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At least 19 recordsLinked to original sources
PubMed1989

A comparison of sperm morphology and silver nitrate staining characteristics in the domestic ferret and the black-footed ferret.

Ejaculated sperm from the domestic ferret (Mustela putorius furo) and the black-footed ferret (Mustela nigripes) were compared for differences in morphological abnormalities and argentophilic protein distribution. Thawed domestic ferret sperm was also compared to fresh sperm to determine whether there were any effects on cell morphology due to cryopreservation. There were statistically significant differences between the two species of ferret in two of the categories scored. The domestic ferret had a higher frequency of cells that were bent in the midpiece and in the principal piece, and a higher frequency of headless and tailless cells when compared to the black-footed ferret. There were no statistically significant differences in cell morphology between the fresh and cryopreserved ejaculates of the domestic ferret employing a standard egg yolk cryoextender. Silver nitrate staining distribution was different between the two species in both the head and tail region.

Animals↗
PubMed1992

Comparative vaginal cytology of the estrous cycle of black-footed ferrets (Mustela nigripes), Siberian polecats (M. eversmanni), and domestic ferrets (M. putorius furo).

Vaginal cytology and vulva size were used to characterize the reproductive cycle of female black-footed ferrets (Mustela nigripes), Siberian polecats (M. eversmanni), and domestic ferrets (M. putorius furo). Emphasis was on black-footed ferrets because of the need to breed these critically endangered animals and on Siberian polecats because of the close taxonomic relationship to black-footed ferrets. Vaginal cytology of the 3 species of ferret is similar. Proestrus was characterized by an increasing percentage of superficial epithelial cells and enlargement of the vulva. During estrus, superficial cells were usually greater than or equal to 90% of epithelial cells in the vaginal lavage and after several days were fully keratinized. Neutrophils were more common during all stages of the estrous cycle in domestic ferrets than they were in the other species. Following copulation, percentage of superficial calls in the vagina declined and vulva swelling subsided. Large cells, probably of uterine symplasma origin, were observed in vaginal lavages following whelping or pseudopregnancy. Vaginal cytology is extremely useful in the reproductive management of black-footed ferrets and Siberian polecats. Knowledge of normal vaginal cytology could be applied to the diagnosis of female reproductive abnormalities in all 3 species.

Animals↗
PubMed1974

Immunity to influenza in ferrets. VII. Effect of previous infection with heterotypic and heterologous influenza viruses on the response of ferrets to inactivated influenza virus vaccines.

Normal ferrets did not produce serum antibody following immunization with 200 i.u. of inactivated A/Hong Kong/68 influenza virus vaccine and were found to be susceptible to subsequent challenge infection with A/Hong Kong/68 virus. High titres of virus were recovered from nasal washings collected 3 days after infection, serum antibody was produced, increased nasal protein was detected and HI antibody was detected in nasal washings. Ferrets infected with influenza virus A/PR/8/34 7 weeks before immunization with inactivated A/HK/68 virus did, however, produce serum HI antibody to A/HK/68 virus. This antibody conferred partial immunity to challenge infection with A/HK/68 virus, as shown by decreased titres of virus in nasal washings and reduced levels of nasal protein. Previous infection of ferrets with influenza virus B/Ann Arbor/66 did not result in the production of serum antibody to A/HK/68 virus following immunization with A/HK/68 vaccine and the animals were completely susceptible to subsequent challenge infection with A/HK/68 virus. Differences in the amount of nasal protein and nasal antibody produced after A/HK/68 infection were also found in ferrets previously infected with either A/PR/8/34 or B/AA/66 virus, compared with normal ferrets.

Animals↗
PubMed1974

Immunity to influenza in ferrets. X. Intranasal immunization of ferrets with inactivated influenza A virus vaccines.

The response of ferrets after intranasal inoculation of inactivated A/Hong Kong/68 (H3N2) influenza virus vaccines is reported. Normal ferrets given either saline vaccine in drops or freeze-dried vaccine in an aerosol intranasally did not produce detectable serum or nasal hemagglutination inhibiting antibody and were found to be completely susceptible to challenge infection with A/Hong Kong/68 virus. Intranasal saline vaccine did not produce an additive effect on the response of ferrets simultaneously given the same vaccine intramuscularly with adjuvant. Ferrets primed by previous infection with A/PR/8/34 (H0N1) influenza virus, however, responded to intranasal immunization with saline A/Hong Kong/68 virus vaccine and produced serum and nasal antibody. These animals were found to be partially resistant to challenge infection, in contrast to similar animals given saline vaccine intramuscularly which were completely resistant to challenge infection. Primed ferrets did not respond after immunization with the freeze-dried aerosol vaccine, but this may have been due to a failure of the aerosol to be inhaled satisfactorily.

