Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “FOWLS”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 595 records · Page 33Linked to original sources

An ultrastructural study of periderm granules in the regenerating feather of the jungle fowl.

Periderm granules in the support cells of regenerating feathers of mature male Jungle Fowls were studied ultrastructurally and histochemically. Histochemical results showed the absence of carbohydrate and lipid, and the presence of protein in the periderm granules. The periderm granules were measured at successive levels of feather regeneration. The mean size of the periderm granules increased significantly as the regenerating feather matured, and this observation was suggestive of a storage function, perhaps of surplus of waste protein. The cells in which the periderm granules are found also contain glycogen. There are numerous desmosomal junctions on their interdigitating plasma membranes. These transient cells may collect waste, provide nutrition, and serve as a protective barrier for the definitive cells of the regenerating feather.

Animals↗

Calbindin immunoreactivity in the neurons of the spinal cord and dorsal root ganglion of the domestic fowl.

The distribution of the vitamin D-dependent calcium-binding protein, calbindin, was mapped in the brachial spinal cord and in the 15th dorsal root ganglion of the domestic fowl, using fluorescence immunohistochemistry. Cell somata of the dorsal root ganglion ranged in area from 200 microns 2 to 2000 microns 2. Sixteen percent of cell bodies displayed calbindin immunoreactivity. Reactivity occurred in both the small and large sensory neurons. These were randomly distributed within each ganglion. In the spinal cord, calbindin immunoreactivity was intense in Lissauer's tract, and in nerve fibres and nerve cell bodies within laminae 1 to 3 of the dorsal horn. Scattered varicose fibres were observed in laminae 4 to 7. Immunoreactivity was intense in laminae 10 where nerve fibers formed a meshwork around the central canal. Immunoreactive perikarya were occasionally observed in the outer region of lamina 10 and between laminae 8 and 9. The perikarya of the large motoneurons of lamina 9 were not reactive although they were enmeshed in calbindin-immunoreactive fibres.

Animals↗

The preoptic area of the domestic fowl. I. A Golgi study.

The preoptic area of the domestic fowl (Gallus gallus) was studied by means of the Golgi technique. At least two regions can be recognized: (i) a medial and (ii) a lateral area, clearly distinguishable laterally from the adjacent telencephalic regions. The dendritic organization of the preoptic area is quite uniform. The neurons can be classified as isodendritic elements. The magnocellular elements are few and irregularly scattered mostly in the periventricular grey of the medial preoptic area. Of relevant interest is also the observation of some bipolar and horizontal neurons in the dorsal part of the medial preoptic area, near the anterior commissure.

Animals↗

The preoptic area of the domestic fowl. II. Ultrastructure of the medial preoptic area.

Numerous secretory parvocellular perikarya were found in the preoptic region of the domestic fowl (Gallus gallus). The dense-core secretory vesicles belong to two categories: vesicles with a diameter of (i)80-90 nm and (ii) 110-140 nm. Scattered magnocellular elements display larger dense-core granules. The parvocellular neurons form unit-like clusters, showing also zones of direct apposition of neuronal membranes. The surrounding neuropil is rich in synaptic structures, formed by at least three types of axon terminals, distinguishable on the basis of vesicular morphology. These observations confirm the findings in other avian species. The hypothetical function of this system of peptidergic neurons in the rostral hypothalamus of birds is discussed.

Animals↗

The fine structure of the vesicular component of the ultimobranchial gland of the domestic fowl.

The ultrastructure of the polymorphic vesicular component of the ultimobranchial gland of the domestic fowl (Gallus gallus domesticus) has been described in detail, together with the structure of the cell strands interconnecting the vesicles and the parathyroid nodules lying within the ultimobranchial stroma. The vesicles frequently appear to arise from the nodules by way of the cell strands. The strands show a structure of their component cells intermediate between that of the parathyroid and the vesicular cells, although the position at which the strand changes from an essentially parathyroid structure to an essentially vesicular structure is very variable. The degree and kind of secretory activity within different cell types has been described. A review of the structure of ultimobranchial glands throughout the vertebrates shows that similar tissue with a similar secretory potential has been observed in all vertebrate classes, suggesting a functional significance for this part of the gland.

Animals↗

Scanning electron microscopic analysis of the linings of the fourth ventricle in the domestic fowl.

Surface features of the ependymal linings of the fourth ventricle in the fowl were analyzed employing the scanning electron microscope (SEM). On the floor of the median sulcus, each ependymal cell has a solitary cilium, whereas on both sides of the sulcus, cilia are so densely distributed that the details of the underlying cell surface are usually obscured. On the roof of the fourth ventricle, except for the surface of the ciliated groove where numerous cilia are present, the ependymal cells are polygonal in shape, and the center of each cell possesses an aggregate of ten to twenty cilia. Cell surfaces of the choroid tela are entirely covered with delicate microvilli and possess clumped cilia. The ependymal cell surfaces of the area postrema are dome-like in shape. Each ependymal cell has a solitary cilium and shows a smooth surface free of microvilli.

