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D W Pfaff

Publications and source records attributed to D W Pfaff.

At least 235 records · Page 13Linked to original sources
PubMed1989

Studies of ventromedial hypothalamic afferents in the rat using three methods of HRP application.

The afferent neural connections of the ventromedial nucleus of the rat hypothalamus (VMH) have been studied in detail using three horseradish peroxidase (HRP) application methods: HRP crystal implants, HRP-gel implants, and iontophoretic deposition of the enzyme. Examination of the cases in which the retrograde tracer was best confined to various subdivisions of the nucleus revealed that the septal area projects only to the ventrolateral VMH, and that the medial preoptic area, rostral lateral hypothalamus, and the ventral subiculum project mainly to the ventrolateral VMH. Thus, the subdivision of the VMH that contains the highest density of estradiol-concentrating neurons (Morrell et al. 1986) receives a larger set of inputs than the rostral and central parts of the nucleus. The central subdivision receives a more restricted set of projections than either the medial or the lateral regions. These studies suggest that there may be partial anatomical segregation of neural inputs to the various subdivisions of the VMH.

Afferent Pathways↗
PubMed1989

Medial preoptic islands in the rat brain: electron microscopic evidence for intrinsic synapses.

Neurons intrinsic to the preoptic area might participate in the control of neuroendocrine or behavioral events. To determine their existence and features, we deafferented the preoptic area of female rats, using completely circumscribing cuts with a Halasz knife. Despite obvious signs of degeneration of synapses originating from nerve cell bodies outside the preoptic island, some synapses survived complete deafferentation. We saw synaptic contacts not only on the neuronal cell body, but also on the dendritic shaft and spine. There were no peculiar morphological features, as might suggest unique physiologic functions of these intrinsic synapses. The prominence of intrinsic synapses in the preoptic area suggests that, in addition to hormone effects on preoptic neurons, and long ascending afferents, intrinsic synapses might play significant roles in neuroendocrine controls.

Animals↗
PubMed1989

Longer term progesterone treatment induces changes of GABAA receptor levels in forebrain sites in the female hamster: quantitative autoradiography study.

Quantitative receptor autoradiography was applied to evaluate the effects of one and three injections of 1 mg progesterone (P) on 3H muscimol binding levels in the different forebrain areas of the female hamster. The overall effect of P resulted in substantial increases in 3H muscimol binding in brain areas containing gonadal steroid receptors: medial preoptic area and ventromedial hypothalamic nucleus as well as in bed nucleus stria terminalis and subiculum. Similarly, the caudate putamen, a region where gonadal steroid receptors are not abundant, also showed substantial increases of 3H muscimol binding receptor levels. Moreover, female hamsters treated with P for 3 days presented altered 3H muscimol binding levels in the amygdala and thalamic nucleus that were, in some cases, not produced by one dose of P. P treatment also decreased GABAA binding in two areas of the thalamus. These results are consistent with the proposal that P may alter GABAergic inhibitory activity via changes in the levels of GABAA receptors in certain forebrain areas in the female hamster, changes which may be linked to the mediation of anxiolytic effects and to the inhibition of aggressive behavior. These data also suggest that P treatment increases the binding of high affinity GABA receptors in some forebrain sites and may be responsible for maintenance of the anxiolytic effects.

Animals↗
PubMed1989

Patterns of steroid hormone effects on electrical and molecular events in hypothalamic neurons.

Hypothalamic neurons with nuclear receptors for steroid hormones provide opportunities to relate individual biosynthetic and electrical changes to hormone-driven behaviors. Successful work with female rodent reproductive behavior has proven that it is possible to define a neural circuit for a vertebrate behavior. In contrast to what might be expected from an invertebrate system, results from several approaches to neuronal gene expression show the complexity of hypothalamic control, even over this simple mammalian behavior. This is not a 1 hormone-1 gene-1 behavior system. Neither is there just one mode of hormonal induction. Certain steroid hormone effects can multiply each other, showing how a clear endocrine signal could be discerned among other variations in neural activity.

Animals↗
PubMed1989

Temporal actions of 16 alpha-hydroxyestrone in the rat: comparisons of lordosis dynamics with other estrogen metabolites and between sexes.

