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1 imals infected in diestrus I or diestrus II (proestrous and estrous animals had less than 20% of infe
2 ed DA neuron population activity only during proestrous and estrous stages.
3  system can be considered more active during proestrous and following OVX since the output of luteini
4 alpha, 5alpha-THP in the PRF were greater in proestrous and hormone-primed rats, that are typically m
5 voked nocifensive behavior in female rats at proestrous and in OVX rats after E2 treatment.
6              In contrast, female rats in the proestrous and oestrous stages exhibited reduced sensiti
7  of noradrenaline, and also in anaesthetised proestrous and ovariectomised rats following electrical
8 ccording to estrous stage (proestrous or non-proestrous) at the time of surgery.
9 VP exerted the same effects on diestrous and proestrous days of the ovarian cycle, whether hours befo
10                           Regularly cycling, proestrous female rats received infusions of 200 ng of t
11 o cardiosomatic stimulation between male and proestrous female rats, despite differences in estradiol
12 rats, but this effect was most evident among proestrous female rats, which had the poorest spatial pe
13 ation in pentobarbital-anesthetized male and proestrous female rats.
14 naptic measures in gonadally intact male and proestrous female rats.
15                                              Proestrous females exhibited LF-LTP but males did not, s
16                                              Proestrous females had the highest microdialysate concen
17 ore DOR-labeled spines of pyramidal cells in proestrous females than males.
18 d, ovariectomized rats, lordosis behavior of proestrous females was less affected by VMN infusions wi
19                        NTI blocked LF-LTP in proestrous females, but CTOP did not.
20 ncreased postsynaptic DORs mediate LF-LTP in proestrous females.
21 nal autoreceptor may exert a greater role in proestrous females; the serotonin transporter appears to
22 ls for metestrous (low estrogen) but not the proestrous (high estrogen) group.
23 es from ovariectomized (OVX), diestrous, and proestrous kisspeptin-GFP mice.
24                                              Proestrous levels of 3alpha-OH-THP reversed the deficits
25 s was also evident when measuring successive proestrous luteinizing hormone surges.
26          A large proportion of GnRH cells in proestrous mice and very few GnRH cells in male mice exh
27 ippocampus-dependent spatial memory in early-proestrous mice, characterized by high levels of estradi
28  in GnRH cells is more pronounced in OVX and proestrous mice, the expression of galanin-IR in GnRH ce
29 d was increased across OVX --> diestrous --> proestrous mice.
30 rague Dawley rats that were nonpregnant (NP, proestrous), mid-pregnant (MP, days 9-10), late-pregnant
31        When slices were made from females on proestrous morning, when serum levels of 17beta-estradio
32 les were grouped according to estrous stage (proestrous or non-proestrous) at the time of surgery.
33 on ovarian RNAs from mice in diestrous (DE), proestrous (PE), and estrous (E) and identified estrous
34  with kinetic modeling in female rats in the proestrous phase and after ovariectomy and in male rats.
35 he diestrous phase of the estrous cycle, the proestrous phase, and after ovariectomy.
36 n rats after ovariectomy than in rats in the proestrous phase.
37  just before (ZT10) the expected time of the proestrous preovulatory luteinizing hormone surge.
38 cysts and healthy uterus were harvested from proestrous rats and immunostained using the pan-neuronal
39 anserin and ketanserin, were investigated in proestrous rats and in ovariectomized rats hormonally pr
40  phase interacted with temperature such that proestrous rats performed better overall under the warm
41                            In anaesthetised, proestrous rats receiving electrical stimulation no sign
42                                              Proestrous rats receiving intromissions (mated group) fr
43                                 In contrast, proestrous rats showed the largest response to methiothe
44                                              Proestrous rats were infused intraventricularly with eit
45                                   A group of proestrous rats were treated with phenoxybenzamine at do
46                           Sexually receptive proestrous rats with bilateral cannulae in the ventromed
47 er, OFQ failed to produce antinociception in proestrous rats, the phase of the estrous cycle with the
48 re localized by immunoelectron microscopy in proestrous rats.
49 smaller responses were seen in diestrous and proestrous rats.
50  secretion, because alcohol also blocked the proestrous surge in adrenalectomized females.
51 tral reproductive endocrine event; i.e., the proestrous surge of gonadotropins, which triggers ovulat
52           Alcohol administration blocked the proestrous surge of LH and ovulation.
53  neurons had been active during the previous proestrous surge.
54  the magnitude of the decline was smaller in proestrous than in hormone-primed, ovariectomized rats.
55  vastly more prevalent in the spinal cord of proestrous vs. diestrous females and vs. males.