Administration, Intranasal↗
PubMed1987

Restricted viral antibody specificity in many ferrets infected with the ferret Aleutian disease parvovirus. Brief report.

The majority of ferrets infected with a ferret strain of Aleutian disease virus (ADV) produce antibody only to a detergent-sensitive common determinant on the two closely related virion proteins. Ferrets with high antibody titers and mink infected with this virus also produce antibody to one or more virion immunogenic determinants unaffected by detergent.

Aleutian Mink Disease↗
PubMed1985

The electrocardiogram of normal ferrets and ferrets with right ventricular hypertrophy.

Sixty-eight electrocardiograms were recorded on ferrets (Mustela putorius furo). These represent 29 normal weanling males, 19 normal adult males and 20 adult males with right ventricular hypertrophy (RVH). Analyses of rate, rhythm, axis and total voltage were used to define the normal electrocardiogram (ECG) and to identify changes seen in RVH. The normal ferret has a heart rate of about 300 beats per minute and a mean electrical axis of + 86 degrees +/- 6.6 (SD). A 56% increase in right ventricular weight to body weight ratio was not associated with right axis deviation. The overall voltage produced on the ECG was increased in the group with RVH as compared to the normal group (p less than 0.030).

Animals↗
PubMed1985

Brugia malayi: intravenous injection of microfilariae in ferrets as an experimental method for occult filariasis.

Microfilaremia, immune responses, and pathology were compared in ferrets infected with 100 third-stage larvae of Brugia malayi (subperiodic strain) or injected intravenously with 10(6) microfilariae. Ferrets (Mustela putorius furo) inoculated with third-stage larvae typically became patent during the third month after infection, with a mean patency of 123 +/- 25 (SE) days. Ferrets injected intravenously with microfilariae exhibited a relatively constant microfilaremia for 3-4 weeks and usually cleared microfilariae before the fourth month. Ferrets that cleared microfilariae after intravenous injection of microfilariae or after infection with third-stage larvae failed to become patent or became amicrofilaremic within 3 weeks after a challenge intravenous injection of 10(6) microfilariae. Clearance of circulating microfilariae was associated with eosinophilia and serum antibody specific for the microfilarial sheath in ferrets injected with microfilariae and in most ferrets infected with third-stage larvae. Ferrets infected with third-stage larvae and necropsied after clearance of microfilariae had tissue inflammatory reactions to microfilariae characteristic of occult filariasis (tropical eosinophilia) in man; these ferrets exhibited immediate cutaneous hypersensitivity and circulating reaginic antibody to antigens of microfilariae. In ferrets necropsied following two intravenous injections of microfilariae, the majority of ferrets examined within 10 days after clearance of microfilariae had visible liver lesions to microfilariae identical to those of the ferrets infected with third-stage larvae; immediate cutaneous hypersensitivity and reaginic antibody were not consistently detected in ferrets injected with microfilariae. Sera from ferrets that had cleared circulating microfilariae were transferred passively into ferrets made microfilaremic by intravenous injection of microfilariae. Sera with microfilarial sheath-reactive IgG antibody titers (greater than or equal to 1:200) and microfilarial agglutination titers (greater than or equal to 1:40) rapidly cleared injected microfilariae (less than 24 hr); this serum also cleared or greatly reduced circulating microfilariae established by an infection with third-stage larvae; only the IgG-containing fraction of the sera was active in immune clearance. Sera that cleared microfilariae of B. malayi did not clear circulating microfilariae of Dirofilaria immitis or prevent recurrence of circulating microfilariae of B. malayi in ferrets infected with adult filariae.(ABSTRACT TRUNCATED AT 400 WORDS)

Agglutinins↗
PubMed1987

Evidence that a decrease in testosterone negative feedback mediates the pubertal increase in luteinizing hormone pulse frequency in male ferrets.

Neuroendocrine mechanisms regulating luteinizing hormone (LH) secretion during puberty were investigated in intact male ferrets and ferrets castrated at 8 wk of age that received s.c. implants of either empty or testosterone-filled Silastic capsules. To synchronize puberty onset among individuals, ferrets were exposed to short days between 8 and 16 wk of age, and then transferred to long days. Testis growth began in intact ferrets soon after photoperiod transition. Blood samples were obtained at 11, 15, 19, and 23 wk of age. LH pulse frequency was low in intact ferrets at 11 and 15 wk of age (less than or equal to 0.27 pulses/h), but rose to 0.94 pulses/h by 23 wk of age. No age-related increase in LH pulse frequency was observed in untreated castrated ferrets. LH pulses were rare in testosterone-treated castrated ferrets at 11 and 15 wk of age; but by 23 wk of age, frequency rose to 0.33 pulses/h. Thus, testis maturation in ferrets is accompanied by a dramatic increase in LH pulse frequency. No steroid-independent developmental increase in LH pulse frequency occurs in castrated ferrets. Furthermore, doses of testosterone that prevent LH secretion in young castrated ferrets do not as effectively suppress LH pulses in older ferrets. These data suggest that a decrease in the efficacy of testosterone negative feedback mediates the pubertal rise in LH pulse frequency in male ferrets.

