ライフサイエンスコーパス: maternal behavior

1 area (mPOA, an area important in display of maternal behaviors).

2 ones could reduce such activity to stimulate maternal behavior.

3 MPOA was previously shown to be critical for maternal behavior.

4 d several medial hypothalamic sites, inhibit maternal behavior.

5 ontinual exposure of females to pups induces maternal behavior.

6 juveniles is robust and is similar to adult maternal behavior.

7 tagonize progesterone's inhibitory effect on maternal behavior.

8 ne (DEX); or (2) reinstating some aspects of maternal behavior.

9 0 mg/kg), there were significant deficits in maternal behavior.

10 vironmental differences or by differences in maternal behavior.

11 rocesses, including emotional reactivity and maternal behavior.

12 R delta subunit (delta(0/0)) exhibit altered maternal behavior.

13 minantly indirect and mediated by changes in maternal behavior.

14 enetic make-up of the pups on the outcome of maternal behavior.

15 rain areas not traditionally associated with maternal behavior.

16 njection) in the VTA on the rate of onset of maternal behavior.

17 MPOA was capable of stimulating the onset of maternal behavior.

18 social conditions can alter the patterns of maternal behavior.

19 ive female rats would stimulate the onset of maternal behavior.

20 moregulation, reward seeking, addiction, and maternal behavior.

21 e dopaminergic afferents and are involved in maternal behavior.

22 survival, female reproductive function, and maternal behavior.

23 tly affect infant abuse or other measures of maternal behavior.

24 Mest is associated with embryonic growth and maternal behavior.

25 onal processes underlying the performance of maternal behavior.

26 ent female mice from manifesting spontaneous maternal behaviors.

27 rtile, but mutant females exhibit inadequate maternal behaviors.

28 nd naturally rewarding behaviors: sexual and maternal behaviors.

29 partum females and support the onset of some maternal behaviors.

30 rFB/FB females appear to have largely normal maternal behaviors.

31 insights into the neural circuits regulating maternal behaviors.

32 facilitated nursing but did not affect oral maternal behaviors.

33 e POA, is important for regulating different maternal behaviors.

34 inhibited maternal aggression but not other maternal behaviors.

35 gen/progesterone administration, pups elicit maternal behavior accompanied by a robust dopamine (DA)

36 Maternal behavior, activity, and oromotor carrying capab

37 Juvenile rats can exhibit maternal behavior after being exposed continuously to ra

38 These results suggest that the impaired maternal behavior after BSTv infusion of yohimbine or id

39 This pattern of impaired maternal behavior after cocaine injection, followed by n

40 xytocin-deficient females demonstrate normal maternal behavior, all offspring die shortly after birth

41 atment with either of the variants increased maternal behavior and also promoted unusual paternal car

42 r both mother and infant, helping to promote maternal behavior and bonding.

43 ffects of prolactin include the induction of maternal behavior and increased food intake.

44 nism, suggesting a powerful influence of the maternal behavior and presence on circuit development.

45 icrog morphine shortened the latency to show maternal behavior and that 0.0 microg and 0.01 microg mo

46 Even after accounting for these maternal behaviors and traits, the selected vaginal bact

47 cleus accumbens (NA) on latency to show full maternal behavior, and Experiment 3 determined the effec

48 ors in female rats, namely, sexual behavior, maternal behavior, and postpartum sexual behavior.

49 ncy, when the neural mechanisms that support maternal behavior are being read, alter some fundamental

50 Significantly, these changes in maternal behavior are correlated with the general levels

51 tal effects of increased CRF-R activation on maternal behavior are mediated via CRF-R2 and, to a less

52 The effects of VTA baclofen on maternal behavior are similar to the effects of interfer

53 oles as primary hormones in reproductive and maternal behavior, are now being studied as neuroprotect

54 ivity in the VTA disrupts the rapid onset of maternal behavior at parturition.