16 alpha-Hydroxyesterone (16OHE1), a metabolite of estradiol (E2) and precursor of estriol (E3), binds to the estrogen receptor (ER) with low affinity (3% of E2), but is estrogenic in both in vitro and in vivo systems. This metabolite is able to bind in a non-dissociable manner to the ER. We examined these properties in vivo by assessing the temporal dynamics of estrogen metabolite action in the rat brain, using lordosis score (LS) to manual stimulation as a serial bioassay of estrogen effect. Male and female castrate Fisher rats were implanted with osmotic minipumps containing either vehicle, E2, 16OHE1, or E3. 16OHE1-induced LS was delayed in onset in both sexes relative to E2 and E3. Male LS reached a similar plateau for all metabolites, whereas female LS reached an initial LS plateau similar in amplitude to the male plateau. Over the next several days, female LS increased to reach a secondary plateau of higher amplitude, which persisted until pump removal. Upon pump removal, E2- and E3-stimulated LS fell to baseline quickly in both sexes, whereas 16OHE1-stimulated LS in males demonstrated a prolongation of maximal LS for 6 days following pump removal. These results suggest that 16OHE1 is estrogenic in the brains of both sexes. The delay of onset of LS with 16OHE1 is consistent with its poor ER affinity. Females were able to augment LS with prolonged exposure to all metabolites, while males could not. The ability of 16OHE1 to maintain maximal LS in the male long after its withdrawal is consistent with its ability to bind non-dissociably to the ER and promote prolonged estrogenic activation. However, females do not exhibit this response, suggesting a sex specificity in the dynamics of ligand-receptor action in the rat brain.

Animals↗
PubMed1989

Responses of hypothalamic paraventricular neurons in vitro to norepinephrine and other feeding-relevant agents.

To investigate paraventricular hypothalamic neuronal actions responsible for the effects of neurotransmitters on feeding, and to test the notion that a single population of cells there could account for feeding effects, hypothalamic slices containing the paraventricular nucleus (PVN) were prepared from rats. Electrophysiological responses of individual PVN neurons to feeding-inducing agents norepinephrine (NE) and gamma-aminobutyric acid (GABA), and to anorexic agents serotonin (5-HT) and histamine (Hist) were examined. NE inhibited neuronal activity through alpha 2-adrenergic receptors, and excited through alpha 1-receptors. alpha 2-receptors are known to mediate the behavioral effect of NE. NE inhibited most clearly those neurons that otherwise fired continuously in this type of in vitro preparation. GABA affected the activity of 37% of the neurons tested, primarily by inhibition. The inhibitory action of GABA can be related to its feeding-inducing effect. GABA in PVN can also attenuate excitatory responses and enhance inhibitory responses to NE or 5-HT. 5-HT caused excitatory and inhibitory responses with the former action outnumbering the latter by approximately 3 to 1. Since this would result in a net excitation, it appears that 5-HT in PVN inhibits feeding mainly by exciting neuronal activity. Hist excited 72% and inhibited only 2% of PVN neurons. The excitation was blocked by H1-antagonists, which have been shown to mediate Hist effect on feeding. Comparing across neurons, the inhibitory response to NE was correlated with that to GABA, but not with any responses to 5-HT or Hist. The excitatory responses to Hist correlated with 5-HT responses.(ABSTRACT TRUNCATED AT 250 WORDS)

Adrenergic Agonists↗
PubMed1989

Graphical and statistical approaches to data analysis for in situ hybridization.

