ライフサイエンスコーパス: pair bond

1 athways interact in the establishment of the pair bond.

2 onditioned partner preference, observed as a pair bond.

3 ng that is necessary to maintain the initial pair bond.

4 n, expression, and maintenance of monogamous pair bonds.

5 n species differences in the ability to form pair bonds.

6 productive activation or to the formation of pair bonds.

7 anges that result in the formation of stable pair bonds.

8 attributed to paternal provisioning based on pair bonds.

9 er pairs typically show strong and selective pair bonds.

10 ion (STI) in populations with such ephemeral pair bonds.

11 ial sex differences in the CRF modulation of pair bonding.

12 nsible for the enduring nature of monogamous pair bonding.

13 thin these subregions differentially mediate pair bonding.

14 ned the effects of repeated AMPH exposure on pair bonding.

15 direct evidence for epigenetic regulation of pair-bonding.

16 tion of selective aggression associated with pair-bonding.

17 We propose that long-term pair bonds, affinal kin recognition, exogamy, and multi-

18 ike many other rodents, they are gregarious, pair bond after copulating, and are biparental.

19 ocially monogamous rodent species that forms pair bonds after mating, a behavior in which central dop

20 ially monogamous rodent that forms long-term pair bonds after mating--we demonstrate that amphetamine

21 contributes to the neuroprotective effect of pair bonding against drug reward.

22 ful of primates that, like humans, routinely pair bond and care cooperatively for their young.

23 aracterized their aggression associated with pair bonding and examined the related neuronal activatio

24 ributors to the effects of VP-OT peptides on pair bonding and gregariousness; reveal previously unkno

25 mine receptor subtype-specific influences on pair bonding and how dopamine receptor activation may in

26 d with female reproductive behaviors such as pair bonding and kin recognition.

27 e evolution of OT's female-specific roles in pair bonding and maternal functions.

28 s to examine the effects of drug exposure on pair bonding and related neural circuitry.

29 overlap between the processes that underlie pair bonding and those that mediate responses to abused

30 reeding grounds is important for maintaining pair bonds and is achieved by pairs that remain together

31 y predicts that in species lacking long-term pair bonds and menopause, males should not exhibit a pre

32 g in general and the stability of monogamous pair bonds and offspring care in particular.

33 appear to be important for the initiation of pair bonds and parental behaviors as well as the infant'

34 tion that ASR influences multiple aspects of pair-bond and mating behavior in wild populations.

35 Unbalanced ASRs are predicted to influence pair-bond and mating behavior, since the rarer sex in th

36 Our results suggest that pair-bonding and increased sex egalitarianism in human e

37 ociation between variation in OXTR and human pair-bonding and other social behaviors, possibly indica

38 cin receptor gene (OXTR) are associated with pair-bonding and related social behaviors in humans.

39 uptake were found between males in long-term pair-bonds and lone males in areas including the nucleus

40 on, (c) motivation for parental behavior and pair bonding, and (d) the neural consequences of social

41 female-specific deficits in gregariousness, pair bonding, and nest cup ownership; reduces side-by-si

42 ebrate taxa, focusing on female mate choice, pair-bonding, and aggressive behavior.

43 Short-term pair bonds are also associated with unbalanced ASRs: mal

44 ch individuals form pairs just to mate (i.e. pair bonds are ephemeral) and later move on to sexually

45 plicated in increased partner preference and pair bonding behavior in mammalian lineages.

46 ial problems, which longitudinally predicted pair-bonding behavior in the TCHAD sample.

47 1240), comprising measures of self-reported pair-bonding behavior.

48 in plays a central role in the regulation of pair-bonding behavior.

49 cus of such research, especially its role in pair bonding between mates in species that display monog

50 cially monogamous rodent that forms enduring pair bonds between adult mates.

51 g the formation and maintenance of selective pair bonds between mates.

52 of human origins is the emergence of strong pair-bonding between males and females accompanied by a

53 h levels of affiliative behaviors, including pair-bonding, biparental care, and cooperative breeding.