Animals↗
PubMed1991

Distribution of choline acetyltransferase immunoreactive axons and terminals in the rat and ferret brainstem.

A survey was made of the density of the cholinergic innervation of different parts of the brainstem of the rat and ferret. Sections of rat and ferret brainstems were stained for choline acetyltransferase (ChAT) immunoreactivity by using a sensitive immunocytochemical method. Adjacent sections were stained for acetylcholinesterase activity or Nissl substance. The density of the distribution of fine calibre, varicose ChAT-positive axons, assumed to represent cholinergic terminals, was categorised arbitrarily into high, medium, or low. A high density of ChAT-positive terminals was found in all or parts of these structures: interpeduncular nucleus, superficial grey layer of the superior colliculus (ferret), intermediate layers of the superior colliculus, lateral part of the central grey (rat), an area medial to the parabigeminal nucleus (rat), pontine nuclei, ventral tegmental nucleus (rat), midline pontine reticular formation, and an area ventral to the exit point of the 5th nerve (ferret). A medium density of ChAT-positive terminals was observed in all or parts of: the substantia nigra zona compacta (ferret), ventral tegmental area (ferret), superficial grey layer of the superior colliculus, intermediate and deep layers of the superior colliculus, lateral central grey, area medial to the parabigeminal nucleus, inferior colliculus, dorsal tegmental nucleus, ventral tegmental nucleus (ferret), pontine nuclei, ventral nucleus of the lateral lemniscus (ferret), midline pontine reticular formation, ventral cochlear nucleus, dorsal cochlear nucleus, lateral superior olive, spinal trigeminal nuclei, prepositus hypoglossal nucleus, lateral reticular nucleus, paragigantocellular nucleus, and the dorsal column nuclei including the cuneate, external cuneate, and gracile nuclei. A low density of ChAT-positive terminals was seen throughout the remainder of the brainstem of the rat and ferret, but these terminals were absent from the medial superior olive, substantia nigra zona reticulata (rat), and the central part of the ferret lateral superior olive. A pericellular-like distribution of ChAT-positive terminals was observed in the ventral cochlear nucleus and in association with some of the cells of the nucleus of the mesencephalic tract of the trigeminal nerve. A climbing fibre type arrangement of ChAT-positive terminals was found in the substantia nigra zona compacta (ferret) and medial reticular formation. In general, the distribution of staining for AChE activity reflected that of the distribution of ChAT immunoreactivity in the brainstem, except in a few regions where there were also species differences in the distribution of ChAT-positive terminals, e.g., in the superficial grey layer of the superior colliculus and in the substantia nigra.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1986

Antibody and cellular immune responses to microfilarial antigens in ferrets experimentally infected with Brugia malayi.

Eleven of 15 ferrets experimentally infected with Brugia malayi became amicrofilaremic after a brief patency; only four ferrets remained patent after 6 months of infection and two of these ferrets developed a high, persistent microfilaremia. Blastogenic responses of peripheral blood lymphocytes to antigens of microfilariae (mf), assayed in vitro, demonstrated an antigen sensitivity at prepatent, patent and postpatent periods of infection. Lymphocytes from ferrets with high microfilaremia had elevated background responses in culture which were directly correlated with the number of circulating mf. This background response was attributed to antigenic stimulation by mf present in the lymphocyte cultures; addition of mf to cultures of lymphocytes from postpatent ferrets induced responses equivalent to those observed in microfilaremic ferrets. Lymphocyte responses to the mitogen, concanavalin A, did not differ significantly among microfilaremic, amicrofilaremic and uninfected ferrets. Antibody in IgG to antigens of mf measured by ELISA and by immunoblots from SDS-PAGE showed similar patterns of response in ferrets which became amicrofilaremic and in the few ferrets which remained microfilaremic. prausnitz-Kustner tests demonstrated no consistent differences in titers to microfilarial antigens between patent and amicrofilaremic ferrets. The results suggest a high level of immune responsiveness to antigens of mf in infected ferrets with no evidence of immunosuppression associated with prolonged microfilaremia or of major changes in immune responses with development of amicrofilaremic infections.

Animals↗
PubMedDate not supplied

Effect of upper respiratory infection on hearing in the ferret model.

