the monogamous prairie vole and its promiscuous congeners.

60 and two promiscuous vole species, the meadow vole and montane vole.

61 of two monogamous vole species, the prairie vole and pine vole, and two promiscuous vole species, th

62 In specific vole and primate species the neuropeptide oxytocin plays

63 A distinct patterning difference between the vole and the mouse molars is the alternate cusp offset p

64 galitarian and monogamous ones, like prairie voles and humans, when there is no perceived cost to sel

65 a-IR in the MeA than male montane and meadow voles and in the BST relative to montane males.

66 to deteriorating extrinsic conditions (fewer voles and more goshawks), owls appeared to breed more fr

67 e expression have been found between prairie voles and polygamous meadow voles.

68 ehavior parallel differences between prairie voles and promiscuous congeners.

69 rnal aggression and NO production in prairie voles and suggest that the central release of NO may pla

70 egulates pair bond formation in male prairie voles and that this process requires access to both AVP

71 tus montanus) and meadow (M. pennsylvanicus) voles and the monogamous pine vole (M. pinetorum), and t

72 atural variation in food availability (field vole) and predator abundance (northern goshawk) to quant

73 mous vole species, the prairie vole and pine vole, and two promiscuous vole species, the meadow vole

74 behavioral effects of AMPH in female prairie voles, and found that conditioning with low to intermedi

75 renting in juvenile and adult female prairie voles, and oxytocin receptor antagonist infused into the

76 ion of partner preferences in female prairie voles, and suggest that oxytocin receptor expression in

77 Here, we show that prairie voles are susceptible to mule deer CWD prions in vivo an

78 cilitation of pair bond formation in prairie voles, as well as potential sex differences in the CRF m

79 n on partner preference formation in prairie voles, as well as the interaction between the MC and OT

80 efined site quality from the survivorship of voles at the sites and the time at which they commenced

81 nd RMRt of 75 free-living short-tailed field voles at two time points in late winter.

82 In socially monogamous male prairie voles, AVP acts centrally via vasopressin V1a receptor (

83 rmation of social attachment in male prairie voles, because administration of haloperidol blocked, wh

84 tion) as proxies for animal welfare in water voles being reintroduced to the Upper Thames region, Oxf

85 licated by the fact that OTRs in finches and voles bind not only forms of OT, but also vasopressin (V

86 In male prairie voles, both vasopressin and dopamine act in the ventral

87 nd that sPMCA amplification of CWD prions in vole brain enhances the infectivity of CWD for this spec

88 ons, the distribution pattern of BDNF in the vole brain generally resembled the pattern found in rats

89 alization of estrogen receptors in the adult vole brain.

90 appa- and mu-opioid receptors in the prairie vole brain.

91 Prairie vole breeder pairs form monogamous pair bonds, which are

92 partner preference formation in the prairie vole, but not in the non-monogamous meadow vole.

93 e BST of male and female hamsters and meadow voles, but not in rats.

94 in male and female hamsters and male meadow voles, but not rats.

95 ding to residues 120-144 of human (Hu), bank vole (BV), and Syrian hamster (SHa) prion protein, from

96 Interestingly, bank voles (BV) exhibit an unprecedented promiscuity for dive

97 formation in the socially promiscuous meadow vole by using viral vector V1aR gene transfer into the v

98 was not facilitated in nonmonogamous meadow voles by introducing oxytocin receptor into the nucleus

99 atric disorders, discoveries made in prairie voles can direct novel treatment strategies for disorder

100 rtain PrP(C) sequences, such as that of bank vole, can be converted by a remarkably broad array of di

101 Likewise, in adult male prairie voles, central (intracerebroventricular) injections of A

102 A-seq, we show that another rodent, the bank vole Clethrionomys glareolus, possesses three transcript

103 study, field voles (Microtus agrestis), bank voles (Clethrionomys glareolus), and wood mice (Apodemus

104 We found high frequencies of cataracts in voles collected from different areas in Chernobyl.

105 redator (tawny owl) and its main prey (field vole) collected in Kielder Forest (UK) where vole dynami

106 o be disproportionately large in the prairie vole compared with other rodents.