54 ions and beyond the mother-offspring, kin or pair bond broadens the generality of the social bufferin

55 te change by pair members and/or breaking of pair bonds by unmated individuals is more frequent when

56 The formation of monogamous pair bonds, by prairie voles, is facilitated by activati

57 In the laboratory, pair bonds can be assessed by testing for a partner pref

58 chrogaster) are monogamous rodents that form pair bonds characterized by a preference for a familiar

59 ominent scenarios of the human transition to pair-bonding: communal care, mate guarding, food for mat

60 (i.e., alpha-helix N conformation, DNA base pair bonding, conformation of protein residues in the vi

61 How such a transition from promiscuity to pair-bonding could be achieved is puzzling.

62 effects are observed for social preferences, pair bonding, courtship, maintenance behaviors, or anxie

63 gitudinal relationship between precursors of pair-bonding during childhood and subsequent behavior in

64 Together, our data demonstrate that pair-bonding experience decreases the rewarding properti

65 Males that were pair-bonded for 2 weeks displayed intense levels of aggr

66 are mediated by neural mechanisms regulating pair bond formation and not alcohol's effects on mating,

67 cies differences in the behaviors, including pair bond formation and paternal care, found selectively

68 potential role for CART in the regulation of pair bond formation between monogamous mates and suggest

69 se data demonstrate opposing regulation over pair bond formation by cAMP signaling within the NAcc sh

70 ing that AVP in the lateral septum regulates pair bond formation in male prairie voles and that this

71 Reward mechanisms are involved in pair bond formation in monogamous prairie voles.

72 es of action for CRF-induced facilitation of pair bond formation in prairie voles, as well as potenti

73 interaction of these circuits in a model of pair bond formation in rodents with a discussion of the

74 the regulation of alloparental behavior and pair bond formation in the socially monogamous prairie v

75 ich receptors in these brain regions mediate pair bond formation in this monogamous species.

76 ntagonist in the lateral septum also blocked pair bond formation induced by either mating or AVP admi

77 tested the hypothesis that DA regulation of pair bond formation is mediated via the cAMP signaling c

78 how that dopamine transmission that promotes pair bond formation occurs within the rostral shell of t

79 the dorsomedial NAc shell appear to mediate pair bond formation through the positive hedonics associ

80 ve affiliation between adult mates, known as pair bond formation, as assessed by partner preference i

81 knowledge of central dopamine involvement in pair bond formation, expression, and maintenance.

82 posite effects: D1-like activation prevented pair bond formation, whereas D2-like activation facilita

83 of maintaining signals of quality well after pair bond formation.

84 t AVP in the lateral septum is important for pair bond formation.

85 ction, and the subsequent mating facilitates pair bond formation.

86 uitry during social interactions facilitates pair bond formation.

87 e distinct subregions differentially mediate pair bond formation.

88 in the NAcc, resulting in the impairment of pair bond formation.

89 gh dopamine is necessary for mammalian adult pair-bond formation and maternal behavior, its function

90 A neurobiological model for pair-bond formation has emerged from studies in monogamo

91 the hypothesis that NAcc DA is critical for pair-bond formation in male prairie voles.

92 ogamy, as oxytocin and vasopressin influence pair-bond formation in the monogamous species.

93 that V1aR activation in this region promotes pair-bond formation via a mechanism similar to condition

94 familiar opposite-sex partner, used to index pair-bond formation) by male voles.

95 ehaviors associated with monogamy, including pair-bond formation, are facilitated by the neuropeptide

96 icetines that differ in the extent of social pair-bond formation, Siberian (Phodopus sungorus) and Dj

97 that the mate-guarding hypothesis for human pair bonds gains strength from explicit links with our g

98 a monogamous rodent that forms long-lasting pair bonds, has proven useful for the neurobiological st

99 eronasal organ (VNO) in estrus induction and pair bonding in female prairie voles.

100 ation of enduring aggression associated with pair bonding in male prairie voles.

101 costerone and central CRF receptors modulate pair bonding in the monogamous prairie vole.

102 ssociated with the formation of opposite-sex pair bonds in microtine rodents.

103 T) receptors (OTRs) impairs the formation of pair bonds in prairie voles (Microtus ochrogaster) and z

104 rain play critical roles in the formation of pair bonds in the monogamous prairie vole.

105 n OXTR was associated with traits reflecting pair-bonding in women in the TOSS and TCHAD samples.

