Early developmental and temporal characteristics of stress-induced secretion of pituitary-adrenal hormones in prenatally stressed rat pups

1991 ◽  
Vol 558 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Lorey K. Takahashi ◽  
Ned H. Kalin
2009 ◽  
Vol 40 (2) ◽  
pp. 179-184 ◽  
Author(s):  
V. A. Mikhailenko ◽  
I. P. Butkevich ◽  
E. A. Vershinina ◽  
P. O. Semenov
Keyword(s):  
Rat Pups ◽  

2014 ◽  
Vol 5 (1) ◽  
pp. 90-96
Author(s):  
Irina Pavlovna Butkevich ◽  
Tatyana Nikolayevna Shimarayeva ◽  
Viktor Anatolyevich Mikhaylenko

Previously we revealed for the first time pain response exacerbation caused by inflammation in rats born to dams exposed to stress during pregnancy (prenatal stress). The present study is devoted to tinvestigation of prenatal stress effects on psychoemotional and tonic pain reactions in rat pups during the individual development period that is characterized with a dramatic reduction of the brain serotonin level. Effects of maternal buspirone before stress during pregnancy on functional indices of psychoemotional and tonic pain systems in the offspring were also investigated. Prenatal stress increased the number of pain patterns (flexing + shaking) during different phases of the time-course of formalin-induced pain in females and males to a greater extent in males. Prenatlly stressed rat pups of both sexes failed to show reliable changes in the index of psychoemotional behavior in the forced swim test. With the aim to decrease pain response exacerbation found in prenatally stressed offspring, pregnant dams were exposed to chronic injections of serotoninergic anxiolytic and antidepressant buspirone which is an agonist of 5-HT1A receptors; prenatal effect of buspirone on psychoemotional behavior in prenatally stressed rat pups was also evaluated. Maternal buspirone normalized pain behavior and decreased considerably the time of immobility, the index of depressive behavior in the forced swim test. The present results indicate analgesic and antidepressive effects of maternal buspirone in prenatally stressed 10-day old rat pups and demonstrate sexual dimorphism in effects of prenatal stress on the time-course of formalin-induced pain. Differences in effects of prenatal influences on pain respone during the interphase in males and females indicate earlier maturation of the descending serotonergic inhibitory system of afferent pain signals modulation in males than in females and demonstrate that 5-HT1A receptors are involved in this process.


2017 ◽  
Vol 11 ◽  
pp. 117906951770466 ◽  
Author(s):  
Nombuso Valencia Pearl Mkhize ◽  
Lihle Qulu ◽  
Musa Vuyisile Mabandla

Febrile seizures are childhood convulsions resulting from an infection that leads to an inflammatory response and subsequent convulsions. Prenatal stress has been shown to heighten the progression and intensity of febrile seizures. Current medications are costly and have adverse effects associated with prolonged use. Quercetin flavonoid exhibits anti-inflammatory, anti-convulsant, and anti-stress effects. This study was aimed to investigate the therapeutic effect of quercetin in a prenatally stressed rat model of febrile seizures. We hypothesized that quercetin will alleviate the effects of prenatal stress in a febrile seizure rat model. On gestational day 13, Sprague-Dawley rat dams were subjected to restraint stress for 1 hour/d for 7 days. Febrile seizures were induced on postnatal day 14 on rat pups by intraperitoneally injecting lipopolysaccharide followed by kainic acid and quercetin on seizure onset. Hippocampal tissue was harvested to profile cytokine concentrations. Our results show that quercetin suppresses prenatal stress–induced pro-inflammatory marker (interleukin 1 beta) levels, subsequently attenuating febrile seizures. This shows that quercetin can be therapeutic for febrile seizures in prenatally stressed individuals.


