New data on the taxonomy of the Brazilian marmosets of the genus Callithrix Erxleben, 1777.
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No significant correlation exists between the amount of biologically active marmoset chorionic gonadotrophin (mCG) in urine and results obtained with an immunological pregnancy test. The pregnant marmoset excretes large amounts of oestrogenic steroids, which must be removed, to prevent the enhancement of the response of the bioassay for mCG. More than 99% of these unconjugated and conjugated urinary oestrogens can be removed by extraction with acetone and ether. mCG is excreted throughout pregnancy, maximum levels occurring between the 8th and 9th week of gestation. There is a considerable within- and between-animal variation in the amount of mCG excreted. However, the pattern of gonadotrophin excretion by the pregnant marmoset is similar to that of man and the apes but unlike that of baboons and macaques.
16 pairs of common marmosets were formed, six of which were observed for 7 weeks, and ten for 4 weeks. A variety of behaviours was recorded, including sexual mounting, male tongue-smacking, female slit-eyed tongue-flicking, scent marks, huddling, allogrooming and autogrooming. Behaviours associated with sexual encounters occurred initially at high levels but declined during the study period. The incidence of sexual mounting was closely related to that of male tongue-smacking and female slit-eyed tongue-flicking. Other social behaviours including scent-marking and allogrooming did not show a consistent pattern of occurrence with respect to time or sexual activity.
The breeding records of a closed colony of marmosets maintained for five years are described. Three generations have been born and a high incidence of multiparity has been achieved. The reproductive potential of C. jacchus is higher than that of virtually any other primate maintained in captivity.
Teeth from 18 marmosets, seven months to 5.8 years of age, were studied histologically. A minimum of one dark and one light band comprised one cemental annulation. Age was estimated by counting the number of annulations and adding four months to premolar and eight months to canine teeth for tooth development. Cemental annulations were most consistent near the gingival border on the labial aspect of the tooth. The method will be valuable in estimating the ages of marmosets and other nonhuman primates.
Exogenous luteinizing hormone-releasing hormone (LH-RH) administered in a wide range of doses (0.2-25 micrograms) to intact male marmoset monkeys induced a marked increased in plasma luteinizing hormone (LH) concentrations. Maximum LH concentrations achieved after injection of LH-RH occurred progressively later as the dosage increased. Bilateral orchidectomy sigificantly enhanced pituitary responsiveness to a standard dose (2.0 microgram) of LH-RH, whereas the introduction of oestradiol-17 beta implants effectively inhibited the responses. LH-RH-induced LH release after gonadectomy (with and without oestradiol-17 beta treatment) was similar in males and females. The use of marmosets for appropriate investigation into the physiological role of LH-RH in controlling LH secretion in primates is proposed.
All adult marmosets tested had ureaplasmas in their throats but not in the lower respiratory tract, and rarely in the genital tract. Ureaplasmas persisted in the throat of a marmoset separated from the colony for 44 days. They could not be recovered from the animals for at least nine weeks after a course of minocycline. Airborne reinfection did not occur when these animals were surrounded by, but separate from, infected marmosets. It occurred when the minocycline-treated animals were caged with the infected marmosets or were inoculated. The genital tract was more difficult to infect than the oropharynx.
In an earlier report (Chapman et al, Biochemistry 1979;18:5096-5108), we suggested that the common marmoset may represent an important model for the study of human plasma lipoprotein metabolism. We now extend the interest of this monkey model to the study of lipoprotein(a) (Lp[a]) and apolipoprotein(a) (apo[a]). Density gradient ultracentrifugal fractionation of marmoset plasma revealed a bimodal distribution of Lp(a), with one peak of concentration occurring in association with very low density lipoproteins (VLDLs) and a second in the density range 1.040-1.080 g/ml. The dense Lp(a) subspecies displayed physicochemical properties (chemical composition, particle size, and electrophoretic mobility) that closely resembled those of its counterpart in humans and baboons but that were distinct from those of low density lipoprotein (LDL). Furthermore, the particle size of marmoset Lp(a) was invariant (31 nm) over the density interval 1.040-1.080 g/ml, whereas that of LDL decreased progressively with an increase in density (approximately 26-25.2 nm). Use of polyclonal and monoclonal antibodies to human apo(a) and of a polyclonal antibody to marmoset Lp(a) allowed immunologic identification of a single apo(a) isoform in the marmoset whose size was similar to that of apo B-100; apo(a) and apo B-100 were associated in Lp(a) particles by a disulfide linkage. The total protein mass of apo-Lp(a) was estimated to be 800,000 or more by electrophoresis in sodium dodecyl sulfate-polyacrylamide-agarose gels. The amino acid compositions of marmoset and human apo(a) resembled each other but were distinct from those of the corresponding forms of apo B-100. Immunologic evidence is provided for a high degree of cross reactivity between apo(a) in marmosets, baboons, and humans, supporting the idea of the existence of a marked degree of structural homology between these proteins. In addition, electroimmunoblotting of marmoset apo(a) and marmoset plasminogen showed that these proteins shared certain epitopes in common, suggesting that marmoset apo(a) may possess kringle-like structural features. Finally, despite possession of a single apo(a) isoform, marmoset Lp(a) levels varied over a 100-fold range (0.5-49 mg/dl plasma). Considered together, our present findings suggest that the common marmoset monkey constitutes a unique model in which to study the regulation of apo(a) gene expression and the posttranslational processing of apo(a), as well as factors that modulate the synthesis, intravascular metabolism, and cellular catabolism of Lp(a).
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By allowing families to increase in size, co-operation between parents and adolescents in infant care was encouraged. Young adult pairs were subsequently created with these marmosets which had experience of handling infants to provide a stable basis for breeding 2nd and 3rd generation marmosets in captivity.
An intramuscular dose of 18 mg/kg bodyweight of this steroid anaesthetic produced surgical anaesthesia with rapid induction, safe, efficient maintenance and rapid recovery without side effects.
3 techniques for studying reproductive function in the marmoset are described. Abdominal palpation was found to be the most successful method for diagnosis of pregnancy. Vaginal cytology and urinary immunoassays met with limited success and were of supportive value only.
Qualitative and quantitative measurements of skeletal development were performed on foetal marmosets in utero and on fixed specimens of both foetuses and neonates. The sequence of skeletal changes may be used to assess developmental status and the prenatal growth of the marmoset is compared with that of other primate species.
The rectal temperature of 8 marmosets was taken regularly throughout a 76 hour period. A pronounced circadian rhythm was detected: body temperature reached a maximum during the light phase and a minimum during the dark phase.
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During 1983 a severe episode of respiratory infection occurred in a marmoset colony at these laboratories. Of 91 marmosets, 69 showed clinical signs of disease, one died and nine were so ill that euthanasia was necessary. Eight were examined post mortem and all showed consolidation of the lungs. Laboratory studies were carried out in an attempt to establish the cause of the outbreak and an interstitial pneumonia was found in seven animals which were examined histologically. Direct electron microscopy of nasal swabs and lung samples revealed the presence of a high titre of a paramyxovirus, and subsequent immunofluorescence studies established that the particular paramyxovirus involved was parainfluenza virus type I. Subsequent studies showed that surviving affected animals had seroconverted to parainfluenza I virus while animals that had not been implicated in the outbreak had not.