Quantification of gene expression in a morphological context is an invaluable tool for neurobiological investigation. The ability to measure the quantity of specific mRNA molecules at the level of the single neuron permits one to monitor the modulation of complex cell synthetic activity of intact neuron populations. The cells of interest can be contiguous or dispersed in functionally significant patterns throughout a broad anatomical region of the brain. The application of quantitative in situ hybridization is technically difficult and labor intensive. Nevertheless, it has great utility for investigating gene expression from a structural perspective. (1) In situ hybridization permits one to ask questions concerning the anatomical pattern of neuronal gene expression. (2) It permits analyses concerning the initiation of expression, cell location, cell type, and alterations of level of expression within a spatial and temporal context. (3) In cases where blotting methods suggest a message exists at low copy, in situ hybridization permits queries at the single-cell level. For example, in situ hybridization can determine if very few cells are expressing the gene product or if many neurons dispersed throughout a brain region exhibit low mRNA copy number/cell. Quantitative analyses also allow detailed investigation of cell response to physiologically meaningful stimulation. Our application of statistical and numerical methods is a demonstration of the utility of probabilistic models; the mixture distribution accounted for data from both labeled and unlabeled sources. In agreement with many previous investigations, grain density over an unlabeled uniform source (oxytocinergic cells) was suitably described by the Poisson distribution. The population of labeled vasopressinergic cells, however, was best described by the negative binomial distribution. Previous investigations from different fields of biology show that the negative binomial can be used to describe many biological phenomena, and this distribution was considered in at least two previous investigations to evaluate autoradiographic data which did not fit the Poisson function. From a theoretical perspective, the probabilistic relationship between beta-particle decay (a Poisson function) and the distribution of message levels among individual neurons in a cell group (gamma distribution) prompts consideration of the negative binomial. For both data sets the observed variances were larger than the mean, and the labeled portion of the data sets exhibited positive skewness.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1989

Phorbol esters and forskolin infused into midbrain central gray facilitate lordosis.

Several peptides, when infused into the MCG, facilitate lordosis in estrogen-primed female rats. Since these peptides can act through cAMP and/or protein kinase C, and these second messenger systems have been implicated in neuromodulation, this study examined if pharmacological agents which stimulate these systems would facilitate lordosis. Ovariectomized female Fisher rats were given bilateral cranial cannulae targeted to the MCG, or cortex dorsal to MCG, and allowed at least a week to recover. Forty-eight hours after injection of 1.25 micrograms estradiol benzoate (EB), 1 microliter of each of the following was infused into the MCG (n=8-12): 1) forskolin (5 micrograms/microliter 50% DMSO); 2) phorbol-20-oxo-20-deoxy-12,13-dibutyrate (PBu; 5 micrograms/microliter 50% DMSO); 3) both forskolin and PBu (2.5 micrograms of each/microliter); 4) vehicle (50% DMSO). In a separate study of identical design, 1 microliter of another phorbol ester (12-myristate 13-acetate) was infused into the MCG of EB-primed rats. Forskolin and phorbol esters each facilitated lordosis maximally at 60-90 minutes after infusion. Combining both agents also facilitated lordosis, and vehicle had no effect. These results suggest that infusing agents which stimulate cAMP and protein kinase C into the MCG can facilitate lordosis in estrogen-primed female rats.

Animals↗
PubMed1989

Considerations in the quantitative analysis of autoradiograms from 2-dimensional gels.

Two-dimensional (2-D) gel electrophoresis has been used in conjunction with autoradiography and computerized optical densitometry for quantitating specific protein synthesis. However, accurate quantitation of 2-D autoradiograms requires the prior assessment of such parameters as linearity, reciprocity, and reproducibility. The present study was performed to determine the contribution of each of these to the dissimilation of beta-emission and autoradiographic density, and of density and protein synthesis. Various aliquot volumes of a single complex protein specimen labeled with 35S-amino acids were subjected to 2-D gel electrophoresis, and these gels were serially exposed at graded intervals. The peak densities and volumes of the 111 visualized spots were used to examine the above parameters. In our computerized scanning system, the peak density is a more accurate and reproducible parameter of optical density than is spot volume. Approximately 30% of the dynamic range of peak density is non-linear; quantitation of spots above or below the linear range leads to inaccuracies in quantitation. In addition, the phenomenon of reciprocity, which states that density is directly proportional to exposure (beta-emission of 35S x time), is shown to fail as aliquot volume, or mass of 35S increases. The implications of reciprocity failure to accurate quantitation are discussed. Finally, the sources of variance in autoradiographic analysis were examined, by assessing the intra-scan, intra-gel run, and inter-gel run coefficients of variation. The results of this study show that autoradiographic densitometry is an effective method for quantitation of 2-D gels, but linearity, reciprocity, and reproducibility must be assessed prior to its experimental use. Restrictions of such use are suggested.