1990 ◽  
Vol 47 (2) ◽  
pp. 357-364 ◽  
Author(s):  
Lorey K. Takahashi ◽  
Eric W. Baker ◽  
Ned H. Kalin

Behaviour ◽  
1980 ◽  
Vol 75 (1-2) ◽  
pp. 82-95 ◽  
Author(s):  
Benjamin D. Sachs ◽  
Gail Richmond

AbstractIn two experiments detailed observations and quantitative analyses were made of the development and adult expression of grooming in laboratory rats. In the first experiment, 5 litters of rat pups were observed each day from 0-28 days of age, and grooming movements were recorded on paper. Forepaw wipes of the nose appeared by Day 3, followed by eye wipes (Day 6) and ear wipes (Day 8). These movements were integrated into normal-appearing head grooming on Day 11. The mouth was used to groom posterior portions of the body beginning on Day 14 with the belly, and continuing subsequently with hip (Day 15), back (Day 18), and the anogenital region and tail (Day 20). Thus, these aspects of grooming followed a general cephalocaudal progression. In contrast, the development of scratching of the head and body, which began on Day 6, did not follow a systematic order. In the second experiment, 5 adult male rats were observed in glass aquaria, which also served as their living compartments, and bouts of grooming were recorded on videotape for later analysis. Sequential and spatial characteristics of movements were determined by replaying the videotapes in slow motion, while temporal characteristics were determined by a frame-by-frarne analysis of the tapes. This experiment revealed a cephalocaudal progression of acts within bouts of grooming: grooming usually began with the paw-lick- nose-wipe sequence and progressed from there to eye wipes and ear wipes. Mouthing of the torso followed, usually beginning with more anterior portions and terminating with more posterior portions. Scratching with the hindpaws was unpredictably interpolated into the grooming sequence. The experiment also revealed that transitions between grooming different parts of the body were predictable from the spatial and temporal characteristics of the grooming. That is, the last stroke in chains of nose, eye, or ear wipes was reliably slower than previous strokes in the chain, and also tended to be incomplete. Thus, the order in which grooming of specific body areas emerges during early development follows an anterior-posterior progression, and this progression closely parallels the sequence in which body areas are groomed by adult rats. Furthermore, in adults these movements obey specific temporal and spatial rules which can be used to predict transitions of grooming from one body area to the next. This parallel between the ontogenetic and adult expressions of grooming may reflect, respectively, the maturation and activation of genotypically determined, functional units in the central nervous system. In addition, theories now being applied to the problem of transitions between different motive systems (e.g., eating and drinking), may be extended to account for transitions within a motive system (e.g., from grooming of one part of the body to the next).


Author(s):  
Vivette Glover ◽  
Thomas G. O’Connor

I (V.G.) first got to know Channi at the inaugural Indian Biological Psychiatry meeting In Bombay over 20 years ago. I was working on monoamine oxidase at the time. It was my first trip to India and his first to Bombay for several decades. We spent much time talking together, and by the end of it, as well as visiting temples, the Gateway of India, and the Elephanta Caves. Channi had persuaded me to carry out research on maternal mood in the perinatal period, the effects on the child, and the underlying biological mechanisms. This I have been doing ever since. Thus for me, like many others, Channi changed the direction of my career. His infectious enthusiasm, and very wide range of interests, have directed and inspired world research in perinatal psychiatry. There is now considerable evidence from both human and animal studies that the children of stressed, anxious, or depressed mothers are more likely to experience a range of neurodevelopmental problems than the children of unstressed mothers. (Glover 2011; O’Donnell et al. 2009; Talge et al. 2007; Van den Bergh et al. 2007,). With animal studies it is much easier to establish that these associations are causal. Newborn rat pups of prenatally stressed mothers can be cross-fostered to non-stressed mothers on the first day after birth, with control pups of unstressed mothers cross-fostered also. This can establish that any differences in outcome are caused by stress in the prenatal period. Many such studies have shown that there are definite fetal programming effects of prenatal stress on behaviour, cognitive development, the hypothalamuspituitaryadrenal (HPA) axis, and brain structure and function of the offspring (e.g. Henry et al. 1994; Weinstock 2001, 2008; Afadlal et al. 2010). The nature of the effects can be affected by the timing of the exposure in gestation, the type of the stress, the strain of the animal, the age at which the offspring was tested, and the sex of the offspring (Weinstock 2008), The effects of prenatal stress on the offspring can often be mimicked by giving the stress hormone corticosterone, or a synthetic glucocorticoid, to the pregnant animal (Matthews 2000; Afadlal et al. 2009).


