Subcutaneous feather tract denervation does not alter feather retention force ante- and postmortem in broilers.

To determine whether feather retention force (FRF) in 6-wk-old commercial broilers was influenced by the presence or absence of cutaneous innervation, nerve trunks for the pectoral and sternal feather tracts were severed unilaterally (left side) in Trial 1. In Trial 2, the sternal subcutaneous nerve trunk was severed either unilaterally (left or right side) or bilaterally. Four days postdenervation, FRF was determined bilaterally either antemortem (immediately prior to stunning) or 2 min after stunning and bleeding (postmortem). In Trial 1, the pectoral feather tract ante- and postmortem FRF values did not differ significantly for innervated or denervated tracts. In this trial, the sternal feather tract ante- and postmortem FRF values were 13% higher (44 g) for the denervated (left side) than for the innervated (right side) treatments. Partitioning this difference into the effects of sample side or innervation could not be attained because only the left side was denervated (left-denervation or right-innervated) in Trial 1. In Trial 2, both the left and right sternal feather tracts were represented in equal numbers for the innervated and denervated treatments, and there were no significant differences in FRF related to innervation, left and right side, or ante- and postmortem sample times. The presence or absence of cutaneous nerve innervation does not appear to influence FRF ante- or postmortem. This finding indicates that treatments disabling the central nervous system antemortem may lower FRF indirectly by altering cutaneous metabolism and therefore have been consistently unsuccessful in substantially altering postmortem FRF.

Close link between cutaneous nerve pattern development and feather morphogenesis demonstrated by experimental production of neo-apteria and ectopic feathers: implication of chondroitin sulphate proteoglycans and other matrix molecules.

In chick skin, nerve arcades develop around the base of feathers. In order to understand the mechanisms of their formation, we have tried to dissociate arcade formation from feather morphogenesis in various ways. Nerve patterns were analysed (1) in hydrocortisone-treated embryos that are partially devoid of feathers, (2) after retinoic acid treatment that produces ectopic feathers, (3) in dorsal root ganglia-skin co-cultures. Whenever tested, immunochemistry revealed that nerve arcades form around chondroitin sulphate proteoglycan-rich areas. Hydrocortisone treatment modifies the distribution of two out of three chondroitin sulphate proteoglycan epitopes tested, as well as the shapes of the feathers and nerve arcades, but not fibronectin, tenascin or laminin localizations. Chondroitinase digestion in co-cultures eliminated the nerve arcade formation and produced abnormally thin feathers, but nevertheless with a normal spatial distribution. Thus, chondroitin sulphate proteoglycans are probably not involved in the overall arrangement of feathers, but appear to play a fundamental role in both the formation of nerve arcades and the morphogenesis of the feather.

[Development of the cutaneous nervous system]. / Développement du système nerveux cutané.

Skin of vertebrates is richly innervated, mainly by sensory nerve fibres which form a well organized pattern, particularly around phaners. This innervation develops segmentally (dermatomes) from cutaneous branches provided by spinal nerves. The innervation begins at 13 days (E 13) in the mouse embryo and, although hair buds form at E 16, follicles are only innervated from 5 days postnatally being complete at about 20 days. In the chick skin, innervation forms a regular and characteristic pattern around feathers, and can be visualized on whole mounts. Its development can be traced from 6 days of development in relation to feather morphogenesis. Experiments producing non formation of spinal ganglia (X-ray irradiation or neural tube ablation) or production of neoapteria (hydrocortisone treatment) or ectopic feathers on scales (retinoic acid treatment) show there is a close link between feather development and nerve pattern formation. In vitro co-cultures of dorsal root ganglia and epidermis combined with the use of synthesis inhibitors and antibodies, showed that epidermis has a repulsive effect on nerve fibres mediated, at least in part, by chondroitin sulphate proteoglycans. These compounds have been localized, using antibodies mainly at the base of the feather buds and seem to play a key role in the construction of the fine nerve pattern around feather follicles. In conclusion, the specific nerve patterns are the final result of selective responses of growing nerve endings to unique combinations of local cues and conflicting interactions which are developmentally regulated in parallel with the morphogenesis of phaners.