Animals↗
PubMed1989

Estrogen regulation of proenkephalin gene expression in the ventromedial hypothalamus of the rat: temporal qualities and synergism with progesterone.

Estrogen has been shown to increase proenkephalin (PE) mRNA levels in neurons of the ventrolateral aspect of the ventromedial hypothalamic nucleus (VL-VM). In this series of experiments, we examined the temporal qualities of this induction by determining both the latency of the estrogen-induced elevation in PE mRNA levels and the rate at which the message levels decline following removal of estrogen. In addition we have examined the effects of progesterone on PE gene expression in the VL-VM of estrogen-primed rats. The latency of the estrogen-induced elevation in PE mRNA levels was found to be relatively short: PE mRNA levels were increased 2-fold within 1 h of estrogen replacement. Following estrogen removal the levels of PE mRNA declined rapidly. Progesterone treatment attenuated this decline, prolonging the estrogen-induced elevation of PE mRNA levels. These results suggest that estrogen rapidly increases PE mRNA levels through a mechanism that probably involves alterations in both the rate of appearance and the rate of degradation of the message. Together, the short latency of the estrogen-induced elevation and the rapid rate of decay following estrogen removal indicate that PE gene expression is highly sensitive to fluctuating estrogen levels. The effect of progesterone suggests that this enkephalinergic system may be regulated by both estrogen and progesterone during the estrous cycle.

Animals↗
PubMed1989

In situ hybridization for LHRH mRNA following estrogen treatment.

Elucidation of mechanisms governing the synthesis and release of the decapeptide luteinizing hormone-releasing hormone (LHRH) in the female are central for understanding how the brain influences the ovulatory surge of luteinizing hormone and facilitates female rat mating behavior. Previous immunocytochemical results suggested that estrogen treatment might increase LHRH forebrain content, but measures of peptide content often are confounded by alterations in synthesis versus peptide processing versus release. Therefore, we have used in situ hybridization with an oligomer for the LHRH coding region to detect LHRH gene expressing cells and to study LHRH message levels in estrogen treated compared to control ovariectomized rats. Neurons expressing the gene for LHRH are in the medial preoptic area and amongst the fibers of the diagonal bands of Broca. When the numbers of neurons with detectable LHRH message levels were multiplied by the average numbers of grains per cell, to achieve a metric proportional to LHRH message content, we saw a significant stimulatory effect of seven days of estrogen treatment.

Animals↗
PubMed1989

Expression of NGF receptor in the rat forebrain detected with in situ hybridization and immunohistochemistry.

The expression of nerve growth factor (NGF) receptor mRNA and NGF receptor protein was examined in the adult rat basal forebrain using in situ hybridization and immunohistochemical techniques. NGF receptor mRNA and protein were detected within cells in the medial septum, diagonal band of Broca, and nucleus basalis of Meynert. Controls showed that the hybridization signal was not due to nonspecific binding of the probe to heterologous RNAs or other molecules. As expected, the distribution of NGF receptor mRNA-containing cells correlated nicely with the distribution of NGF receptor immunoreactive cells in each of these areas. These data extend previous work which suggests that neurons in these areas express the NGF receptor mRNA and manufacture functional NGF receptors. NGF receptor immunoreactivity was also detected in the arcuate nucleus of the hypothalamus, in the leptomeninges at the base of the brain and overlying the tectum, and within ependymal regions along the lateral walls of the cerebral ventricles. A few weakly stained neurons in the lateral hypothalamus and ventrolateral striatum were also consistently observed. In contrast, NGF receptor mRNA was not detected within any meningial, ependymal, or hypothalamic tissues using in situ hybridization. A cross-linking/immunoprecipitation assay demonstrated normal, membrane-bound NGF receptors within extracts of dorsal superior colliculus, ventromedial hypothalamic, and overlying meningial tissues, proving that the staining observed in these areas was not a non-specific artifact associated with the immunohistochemistry. The lack of hybridization in these areas may reflect levels of NGF receptor mRNA which are too low to be detected by the in situ hybridization methods being used. Alternatively, the staining may represent innervation of these areas by afferents whose cell bodies are located elsewhere, and whose terminals contain the NGF receptor protein.

Animals↗
PubMed1989

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome.