Author(s):  
J. P. Revel

Movement of individual cells or of cell sheets and complex patterns of folding play a prominent role in the early developmental stages of the embryo. Our understanding of these processes is based on three- dimensional reconstructions laboriously prepared from serial sections, and from autoradiographic and other studies. Many concepts have also evolved from extrapolation of investigations of cell movement carried out in vitro. The scanning electron microscope now allows us to examine some of these events in situ. It is possible to prepare dissections of embryos and even of tissues of adult animals which reveal existing relationships between various structures more readily than used to be possible vithout an SEM.


Author(s):  
V. Kriho ◽  
H.-Y. Yang ◽  
C.-M. Lue ◽  
N. Lieska ◽  
G. D. Pappas

Radial glia have been classically defined as those early glial cells that radially span their thin processes from the ventricular to the pial surfaces in the developing central nervous system. These radial glia constitute a transient cell population, disappearing, for the most part, by the end of the period of neuronal migration. Traditionally, it has been difficult to definitively identify these cells because the principal criteria available were morphologic only.Using immunofluorescence microscopy, we have previously defined a phenotype for radial glia in rat spinal cord based upon the sequential expression of vimentin, glial fibrillary acidic protein and an intermediate filament-associated protein, IFAP-70/280kD. We report here the application of another intermediate filament-associated protein, IFAP-300kD, originally identified in BHK-21 cells, to the immunofluorescence study of radial glia in the developing rat spinal cord.Results showed that IFAP-300kD appeared very early in rat spinal cord development. In fact by embryonic day 13, IFAP-300kD immunoreactivity was already at its peak and was observed in most of the radial glia which span the spinal cord from the ventricular to the subpial surfaces (Fig. 1). Interestingly, from this time, IFAP-300kD immunoreactivity diminished rapidly in a dorsal to ventral manner, so that by embryonic day 16 it was detectable only in the maturing macroglial cells in the marginal zone of the spinal cord and the dorsal median septum (Fig. 2). By birth, the spinal cord was essentially immuno-negative for this IFAP. Thus, IFAP-300kD appears to be another differentiation marker available for future studies of gliogenesis, especially for the early stages of radial glia differentiation.


1995 ◽  
Vol 38 (5) ◽  
pp. 1014-1024 ◽  
Author(s):  
Robert L. Whitehead ◽  
Nicholas Schiavetti ◽  
Brenda H. Whitehead ◽  
Dale Evan Metz

The purpose of this investigation was twofold: (a) to determine if there are changes in specific temporal characteristics of speech that occur during simultaneous communication, and (b) to determine if known temporal rules of spoken English are disrupted during simultaneous communication. Ten speakers uttered sentences consisting of a carrier phrase and experimental CVC words under conditions of: (a) speech, (b) speech combined with signed English, and (c) speech combined with signed English for every word except the CVC word that was fingerspelled. The temporal features investigated included: (a) sentence duration, (b) experimental CVC word duration, (c) vowel duration in experimental CVC words, (d) pause duration before and after experimental CVC words, and (e) consonantal effects on vowel duration. Results indicated that for all durational measures, the speech/sign/fingerspelling condition was longest, followed by the speech/sign condition, with the speech condition being shortest. It was also found that for all three speaking conditions, vowels were longer in duration when preceding voiced consonants than vowels preceding their voiceless cognates, and that a low vowel was longer in duration than a high vowel. These findings indicate that speakers consistently reduced their rate of speech when using simultaneous communication, but did not violate these specific temporal rules of English important for consonant and vowel perception.


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