Peripheral projections of a subpopulation of dorsal root ganglion neurons defined by ovalbumin immunoreactivity.

Previous studies from this laboratory have used antisera to aldehyde-conjugated ovalbumin to localize ovalbumin-like immunoreactivity within a subpopulation of sensory neurons. We have now combined retrograde tracing and immunohistochemical procedures to identify the tissues innervated by sensory neurons which are either immunoreactive or non-immunoreactive for ovalbumin. The fluorescent tracer Di-I was administered to feather follicles, flexor ulnar muscle, subdermis, expansor secundariorum, heart and liver and identified seven days later within corresponding dorsal root ganglia. Most neurons innervating the follicles had large cell somata, and fewer than 3% were immunoreactive for ovalbumin. In contrast, most sensory neurons projecting to subdermis, muscle and expansor secundariorum muscle were of a medium diameter. Approximately 25% of those neurons projecting to the expansor secundariorum, and 60% projecting to the subdermis and muscle, were immunoreactive for ovalbumin. Sensory neurons innervating heart and liver were the smallest, and only 8% were immunoreactive for ovalbumin. The study indicates that sensory neurons innervating different organs have somata with significantly different sizes, suggesting a functional specificity. Moreover, neurons demonstrating either the ovalbumin-IR positive or negative phenotypes show distinct peripheral projections, suggesting that this phenotype may be at least partially controlled by retrograde signals derived from the cells they innervate.

[Participation of the nucleus epibasalis centralis in regulating the function of the skin-feather complex of poultry]. / Uchastie n. epibasalis centralis v reguliatsii funkstional'nogo sostoianiia kozhno-per'evogo kompleksa ptits.

In acute experiments on anesthetized mature chickens, the bioelectrical activity of epibasal neurons was influenced upon both by means of intradermal histamine injections and direct histamine application to the medial region of n. epibasalis centralis, as well as by uni- and bilateral lesion of this structure. The processes under study were evaluated with respect to the parameters of focal potentials and neuronal reactions induced in n. epibasalis centralis as well as by the measurement of the feather adhesive force, the latter being a correlate for the skin analyzer sensibility. It is shown that the feather adhesive force increases with growing activity of the central neurons and decreases in case of their activity suppression or lesion of the nucleus.

Sensory receptors and their afferents in the caudal sympathetic nerve of the domestic duck.

The behavioural reactivity of the visceral receptors and their afferents in the caudal sympathetic nerve (part of synsacral sympathetic chain) of domestic duck (Anas platyrhynchos) was studied using electrophysiological techniques to examine their involvement in different physiological functions. In total, 114 single unit activities were recorded from the caudal sympathetic nerve of duck. Receptors were classified according to location: in the anal sphincter (32 units), in the mucous membrane of the cloaca (45 units), at the branching point of the blood vessels over the rectum and adjacent mesentery (10 units), at the base of the feather follicles in and around the vent (17 units), and in the ventral and lateral lower abdominal wall muscle (10 units). Both spontaneous and non-spontaneous receptors responded to mechanical stimuli; average frequency of discharge of non-spontaneous units being much higher. Most of these receptors were of the rapidly-adapting type. Only some receptors in the abdominal muscle layer, anal sphincter and mucous membrane of hind gut were of the slowly-adapting type. Some of the latter responded to intraluminal distension pressure. Except for responses to succinylcholine chloride by receptors in the abdominal wall muscles and some units in the external anal sphincter, mechanosensitive receptors were not responsive to chemical stimuli. The discharge rate of the receptors at the base of the feather follicles varied according to the strength of stimulus. Conduction velocity of the caudal sympathetic afferent fibres ranged from 2.5 to 45 m/sec.