In an effort to develop an adult animal model for acquired viral-induced hearing loss, three groups of mature ferrets were inoculated intranasally with respiratory viruses (influenza A/Port Chalmers, influenza B/Mass, and parainfluenza I), which have been implicated as causative agents in idiopathic sudden hearing loss (ISHL). All ferrets challenged with influenza A/Port Chalmers (A/PC) exhibited clinical signs of infection, but neither of the other two groups exhibited such signs. Conductive and/or sensorineural hearing losses were demonstrated in eight of 15 ferrets challenged with influenza A/PC and four of 10 ferrets in the group challenged with influenza B/Mass by brainstem auditory-evoked responses (BAERs) and acoustic immittance. None of the four ferrets infected with parainfluenza I demonstrated auditory dysfunction. When auditory changes were observed, nasal washes were performed, and tissues of the middle and inner ears were collected for viral assay and morphologic examination. All ferrets demonstrating auditory changes were shown to be infected by isolation of virus from nasal tissues. Virus was isolated from eustachian tube tissue in six of the eight ferrets infected with influenza A/PC, which also demonstrated altered BAERs and one of the four infected with influenza B/Mass, which also had auditory changes. Virus was isolated from the middle ear of two ferrets infected with influenza A/PC and from the inner ear of another two ferrets from the same group. These data suggest that influenza A/PC has a greater effect on auditory function in the ferret model than either influenza B/Mass or parainfluenza I and that the ferret may be an appropriate adult model to examine the etiologic role of viral upper respiratory tract infections in some acquired hearing impairments.

Acoustic Impedance Tests↗
PubMed1990

Photoperiodic regulation of gonadal growth and pulsatile luteinizing hormone secretion in male ferrets.

Testicular growth was monitored in male ferrets subjected to one of the following photoperiodic treatments begun at weaning (8 weeks of age): 8 hr light/day (short days), 18 hr light/day (long days), or short days followed by transition to long days at either 10, 12, or 14 weeks of age. Mean ages to achieve adult testis width of greater than or equal to 12 mm were 27.5 +/- 1.3, 25.0 +/- 1.5, 23.6 +/- 2.9, 20.0 +/- 0.8, and 21.2 +/- 1.0 weeks in ferrets raised from weaning in long days, raised from weaning in short days, and transferred from short to long days at 10, 12, or 14 weeks, respectively. This criterion was met significantly earlier by ferrets experiencing the photoperiod transition at 12 or 14 weeks of age than by ferrets housed in long days from weaning. At the end of the experiment (30 weeks of age), mean testis width was significantly smaller in ferrets raised in long days from weaning or transferred to long days at 10 weeks of age, compared to that of the other three groups (p less than 0.05). In a second experiment, photoperiod experience with long or short days was begun at birth, and testicular size was monitored for a longer period of time. The time courses for testicular maturation were similar to that obtained when these treatments began at weaning. By 40 weeks of age, mean testis width of ferrets raised in long days was comparable to that of ferrets raised in short days. A third study determined that the retarded testicular growth observed in ferrets exposed to long days from weaning was correlated with diminished pulsatile luteinizing hormone (LH) secretion. At 28 weeks of age, mean LH pulse frequency was 0.86 +/- 0.09 pulses/hr in ferrets undergoing spontaneous puberty in short days or photoinduced puberty after a short-to-long-day transition; pulse frequency was significantly lower (0.46 +/- 0.26 pulses/hr; p less than 0.05) in ferrets raised in long days. These results indicate that gonadal growth can be precociously induced in male ferrets by exposure to a sequence of short days followed by long days, and that the absence of sufficient prepubertal exposure to short days compromises pulsatile LH secretion and rate of gonadal growth. Experience with short days during development may be necessary for manifestation of stimulatory responses to long days.

Aging↗
PubMed1985

Morphology, central projections, and dendritic field orientation of retinal ganglion cells in the ferret.

Retinal ganglion cells were studied in pigmented ferrets that received small electrophoretic injections of horseradish peroxidase (HRP) into the dorsal lateral geniculate nucleus (LGNd) or optic tract. Ferret retina contains a number of types of retinal ganglion cells of which the relative cell body sizes, dendritic field structures, and central projections correspond closely to those of retinal ganglion cell types in the cat. Ferret retina contains about the same proportion of alphalike cells, a lower proportion of betalike cells, and thus a high proportion of other types of ganglion cells than cat retina. Ferret retina has a visual streak and somewhat weaker area centralis than cat retina. Changes in ganglion cell morphology associated with eccentricity are less pronounced in the ferret than in the cat. The adult ferret retina is about 12.5 mm in diameter, and the nasotemporal division is about 2.7 mm from the temporal margin. Interestingly, virtually all alpha cells in the pigmented ferrets studied projected contralaterally. Studies of infant ferrets indicate that 4 days after birth (P4) the area of ferret retina is 25% that of the adult. The neonatal ferret retina contains numerous small, densely packed cells in the presumptive ganglion cell layer. At P4 these cells appear to be uniformly distributed across the retina. The area centralis and visual streak are not obvious as late as 8 days after birth.

Animals↗