107 CART mRNA and peptide in monogamous prairie voles compared to congener promiscuous meadow voles.

108 uence of oxytocin on affiliative behavior in voles could also be of importance for humans.

109 we also observed striking sex differences in voles: CRFR(2) binding was higher in the encapsulated be

110 ors are likely to be threatened by dampening vole cycles throughout Europe.

111 We found the observed dampening vole cycles, characterized by low spring densities, dras

112 were sought from the extensive literature on vole cycles.

113 glings were higher in years with high spring vole densities and negative wNAO (i.e. colder and drier

114 d adult survival were positively affected by vole density in autumn but relatively insensitive to wNA

115 Breeding propensity increased with vole density, although increasing goshawk abundance redu

116 a support the hypothesis that captive meadow voles develop selective and enduring same-sex social bon

117 Male and female montane voles did not differ.

118 hydration and body condition of captive-bred voles differed between their pre-release measures and bo

119 of PrP (PrP(RES)) in the brains of affected voles differed from those in cervidized transgenic (CerP

120 Male and female meadow voles differed in the ventromedial hypothalamus, with fe

121 s experiments were performed on male prairie voles displaying affiliation or aggression.

122 vole) collected in Kielder Forest (UK) where vole dynamics shifted from a high- to a low-amplitude fl

123 These results suggest that other vole-eating predators are likely to be threatened by dam

124 However, its impact on guilds of vole-eating predators remains unknown.

125 dministration in sexually naive male prairie voles enhanced V1aR expression in the AH and induced agg

126 Both male and female voles exhibit alloparental behavior, but its neurobiolog

127 In female prairie voles, exposure to a male or to male sensory cues is ess

128 indicate that, in both male and female pine voles, exposure to an opposite-sex conspecific is suffic

129 Male pine voles expressed lower levels of ERalpha-IR in the MeA th

130 s asparagine at position 170, our red-backed voles expressed serine and refute previous suggestions t

131 from four closely related species of common vole (field mouse), Microtus arvalis.

132 Meadow voles had a higher density of cells labeled with the cel

133 Virgin male prairie voles had a large number of TH-immunoreactive cells in a

134 Virgin female prairie voles had far fewer TH-immunoreactive cells in these sit

135 Meadow voles had more ERalpha-labeled cells in the pCorA and VM

136 Both OT and OTA voles had significantly higher levels of social contact

137 Bank voles have a high number of Asn and Gln residues and a h

138 Furthermore, prairie voles have higher densities of oxytocin receptors in the

139 Social, monogamous voles have more OT receptors in the extended amygdala th

140 Comparative studies in voles have suggested that a polymorphic microsatellite u

141 The bank vole HBA-T3 gene is distinguished from each HBA-T1 and H

142 on relaxation of purifying selection on bank vole HBA-T3.

143 nt influences CART expression in the prairie vole in a region- and stimulus-specific manner.

144 ch, the author observed 8 litters of prairie voles in a seminatural environment to confirm the prefer

145 in forebrain V1aR expression of male prairie voles in mixed-sex seminatural enclosures.

146 and site quality suggested that in February voles in poorer sites had higher energy demands, indicat

147 The LVs were isolated from bank voles in Sweden during a search for an infectious agent

148 lates were distinct from those isolated from voles in the 1930s in Great Britain, they had a high deg

149 rtner preference formation in female prairie voles in the absence of mating.