Kallmann syndrome inherited hypogonadotropic hypogonadism with anosmia, is associated with an X-chromosome deletion at Xp 22.3. In a Kallmann fetus, we have found an absence of luteinizing hormone-releasing hormone (LHRH)-expressing cells in the brain despite dense clusters of LHRH cells and fibers in the nose. LHRH-containing cells and neurites end in a tangle beneath the forebrain, within the dural layers of the meninges, on the dorsal surface of the cribriform plate of the ethmoid bone. Normal fetal brains, matched for age and sex, had LHRH cells and fibers, as expected, in the hypothalamus and preoptic area. Since LHRH-expressing cells recently were discovered to migrate from the olfactory placode into the brain, it appears that the hypogonadotropism of the Kallmann syndrome can be accounted for by a failure of LHRH cells to migrate into the brain.

Brain↗
PubMed1989

Distribution and partial characterization of immunoreactive prolactin in the rat brain.

Immunoreactive (IR) prolactin was localized immunocytochemically in cell bodies in the mediobasal hypothalamus and in fibers in many regions of the rat brain. The cell bodies were found in the arcuate nuclei and the adjacent areas ventral to the ventromedial nuclei. Fiber projections extended rostrally to and/or through the anterior hypothalamus, preoptic area, nucleus accumbens, septum, diagonal bands of Broca, caudate-putamen, frontal cortex and accessory olfactory bulb; laterally to the amygdala, especially the central nucleus and some parts of the medial nucleus; caudally to and/or through the midbrain central gray, reticular formation, parabrachial region, and several portions of the lower brain stem and spinal cord extending to sacral levels. The system appears to be essentially identical to that containing proopiomelanocortin (POMC) and its processed peptides, as shown by double immunocytochemistry. Preabsorption of the antiprolactin antiserum with either prolactin or the 16,000-dalton N-terminus of POMC eliminated immunoreactivity in the brain. Preabsorption with other POMC-derived peptides, including beta-lipotropic hormone, beta-endorphin, met-enkephalin, adrenocorticotrophic hormone (1-24), corticotropin-like intermediate lobe peptide, alpha- and gamma-melanocyte-stimulating hormones and an octapeptide region of the N-terminus of POMC bearing some homology with prolactin, did not eliminate immunoreactivity in the brain. Similarly, preabsorption with growth hormone, luteinizing hormone, follicle-stimulating hormone, motilin or fetuin did not eliminate immunoreactivity in the brain. The antiprolactin antiserum also recognized all cells in the intermediate lobe and a subset of cells in the anterior lobe of the Snell dwarf mouse pituitary. This immunoreactivity was eliminated by preabsorption of the antiserum with prolactin or with the 16,000-dalton N-terminus of POMC. These results suggest that IR prolactin in the brain may be related to the N-terminus of POMC. Additional results based on one- and two-dimensional gel electrophoresis and immunoblotting indicate that the antiprolactin antiserum used in the majority of the immunocytochemical studies recognized a number of proteins.

Animals↗
PubMed1989

A subset of neurons containing immunoreactive prolactin is a target for estrogen regulation of gene expression in rat hypothalamus.

Cells whose nuclei accumulated 3H-estradiol were identified autoradiographically in fixed, frozen sections of colchicine-treated rat hypothalamus (n = 3 animals). After autoradiogram development, these sections were subjected to immunocytochemistry using rabbit antirat prolactin antiserum and the avidin-biotinylated horseradish peroxidase method. In the hypothalamus, a substantial subset of the neurons containing immunoreactive prolactin accumulated 3H-estradiol in their nuclei: of 3, 642 immunoreactive cells examined, 1,216 had autoradiographically labeled nuclei, or about 33%. The immunoreactive prolactin neurons with autoradiographically labeled nuclei were located in the medial basal hypothalamus intermingled with immunoreactive prolactin neurons whose nuclei were not labeled autoradiographically. Since hypothalamic immunoreactive prolactin neurons have a rich and widely distributed fiber system, the present results suggest that estrogen, acting through a subset of these neurons, can modify directly the neuronal activity of several brain regions which regulate diverse aspects of the reproductive effort. Also, since immunoreactive prolactin and immunoreactive beta-endorphin exist in the same hypothalamic cell population, opioid peptides derived from pro-opiomelanocortin may mediate some effects of estrogen on the neural circuitry regulating reproduction.