55 terone is presumably exerting its effects on maternal behavior at this time) when compared to either

56 ends to the nonhormonally dependent onset of maternal behavior, but they also indicate a more limited

57 that pregnancy hormones promote the onset of maternal behavior by reducing the behavioral influence o

58 erm improvement in adult offspring; and (ii) maternal behavior can attenuate or potentiate these effe

59 Maternal behavior can be triggered by auditory and olfac

60 n offspring after the effects of maladaptive maternal behavior, childhood maltreatment, and other co-

61 support the involvement of that receptor in maternal behavior control.

62 nd striatum, neural sites important for some maternal behaviors, could be part of this process.

63 mine (DA) receptor antagonism in NA disrupts maternal behavior, determined the type of DA receptor in

64 used on contemporaneous risk factors such as maternal behaviors, dietary factors, and immediate envir

65 This transition is accompanied by specific maternal behaviors, displayed by the mother, that ensure

66 nsible for long-lasting changes that promote maternal behavior during both development and parturitio

67 l variations in the contexts and patterns of maternal behavior during pup encounters and manual simul

68 er from in utero exposures or in response to maternal behaviors early in life.

69 dl) occurs around parturition, the time when maternal behavior emerges, and may influence its onset.

70 Maternal behavior ensures the proper development of the

71 Contingent, but not noncontingent, maternal behavior facilitates more complex and mature vo

72 luding the facilitation of birth, lactation, maternal behavior, genetic regulation of the growth of t

73 mesolimbic DA system is capable of promoting maternal behavior has not been investigated.

74 individuals in these three groups expressed maternal behavior immediately before 2-DG injection.

75 interactions to induce timely activation of maternal behaviors immediately after parturition.

76 ceptor (Oxtr) are implicated in the onset of maternal behavior in a variety of species.

77 ects in growth, coordination, fertility, and maternal behavior in addition to p gene-related hypopigm

78 icipates in the neural circuit that supports maternal behavior in an adult-like manner.

79 transmission, the neurochemistry supporting maternal behavior in humans has not been described so fa

80 activity in the VTA facilitates the onset of maternal behavior in inexperienced nonpregnant female ra

81 Maternal behavior in juveniles is robust and is similar

82 sary for the normal expression of postpartum maternal behavior in mice.

83 influence mate choice, pregnancy block, and maternal behavior in mice.

84 altrexone into the VTA disrupts the onset of maternal behavior in parturient rats.

85 Maternal behavior in postpartum rats is disrupted by inc

86 The preoptic area (POA) is critical for maternal behavior in rats but little is known about what

87 and therefore POEF) facilitated the onset of maternal behavior in rats receiving an intra-VTA microin

88 hormones which influences the occurrence of maternal behavior in rats.

89 ed nucleus of stria terminalis (VBST) during maternal behavior in rats.

90 ventral tegmental area (VTA) on the onset of maternal behavior in rats.

91 neurons, while sparing fibers of passage, on maternal behavior in rats.

92 lter some fundamental neural underpinning of maternal behavior in rats?

93 onset but not the postpartum maintenance of maternal behavior in the rat.

94 egmental area (VTA) facilitates the onset of maternal behavior in virgin female rats, and injection o

95 entral administration of oxytocin stimulates maternal behavior in virgin rats, decades of animal rese

96 cates there is a neural system that inhibits maternal behavior in virgin rats.

97 en shown to be an essential brain region for maternal behaviors in mice.

98 es actually play a role in the expression of maternal behaviors in the rats and to understand what sp

99 tanding of processes and mechanisms by which maternal behavior influences the developing human brain

100 Maternal behavior is associated with an increase in the

101 sults of this study suggest that synchronous maternal behavior is associated with increased dopamine

102 here progesterone might exert its effects on maternal behavior is discussed.

103 In lactating mammals, maternal behavior is impaired by stress, the physiologic

104 Since maternal behavior is the mammalian infant's major source

105 ctions of either drug into the VTA disrupted maternal behavior, it is likely that they did so through

106 for mammalian adult pair-bond formation and maternal behavior, its function in infant social behavio

107 have special relevance for the mediation of maternal behavior, lactation, sexual behavior, and feedi

108 t, GABA-mediated inhibition was used to test maternal behavior latencies and durations of maternal an

109 mically inactivate the mPFC during tests for maternal behavior latencies.