150 ticus (wood mice) and Myodes glareolus (bank voles) in the UK and confirmed that several Bartonella s

151 highly conserved between prairie and meadow voles, including many subnuclei examined within the hypo

152 on and impair social bonding in male prairie voles) increased D1, but not D2, receptor mRNA in the NA

153 In addition, voles inoculated orally with sPMCA products developed cl

154 Prairie voles inoculated with sPMCA products developed clinical

155 The prairie vole is a socially monogamous rodent that is an excellen

156 The prairie vole is a socially monogamous species in which breeder p

157 Unlike most mammalian species, the prairie vole is highly affiliative, forms enduring social bonds

158 of the natural red colouration in adult bank voles is affected by ionizing background radiation, and

159 ctive aggression in pair-bonded male prairie voles is associated with increased release of vasopressi

160 rmation of monogamous pair bonds, by prairie voles, is facilitated by activation of dopamine (DA) D2-

161 Among monogamous prairie voles, levels of vasopressin receptor (encoded by the ge

162 ennsylvanicus) voles and the monogamous pine vole (M. pinetorum), and two species of cricetines that

163 uce distinct pathological phenotypes in bank voles (M. glareolus), irrespective of the presence of 21

164 re harbored within the nuclear genome of the vole Microtus rossiaemeridionalis.

165 established the socially monogamous prairie vole (Microtus ochrogaster) as an animal model with whic

166 The prairie vole (Microtus ochrogaster) exhibits parental behavior i

167 The prairie vole (Microtus ochrogaster) is a highly social, monogamo

168 The prairie vole (Microtus ochrogaster) is a socially monogamous rod

169 Here we show, using a prairie vole (Microtus ochrogaster) model of social bonding, how

170 The prairie vole (Microtus ochrogaster), a monogamous rodent that fo

171 asal OT given developmentally in the prairie vole (Microtus ochrogaster), a socially monogamous roden

172 es, the highly social and monogamous prairie vole (Microtus ochrogaster), greatly increases partner-d

173 In the socially monogamous prairie vole (Microtus ochrogaster), mating induces enduring pai

174 Using the prairie vole (Microtus ochrogaster)--a socially monogamous roden

175 g-induced social deficits, using the prairie vole (Microtus ochrogaster)-a socially monogamous rodent

176 ocial attachment of the "monogamous" prairie vole (Microtus orchrogaster).

177 In this study, field voles (Microtus agrestis), bank voles (Clethrionomys gla

178 Relative abundance of voles (Microtus mexicanus) increased in exclosure draina

179 ssion of pro-social behavior in male prairie voles (Microtus ochragaster), predicting that inhibition

180 es sympatric with cervids, including prairie voles (Microtus ochrogaster) and field mice (Peromyscus

181 pairs the formation of pair bonds in prairie voles (Microtus ochrogaster) and zebra finches (Taenioyp

182 Prairie voles (Microtus ochrogaster) are a valuable model for st

183 Pair-bonded prairie voles (Microtus ochrogaster) are biparental after the bi

184 Prairie voles (Microtus ochrogaster) are exceptional among roden

185 Prairie voles (Microtus ochrogaster) are monogamous and, like hu

186 Prairie voles (Microtus ochrogaster) are monogamous rodents that

187 Although prairie voles (Microtus ochrogaster) are socially monogamous, ma

188 somatosensory cortex was examined in prairie voles (Microtus ochrogaster) by using electrophysiologic

189 After pair-bonding, male prairie voles (Microtus ochrogaster) display aggression toward n

190 Male prairie voles (Microtus ochrogaster) display mating-induced pair

191 Prairie voles (Microtus ochrogaster) exhibit a monogamous social

192 Male prairie voles (Microtus ochrogaster) form a pair bond with a fem

193 mmunoreactivity (IR) was compared in prairie voles (Microtus ochrogaster) from Illinois (IL), which a

194 Male prairie voles (Microtus ochrogaster) spontaneously exhibit high

195 The authors exposed male prairie voles (Microtus ochrogaster) to novel females in a multi

196 n of sexually nai;ve male and female prairie voles (Microtus ochrogaster) triggers a cascade of physi

197 Female prairie voles (Microtus ochrogaster) were exposed to 1 hour immo

198 Pair-bonded male prairie voles (Microtus ochrogaster) were infused with a retrogr

199 were used to enhance ERalpha in male prairie voles (Microtus ochrogaster), which display high levels

200 to form a partner preference in male prairie voles (Microtus ochrogaster).

201 pair bonding) in socially monogamous prairie voles (Microtus ochrogaster).

202 socioreproductive behaviors in male prairie voles (Microtus ochrogaster).