Animals↗
PubMed1989

Two-dimensional gel autoradiographic analysis of the acute effects of estradiol on protein synthesis in the female rat ventromedial nucleus in vivo.

Estradiol (E2) alters protein synthetic events in the ventromedial nucleus (VMN) of the hypothalamus to promote lordotic behavior in the female rat. This study analyzed the acute changes induced by E2 in proteins synthesized in the VMN in vivo as measured by 35S incorporation into protein, two-dimensional gel electrophoresis, autoradiography, and computerized optical densitometry. Ovariectomized rats received vehicle or E2, Hamilton syringes were placed stereotaxically in the VMN bilaterally, and 0.9 mCi 35S-labeled methionine and cysteine was infused over 1 h. After 6 h, rats were killed, and VMN samples were subjected to isoelectric focusing and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Resultant gels underwent autoradiography, and the optical density of each of 240 spots was quantitated using a flat-bed laser scanner. Using a quantitation algorithm based on the linearity and reproducibility of the scanner and film, 123 spots were analyzed for changes in optical density and relative mol wt (MW) and isoelectric point (pI) induced by E2. The spot induced most prominently by E2 had a MW of 70K and a pI of 6.0, confirming previous results. Three spots were quantitatively induced by E2: 1) a 47K MW, pI 5.4 phosphoprotein (96% induction); 2) a 45K MW, pI 5.2 protein (72% induction); and 3) a 100K MW, pI 5.5 protein (82% induction). Two spots increased pI with E2: 1) a 110K MW protein increased from pI 5.4 to 5.5; and 2) a 50K MW protein increased from pI 6.3 to 6.4. Under these conditions and using a quantitative algorithm, only a small number of proteins synthesized in the VMN were induced by E2 in vivo. E2 also exerts effects on the posttranslational modification of another select group of proteins. These proteins may subserve at least part of the physiological effect of E2 in the VMN.

Animals↗
PubMed1989

Differential effects of estradiol and 16 alpha-hydroxyestrone on pituitary and preoptic estrogen receptor regulation.

16 alpha-Hydroxyestrone (16OHE1), an endogenous metabolite of estradiol (E2), binds to the estrogen receptor (ER) with low affinity, but is estrogenic in various bioassay systems. 16OHE1 binds covalently to the ER in vitro, exhibits prolonged estrogenic bioactivity in vivo, and has been implicated in several estrogen-dependent diseases. This study examined the effects of 13 days of continuous infusion of E2 or 16OHE1 on lordotic behavior, pituitary growth, and ER regulation in the cytosolic and nuclear fractions of the pituitary and preoptic area of both sexes. Finally, simultaneous pituitary nuclear exchange assays and enzyme immunoassays were performed to search for covalent 16OHE1-ER complexes in vivo. E2 induced lordosis and pituitary growth in both sexes, while 16OHE1 was only slightly less effective. While E2 treatment increased nuclear ER concentrations 2-fold vs. control values, it decreased both cytosolic and total (cytosolic plus nuclear) ER concentrations in pituitary and preoptic area by approximately 3-fold vs. control values in both sexes by exchange assay. In contrast, 16OHE1 did not decrease total pituitary ER concentrations and only minimally decreased total preoptic ER concentrations. Simultaneous exchange assay and immunoassay of pituitary nuclear extracts demonstrated proportionate increases in ER levels in female vs. male and in E2-treated vs. 16OHE1-treated rats. The ratios of (ER enzyme immunoassay divided by ER-exchange) for each rat were similar regardless of metabolite administration. The correlation of individual measurements implied that ER localized to the nuclear fraction by either E2 or 16OHE1 retained both exchangeability and immunoassayability to similar extents, but did not support the presence of 16OHE1-ER covalent complexes. The results of this study suggest that 16OHE1 has significant estrogenic bioactivity, as manifest by its effects on lordosis and pituitary growth, but, in contrast to E2, does not decrease pituitary ER concentrations and only minimally decreases preoptic ER concentrations. This property may be important in the proposed pathogenetic action of 16OHE1 in estrogen-dependent disease.

Aging↗