Animals↗

Scanning electron microscopy of the ventricular surface of the paraventricular organ in the domestic fowl.

The ventricular surface of the paraventricular organ in the domestic fowl is covered with supraependymal fiber elements. These fibers from a dense network having a web-like appearance and a coarse network of fibers running over the ventricular surface. The dense, web-like networks are mainly distributed throughout the caudal region of this organ, whereas the course networks are observed in the rostral region. In addition to these structures, spherical bodies with diameters approximately 2.5 to 6 micron are also encountered.

Animals↗

Ultrastructural alterations of the pancreatic D cell in the domestic fowl following vagotomy.

In an attempt to determine the neural control of pancreatic D cells, the pancreatic islets of the domestic fowl were examined electron microscopically from 1 to 28 days after abdominal vagotomy. Exocytotic release of many secretory granules from D cells occurred one day after vagotomy. Rough endoplasmic reticulum developed and formed an arrangement of concentric whorls in the cytoplasm of D cells after axotomy. The altered D cells were also characterized by the occurrence of many peculiar dense bodies in the apical cytoplasm at all time periods studied. These bodies varied in shape and size, containing several round vesicles. The D cells were extensively depleted of granules after the longer time periods following vagotomy. The present results provide new morphological evidence for the vagus-nerve control of D cells, which may regulate the activity of islet cells.

Animals↗

Differentiation of sympathetic and enteric neurons of the fowl embryo in grafts to the chorio-allantoic membrane.

Sympathetic cells (adrenergic neurons, SIF cells and chromaffin cells) and enteric neurons differentiate from migratory cells derived from the neural crest. The development of these cell types was studied in chorio-allantoic membrane (CAM) grafts, using combinations of tissue from domestic fowl embryos. Neural anlagen (neural tube and crest) of the vagal, cervico-thoracic and lumbo-sacral axial levels were equally capable of sympathetic differentiation, but this required somitic tissue for its significant expression. However, the vagal somites possessed only slight sympathogenic activity, thereby accounting for the negligible contribution of the vagal neural crest to the sympathetic nervous system. The same three levels of the neural anlage could furnish enteric neurons when combined directly with the aneuronal colo-rectum. However, the scale of this line of differentiation varied with the level of origin of the neural anlage, in contrast to the apparent equivalence in the ability to diffentiate as sympathetic cells. The density of enteric neurons in combinations with the vagal neural anlage was estimated as 60 times greater than the neuron density in combinations with the cervico-thoracic neural anlage. The lumbo-sacral neural anlage gave results similar to those of the cervico-thoracic level. Moreover, neural crest-derived pigment cells, positioned ectopically in the wall of the colo-rectum, were rare in combinations with the vagal neural anlage, but common in grafts with the other levels. When tested physiologically, the colo-rectum grown with the vagal neural anlage showed non-adrenergic, non-cholinergic inhibitory nervous activity in addition to the expected cholinergic excitatory responses. The neurons derived directly from vagal neural anlagen were similar to those that had reached the colo-rectum via their normal migratory pathways, when studied in terms of histological appearance, density of distribution and physiological responses.

Allantois↗

The seminiferous epithelium in the guinea fowl (Numida meleagris).

Spermiogenesis and cellular associations in the seminiferous epithelium of the guinea fowl were studied and described in "sexually" active adult birds. PAS stain was found to be useful in the recognition of steps of spermatid differentiation only in the first early stages. Nuclear morphological changes were subsequently found to be more reliable in tracing steps of spermiogenesis. It was observed that haematoxylin-eosin stained tissue can be used in the study of spermiogenesis in the bird. Various stages of the seminiferous epithelium were observed in any cross-section of the seminiferous tubules. Distinct cellular associations were observed, but intermix of adjacent germ cells or heterogenous cellular associations were frequently encountered.

Acrosome↗

A histochemical study of the innervation of the cerebral blood vessels in the domestic fowl.