203 and population dynamics were studied in root voles (Microtus oeconomus).

204 re in nature, whereas closely related meadow voles (Microtus pennsylvanicus) are solitary and polygam

205 Female meadow voles (Microtus pennsylvanicus) are territorial during w

206 Nonmonogamous meadow voles (Microtus pennsylvanicus), which exhibit seasonal

207 competition, respectively, among male meadow voles (Microtus pennsylvanicus).

208 rentally inexperienced or experienced meadow voles (Microtus pennsylvanicus).

209 ial transmission of food preferences in pine voles (Microtus pinetorum) and whether food items had to

210 Paternal and nonpaternal voles (microtus) have different arginine-vasopressin (AV

211 In voles (Microtus), central oxytocin (OT) receptor pattern

212 of a 25-year study of the monogamous prairie vole, Microtus ochrogaster, in Illinois, USA.

213 In the creeping vole, Microtus oregoni, females are X0 and males are XY.

214 In prairie voles, Microtus ochrogaster, females exhibit a dramatic

215 In monogamous prairie voles, Microtus ochrogaster, males are parental and exhi

216 Here we show that male meadow voles, Microtus pennsylvanicus, increase their sperm inv

217 Vole molars cultured without the braces lose their cusp

218 ncies of cataracts are found in eyes of bank voles Myodes glareolus collected from natural population

219 radiation among natural populations of bank voles Myodes glareolus in Chernobyl affected expression

220 mother and offspring condition, in the bank vole (Myodes glareolus).

221 Group sizes varied from 8 to 15 voles (n = 89 voles total).

222 Group sizes varied from 6 to 8 voles (N = 98 total).

223 ons of DA neuroanatomy and tissue content in vole NAcc, and mating appeared to induce a 33% increase

224 ded conversion of PrP(c), but human and bank vole NTDs did the opposite.

225 After interacting with a demonstrator vole, observer voles preferred cocoa-flavored food as co

226 advanced by the findings from two species of vole, one of which is monogamous and pair bonds whereas

227 In monogamous prairie voles, OT and dopamine interact to promote partner prefe

228 TH-immunoreactive cells in the male prairie vole pBST and MeAPd, an effect that could be reversed wi

229 We find that vole peaks are blunt, consistent with their cycles being

230 length of 2-5 yr, peak densities of 100-350 voles per ha and trough densities of 0-25 ha(-1), ratio

231 Continent-scale dampening of vole population cycles, keystone herbivores in many ecos

232 occurrence of a catastrophic collapse in the vole population followed by a prolonged low phase.

233 Within the normal prairie vole population, both the type and the amount of interac

234 teracting with a demonstrator vole, observer voles preferred cocoa-flavored food as compared with eit

235 or diverse prion isolates, arguing that bank vole PrP (BVPrP) may be inherently prone to adopting mis

236 the amino-terminal domain of human and bank vole PrP(c)s requires interaction with the rest of the m

237 facilitates conversion of the human and bank vole PrP(c)s to the prion forms.

238 Additionally, full-length human and bank vole PrP(c)s were more likely to be converted to amyloid

239 do not promote the propagation of mouse and vole PrP(Sc) molecules.

240 Prairie vole pups (Microtus ochrogaster) in laboratory cages pre

241 Prairie vole pups in seminatural environments preferred hind nip

242 Adult male prairie voles received a sham surgery, were gonadectomized, or w

243 sterone, a stress hormone, in female prairie voles recovering alone but not the female prairie voles

244 In addition, we treated immobilized female voles recovering alone with oxytocin or vehicle and fema

245 ng alone with oxytocin or vehicle and female voles recovering with their male partner with a selectiv

246 recovering alone but not the female prairie voles recovering with their male partner.

247 eference, a choice test in which pair-bonded voles regularly prefer their partner to a conspecific st

248 of OT directly into the mPFC of AMPH-exposed voles restored partner preferences, and altered NAcc DA

249 er extended cohabitation with a female, male voles showed behavior indicative of pair bond maintenanc

250 f Xist gene structure both between different vole species and relative to mouse and human Xist/XIST.