106 ormation of partner preferences (an index of pair bonding) in female prairie voles.

107 rence (PP) formation (a laboratory proxy for pair bonding) in socially monogamous prairie voles (Micr

108 results based on assuming long-term, stable pair bonds, in which case one is capable of preventing o

109 Microtus ochrogaster) display mating-induced pair bonding indicated by social affiliation with their

110 ting behavior: divorce, social polygamy, and pair-bond infidelity.

111 Adult pair bonding involves dramatic changes in the perception

112 The establishment of a pair bond is associated with a behavioral transition fro

113 and the subsequent development of monogamous pair-bonds is substantially predicted by influential imp

114 to forgoing access to resources, maintaining pair bonds led individuals to develop a flexible "scroun

115 ogenous opioid systems, opiate regulation of pair bond maintenance has never been studied.

116 le, male voles showed behavior indicative of pair bond maintenance-namely, selective aggression towar

117 erstanding of neural mechanisms that mediate pair bond maintenance.

118 rsive social motivation that is critical for pair bond maintenance.

119 attractive because humans maintain long-term pair bonds, making reproductive value (i.e. future repro

120 Pair-bonded male prairie voles (Microtus ochrogaster) we

121 re we show that this selective aggression in pair-bonded male prairie voles is associated with increa

122 nctional MRI experiment with 20 heterosexual pair-bonded male volunteers.

123 After pair-bonding, male prairie voles (Microtus ochrogaster)

124 Twelve pair-bonded males (including six with a lesion of the pr

125 Pair-bonded males also showed an increased density in V1

126 blockade diminished selective aggression in pair-bonded males.

127 ) with the option to provide food rewards to pair-bonded mates.

128 involves significant cooperation, selective pair-bonds may develop between 2 nestmates.

129 showed better visual acuity than that of the pair-bonding, monogamous X. flavipinnis.

130 Rodent studies have focused on pair-bonded, opposite-sex mates and suggest that a varie

131 P in the regulation of aggression induced by pair-bonding or drug experience in socially monogamous m

132 ehaviors associated with monogamy, including pair bonding, paternal care and mate guarding.

133 erence (CPP) in sexually naive (SN), but not pair-bonded (PB), males.

134 Pair-bonded prairie voles (Microtus ochrogaster) are bip

135 dimorphic involvement of stress hormones in pair bonding provides a proximate mechanism for regulati

136 We show that the 002 pair bonds rapidly under a wide range of conditions and

137 ed potential epigenetic mechanisms mediating pair-bond regulation and found that the histone deacetyl

138 ASR is strongly correlated with long-term pair bonds, since the divorce rate is higher in species

139 We investigated the sensitivity of jackdaws, pair-bonded social corvids that exhibit an analogous eye

140 s complex mammalian social behaviors such as pair bonding, social recognition and aggression causally

141 tioned stimulus) while potentially promoting pair-bonding, social memory and parental care.

142 this structure is crucial for mating-induced pair bonding, suggesting an important role for the VNO i

143 ghly social, monogamous species and displays pair bonding that can be assessed by the presence of sel

144 crotus ochrogaster), mating induces enduring pair-bonds that are initiated by partner preference form

145 suggest that repeated AMPH exposure impairs pair bonding through an OT-mediated mechanism, and that

146 rgument that connects the evolution of human pair bonds to the male-biased mating sex ratios that acc

147 For both sexes, we show that pair bonding up-regulates mRNA expression for genes enco

148 a partner preference, a choice test in which pair-bonded voles regularly prefer their partner to a co

149 ccumbens in the formation and maintenance of pair bonds was assessed in a series of experiments using

150 e bonding was attributed to the reduced lone pair bond weakening effect, LPBWE, upon substitutions wi

151 sioned females failed to show mating-induced pair bonding whereas intact and sham-lesioned females di

152 cies of vole, one of which is monogamous and pair bonds whereas the other species is promiscuous and

153 in the lateral septum blocked mating-induced pair bonding, whereas administration of AVP induced this

154 Prairie vole breeder pairs form monogamous pair bonds, which are maintained through the expression

155 prairie voles (Microtus ochrogaster) form a pair bond with a female partner after mating, and this b

156 ormation of a sigma-complex through electron-paired bonding within the triplet manifold.