Adrenergic and cholinergic nerves innervating the cerebral arteries of the domestic fowl were examined by specific histochemical techniques. The adrenergic nerve plexuses of the cerebral carotid system are markedly denser than those of other vertebrates observed by similar techniques. They form longitudinally elongated meshworks of fine fibres in the vascular wall of the arterial branches. Those innervating the vertebro-basilar system are less dense and more elongated, and, as the size of the artery diminishes, the fibres of the plexus become coarser. In the small pial and parenchymal arteries they are reduced to a few fibres running parallel to, or spiralling around the vascular axis. The cholinergic nerve plexuses are not as dense as the adrenergic system. The acetylcholinesterase activity is very weak, except in the plexuses innervating the cerebral carotid artery and proximal portion of the anterior and posterior rami. In the vertebro-basilar system, a few thick nerve bundles run alongside the blood vessels of the vertebral and basilar arteries. Cholinergic nerves enter the cranial cavity along the internal carotid, the vertebral and possibly the cerebroethmoidal arteries. Intracerebral capillaries and some arterioles are not innervated with cholinergic and adrenergic fibres of peripheral origin, but with ones arising from parenchymal nerve cells.

Adrenergic Fibers↗

Disintegration of spermatozoa in the infundibular sperm-host glands of the fowl.

The disintegration of spermatozoa in the infundibular sperm-host glands of the fowl was investigated by electron microscopy. After the 15th day following artificial insemination, secretory granules in the epithelial cells of the sperm-host glands increase in number and size, and subsequently the contents of the granules are released into the granular lumen, so that the electron density of the lumen increases. At this stage, spermatozoa stored in the glands begin to undergo degenerative changes starting from the head. The heads become distended and chromatin of the nucleus begins to disperse as small masses, simultaneously with the destruction of the acrosome. As the dispersion of chromatin progresses, mitochondria of the middle piece become distended and irregular in shape, and then disintegrate. At the last stage, most of the organelles have disappeared, but the fibrous sheath and axial-filament complex are still identified.

Animals↗

Functional organization of some auditory nuclei in the guinea fowl demonstrated by the 2-deoxyglucose technique.

The auditory pathway of the Guinea Fowl was labeled with [C14]2-deoxy-D-glucose after stimulation with pure tones, harmonic tones and species-specific calls. In addition to other auditory nuclei, which showed more or less uniform labeling with the present technique, the n. mesencephalicus lateralis dorsalis (MLD) of the midbrain, as well as field L and parts of the hyperstriatum ventrale in the telencephalon, showed a stripe-pattern of labeling after stimulation with a pure tone. The position and orientation of the tone-activated striped areas in field L, observed after stimulation with different tones, correspond to isofrequency contours obtained with microelectrode recordings. The labeling of the three congruent tonotopically organized layers of field L (L1, L2, and L3) was not uniform along the anterior-posterior axis of the field. Harmonic tones produced multiple reactive stripes each of which corresponded to the stripe characteristic of a particular harmonic presented as a pure tone. The species-specific Iambus-call labeled the tonotopic area of field L that corresponds to the frequency band with the highest energy of the call. The hyperstriatum ventrale generally showed a weaker pattern of labeling that, however, resembled the labeling in field L.

Animal Communication↗

Fine structure of the ependymal cells in the area postrema of the domestic fowl.

The ultrastructure of the ependymal cells in the area postrema of the domestic fowl was studied by scanning and transmission electron microscopy. The ependymal surface of the area postrema is covered with many furrows and ridges. These ridges consist of ependymal cells aggregated in a fan-like shape. The ependymal cell lacks clustered cilia, microvilli are few, and a long basal process extends through the parenchymal layer of the area postrema. Within the cytoplasm as well as in the basal process, a spherical body with a diameter ranging from 1.5 to 2 micron is occasionally observed.

Animals↗

Connectivity of the auditory forebrain nuclei in the guinea fowl (Numida meleagris).

Injection of tritiated leucine and proline into the nucleus ovoidalis of the Guinea Fowl (Numida meleagris) produces terminal labeling in the palaeostriatum and in three adjacent zones (field L1-L3) of the auditory neostriatum (AN). L2, situated between L1 and L3, receives the main input and corresponds to the former field L of Rose. These neuroanatomically defined zones of the auditory neostriatum are also characterized by differing properties of their neurons. Injection of radioactive material into the auditory neostriatum produces labeling of (i) a palaeostriatal, (ii) a ventral hyperstriatal, and (iii) an additional neostriatal area (Nd). Injection into the hyperstriatum ventrale reveals connections (i) to field L2, (ii) to the palaeostriatum, (iii) to Nd, and (iv) to the archistriatum. After injection into the palaeostriatum, labeling can be observed (i) in the neostriatum dorsale, (ii) in the hyperstriatum ventrale, (iii) in the archistriatum, (iv) in the diencephalic nuclei, nucleus ansae lenticularis and nucleus spiriformis lateralis, and (v) in the mesencephalic nuclei, nucleus tegmenti pedunculo-pontinus and nucleus intercollicularis. These results show that a widespread connectivity exists among primary and presumably higher order auditory areas in the forebrain of birds. Connections also exist between these auditory areas and presumed vocal-motor areas (neostriatum dorsale, archistriatum, nucleus intercollicularis).