251 Further examination of CRF receptors in vole species may reveal a novel role for CRF in social b

252 of change throughout Europe and grass-eating vole species suggests a common climatic driver.

253 ; the onset of disease was faster in the two vole species than the two Peromyscus spp.

254 irie vole and pine vole, and two promiscuous vole species, the meadow vole and montane vole.

255 and CRFR(2) in the brains of two monogamous vole species, the prairie vole and pine vole, and two pr

256 forebrain of monogamous than in promiscuous vole species, whereas dopamine receptor distribution is

257 microsatellite structure and monogamy in 21 vole species.

258 erminalis in males than females for all four vole species.

259 inding densities, as is the case in multiple vole species.

260 ation, sexual differentiation of the prairie vole spinal cord differs from that found in most other l

261 Studies of rats and voles suggest that distinct pathways emanating from the

262 y, these data are consistent with reports in voles suggesting that the combined disruption of SCN and

263 hat had not interacted with demonstrators or voles that had been exposed to odors.

264 -flavored food as compared with either naive voles that had not interacted with demonstrators or vole

265 Adult female prairie voles that overexpress oxytocin receptor in the nucleus

266 Ovariectomized prairie voles that were treated with estradiol benzoate had a hi

267 eus of the amygdala, than did ovariectomized voles that were treated with vehicle.

268 vioral consequences of exposing male prairie voles to a pup.

269 Here, we used male prairie voles to examine the effects of drug exposure on pair bo

270 udy, we confirm the unique susceptibility of voles to infection with M. microti and the relative resi

271 We housed male-female pairs of pine voles together for 0, 2, 6, 12, or 24 h before collectin

272 roup sizes varied from 8 to 15 voles (n = 89 voles total).

273 In prairie voles, trade-offs in the fitness consequences of social

274 Few studies of vole tuberculosis have been undertaken since then, and l

275 Mycobacterium microti (vole tuberculosis) infections in small wild mammals were

276 We monitored a natural population of field voles using longitudinal and cross-sectional sampling mo

277 crosatellite in the 5' region of the prairie vole vasopressin 1a receptor (avpr1a) gene modify gene e

278 ow the behavioral repertoire of male prairie voles via a DA receptor-specific mechanism in the NAcc,

279 A demonstrator vole was fed cocoa-flavored food, a nonpreferred food.

280 and six nuclear markers in Myodes glareolus voles was examined, including populations that show mtDN

281 A group of gonadally intact female prairie voles was included to reveal possible sex differences.

282 rthermore, the number of offspring in female voles was negatively correlated with cataract severity.

283 Here, male prairie voles were administered intracerebroventricularly a V1aR

284 Captive-bred voles were assessed pre-release, and each month post-rel

285 Wild-born voles were captured in the field and assessed from two m

286 ochrogaster) and meadow (M. pennsylvanicus) voles were compared to examine neural cell proliferation

287 e parental behavior of virgin female prairie voles were examined.

288 Reproductively naive, adult male prairie voles were implanted with radiotransmitters used for rec

289 Male and female adult prairie voles were placed in a cage either alone, or with a nove

290 Adult male prairie voles were transfected with ERalpha in the MeA (MeA-ERal

291 formation of a partner preference in mating voles, whereas the D2 agonist quinpirole facilitated for

292 igated Oxtr expression in monogamous prairie voles, which have a well-characterized OXT system.

293 and genomic tools for this species, prairie voles will likely maintain their current trajectory beco

294 n acute increases in social behavior in male voles with familiar partners, as seen in humans.

295 ehavioral testing of female and male prairie voles with immunohistochemistry for citrulline, a marker

296 We treated voles with one of three dosages of intranasal OT, or sal

297 Overall, our data indicate that the prairie vole would be a useful model for exploring how individua

298 othesized that PR expression in male prairie voles would differ from that described in other male rod

299 Comparative research in voles yields a model based on interspecies and intraspec

300 Prairie vole young on hind nipples, however, were dislodged less