1 T in males than in females during estrous or
diestrous.
2 g) increased hypothalamic 5-HT in males, and
diestrous and estrous females to approximately 2 pg/samp
3 ly more resistant to seizure-induction, than
diestrous and males rats.
4 In
diestrous and metestrous rat bladders, ERalpha was not a
5 mented differences in sleep patterns between
diestrous and pregnant rats, reproductive state did not
6 AVP exerted the same effects on
diestrous and proestrous days of the ovarian cycle, whet
7 oxetine while smaller responses were seen in
diestrous and proestrous rats.
8 n in brain slices from ovariectomized (OVX),
diestrous,
and proestrous kisspeptin-GFP mice.
9 e show that blocking glutamate signalling in
diestrous animals inhibits LH pulses, and that optic sti
10 roductive tract-draining LN from estrous and
diestrous animals.
11 ver was about 2-fold greater in male than in
diestrous day one (D(1)) female rats in the diagonal ban
12 NA-Seq analysis on ovarian RNAs from mice in
diestrous (
DE), proestrous (PE), and estrous (E) and ide
13 The authors exposed estrous or
diestrous female hamsters (Mesocricetus auratus) to sali
14 In
diestrous female mice, only 20-Hz activation generated s
15 Levels in
diestrous females (0.98 +/- 0.09 pg, n=38) were not sign
16 evalent in the spinal cord of proestrous vs.
diestrous females and vs. males.
17 Diestrous females had the highest levels during the dark
18 However, gonadally intact males, but not
diestrous females, were able to discriminate object loca
19 No such difference was observed in
diestrous females.
20 posterior MeA was higher in estrous than in
diestrous females.
21 rized resting membrane potential compared to
diestrous females.
22 They found that estrous (but not
diestrous)
females investigated conspecific male odors l
23 arizing sag and was increased across OVX -->
diestrous --&
gt; proestrous mice.
24 aled that AVP increased [Ca(2+)]i in >80% of
diestrous kisspeptin neurons via a mechanism involving v
25 le-aged (MA, 400-430 d) and young (Y, 70 d),
diestrous mice, respectively.
26 secretion in estrous mice but inhibits it in
diestrous mice.
27 ochemically identified supraoptic neurons of
diestrous or lactating female rats.
28 rmine (18)F-FES uptake in female rats in the
diestrous phase of the estrous cycle, the proestrous pha
29 nd mammary glands but was highest during the
diestrous phase of the estrous cycle.
30 er during the estrous (estrogen dominant) or
diestrous (
progesterone dominant) stage of the estrous c
31 of immunoreactive FOS in early pregnant and
diestrous rats in the medial septum (MS), vertical and h
32 on of OFQ in male, ovariectomized (OVX), and
diestrous rats produced a significant antinociceptive ef
33 ent, older, persistent estrous or persistent
diestrous rats were infected by kidney injection and giv
34 e BSTv did not differ between postpartum and
diestrous rats, but serotonin turnover was lower in moth
35 virus per gram of tissue than the persistent
diestrous rats.
36 ediate early gene expression between OVX and
diestrous rats.
37 n anxiety-related behaviors in postpartum or
diestrous rats.
38 Female rats showed
diestrous smears during the first week of treatment and
39 is less effective when initiated during the
diestrous stage compared with during the estrous stage.
40 ificantly increased in algorithm-identified '
diestrous stage' PNA mice compared to controls.
41 ignificantly greater in male rats and during
diestrous than during estrous.
42 Postpartum rats are less anxious than
diestrous virgin females, a phenomenon requiring that mo
43 Groups of
diestrous virgins were also examined.
44 ut had no effect on the open-arm behavior of
diestrous virgins.