110 Maternal behavior latency was determined by the first of

111 t engage in stable individual differences in maternal behavior (Low, Mid, High) requires assessment a

112 The link between impaired maternal behavior (MB) and cocaine treatment could resul

113 ic area (MPOA) are necessary for pup-induced maternal behavior (MB) in juvenile and adult rats, subje

114 he rat brain neural circuit known to mediate maternal behavior (MB).

115 t mice also displayed normal species-typical maternal behaviors (nesting, nursing, and pup retrieval)

116 t time that some of the natural variation in maternal behavior observed in rhesus macaque populations

117 rebrain neuronal populations involved in the maternal behavior of 27-day-old juvenile rats compared w

118 t egg dumpers can be social parasites of the maternal behavior of egg recipients, dumping is more lik

119 Maternal behavior of Mbd2-/- mice is however defective a

120 In the current study, we assessed maternal behavior of postpartum OxtrFB/FB females toward

121 n to nondetectable levels, showed the normal maternal behavior of saline-injected controls.

122 Profound deficiency is observed in maternal behavior of stathmin(-/-) females: they lack mo

123 OxtrFB/FB females toward their own pups and maternal behavior of virgin Oxtr-/- females toward foste

124 It was concluded that cocaine impairs maternal behavior only when circulating and does not hav

125 Alternatively, does cocaine alter maternal behavior only when circulating?

126 ation of the MPOA, and presumably facilitate maternal-behavior onset.

127 wasting in infants < 6 mo of age were either maternal behaviors or child biological characteristics u

128 d maternal aggression without altering other maternal behaviors or light-dark box performance, sugges

129 nt of male sexual behavior, male aggression, maternal behavior, or female sexual behavior.

130 We studied maternal behavior over the course of a year among free-r

131 l preoptic area (MPOA) is also important for maternal behavior, receives DA input, and expresses DA r

132 d(-/-)) exhibit depression-like and abnormal maternal behaviors, resulting in reduced pup survival.

133 ea-hypothalamus and is positioned to support maternal behavior since this form is regulated across pr

134 vior, including social recognition behavior, maternal behavior, social bonding, communication, and ag

135 Centrally released oxytocin regulates maternal behavior, social memory, and social bonding.

136 ing gestation or on day 7 postpartum, active maternal behaviors, such as retrieval and licking of pup

137 plicated in the emergence and maintenance of maternal behavior that forms the basis of the mother-inf

138 rdation, as well as a striking impairment of maternal behavior that frequently resulted in death of t

139 nsights into the temporal characteristics of maternal behavior that have methodological implications

140 ydnidae), exhibits relatively well-developed maternal behavior that includes guarding eggs and provis

141 ed network of female mouse brain regions for maternal behaviors that are especially enriched for oxyt

142 Because MPOA/vBST neurons are essential for maternal behavior, the results suggest that c-Fos and Fo

143 ptic area (MPOA) is known to be critical for maternal behavior, the specific role of prolactin in thi

144 In Experiment 1, the latency to show maternal behavior toward foster rat pups (sensitization

145 This study investigates 2 patterns of maternal behavior typical of mammals, using a heteropter

146 ating effect of intra-VTA MS on the onset of maternal behavior was blocked by pretreatment with naltr

147 A deficit in maternal behavior was confirmed by the lack of pup retri

148 ns in selected sites in female rats in which maternal behavior was elicited by natural parturition, s

149 To further understand CRF2's role in maternal behavior, we crossed the knockout mice with a l

150 ing pup encounters and manual simulations of maternal behavior, we have identified several specific m

151 role of the Lhb in the nonhormonal onset of maternal behavior, we used the sensitization model in wh

152 RSA and maternal behavior were dynamically interrelated over tim

153 We found that high levels of overall maternal behavior were linked with a higher likelihood o

154 e-to-face interaction with their infant, and maternal behaviors were coded by trained researchers una

155 ng postnatal development triggers changes in maternal behavior which in turn trigger long-term physio

156 /-) females show defects in reproduction and maternal behavior, with pups of TR4(-/-) dams dying soon