Animals↗

Evidence for neuronal periodicity detection in the auditory system of the Guinea fowl: implications for pitch analysis in the time domain.

Evidence for periodicity analysis was obtained by recording from 420 single units in the auditory midbrain nucleus (MLD) of awake Guinea fowls (Numida meleagris). The results were compatible with a neuronal correlation model consisting of three main components: an oscillator, an interval multiplier and a coincidence unit. The model makes use of a neuronal time constant in order to measure the periodicities of auditory signals. For 180 units the sequence of spike intervals in response to tone bursts and amplitude modulations (AM) was studied with 10 microseconds resolution. In 69 of these units (38%) amplitude fluctuations like stimulus onset or the modulation cycles produced periodic spike trains resembling damped oscillations. The periods of these oscillations did not correspond to either the best frequency (BF) of these units or the periodicities of the stimuli. They were interpreted as multiples of a neuronal time constant, tau 1 = 0.4 ms, probably a minimal synaptic delay. These units were tuned to AM-signals with particular combinations of the modulation frequency, fm, and the carrier frequency, fc. The corresponding periods tau m and tau c were related to the intrinsic oscillation by a periodicity equation: m X tau m + n X tau c = 1 X tau 1, where a few small integers for m, n and 1 were adequate to describe all observed properties of a unit. Variation of fm or fc shifted the phase delays of the coupled spike activities proportional to m X tau m or n X tau c, respectively. These effects were explained by coincidence of neuronal activity phase coupled to fc, with intrinsic oscillations triggered by the fm-cycles. The coincidence condition at the level of the recorded units was given by the periodicity equation. Psychophysical experiments using AM-signals indicated that the described mechanisms, together with the same neuronal time constant, tau 1, are adequate to explain pitch perception in humans.

Animals↗

Tone-versus FM--induced patterns of excitation and suppression in the 14-C-2-deoxyglucose labeled auditory "cortex" of the guinea fowl.

The primary auditory "cortex" field L, of the Guinea fowl is a three layer tonotopically organized structure. Isofrequency planes as shown with the 2-deoxyglucose (2DG) method cut across these layers and with their second dimension extend in rostro-caudal direction. The input layer L2 exhibits "spontaneous" labeling due to high spontaneous activity of input terminals and units throughout the hearing range. The labeling is stronger locally along a rostro-caudal isofrequency contour of L2 after tone or narrow band FM stimulation. With tone stimuli the layers L1 and L3 are labeled within an isofrequency plane except for the rostral half of the field whereas frequency modulated tones do label these two layers throughout the corresponding isofrequency plane. FM stimuli in addition lead to a reduction of spontaneous labeling in frequency planes adjacent to those which are covered by the stimuli. Since these effects correlate with known inhibitory effects of such stimuli it is argued that the 2 DG method can identify the suppression of activity of neurons in suitable structures.

Animals↗

High dietary sodium chloride and body temperature in the domestic fowl and the glaucous-winged gull.

Arad and Skadhauge (1986) correlated plasma sodium to calcium ratio and body temperature in domestic fowl (Gallus domesticus) during increased dietary sodium chloride intake which increased plasma sodium concentration. During acclimation to high dietary NaCl, body temperature should increase in proportion to the increase in plasma sodium concentration, and body temperature should increase less in gulls than in chickens because salt gland secretion of NaCl by gulls should prevent elevation of plasma sodium concentration. Plasma osmolality, plasma sodium concentration, plasma concentrations of total calcium and ionized calcium, and body temperature and panting threshold were measured in domestic roosters and Glaucous-winged gulls before and after exposure to high NaCl diets. Gull body temperature (40.4 +/- 0.2 degrees C) increased significantly (P < 0.05) during salt acclimation. Rooster body temperature (41.0 +/- 0.2 degrees C) did not increase significantly. Plasma sodium concentration increased in gulls (5.4 +/- 0.5%, P < 0.01) and was correlated with body temperature (r = 0.497, P < 0.05); the 3.8 +/- 1.0% increase in plasma sodium concentration in roosters (P < 0.01) was not, suggesting that change in body temperature might be a response to the magnitude of increase in plasma sodium concentration. Plasma ionized calcium concentration increased by 12.9 +/- 4.6% (P < 0.01) in gulls and by 5.3 +/- 1.0% (P < 0.01) in roosters. Plasma sodium concentration was correlated with calcium ion concentration in both gulls (r = 0.635, P < 0.05) and roosters (r = 0.664, P < 0.05). In neither species were ratios of sodium to total calcium plasma concentration or sodium to ionized calcium concentration altered or related to body temperature.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