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1.
Theriogenology ; 79(4): 640-6, 2013 Mar 01.
Article in English | MEDLINE | ID: mdl-23265930

ABSTRACT

Although slow release GnRH-agonist implants have been shown to effectively suppress the estrous cycle in queens, there are still several remaining questions about their use: if the probability and frequency of estrus induction because of initial stimulation is dependent on the stage of cycle when animals are treated, if all effects are reversible, and to what extent fertility is regained after the end of efficacy. The latter is of major interest to cat breeders who want temporary suppression of estrus in breeding animals. Twenty queens (14 with known fertility) were treated with a 4.7 mg deslorelin implant; hormonal changes (progesterone [P4], and estradiol [E2]) and behavioral changes with special respect to estrus signs and subsequent fertility were assessed. Group A cats (N = 10) were treated 3.2 ± 0.8 days after the beginning of estrus and estrus stopped 4.1 ± 2.5 days after treatment. Estrus induction was observed in one queen 6 days after treatment, and one queen showed estrous signs 138 and 155 days after treatment. Progesterone increased significantly after treatment in all animals until day 14, then slowly decreased reaching basal levels on day 56 without any further increase. Group B cats (N = 10) were treated 7 days after the end of estrus; nine cats had P4 > 1.5 ng/mL and basal E2, one cat (B10) had basal E2 and P4. In cat B10 estrus induction occurred after treatment, but in none of the others; however, E2 increased in all group B cats 1 day after treatment but reached pretreatment concentrations on Day 7 again and remained basal. The implant was still effective in one animal of the estrus group with a duration of efficacy >1102 days, in the others duration of efficacy varied between 483 and 1025 days. Eight queens were mated afterwards and gave birth to a healthy litter with 3.3 ± 1.5 kittens. This study proves that (1) the incidence of estrus induction-although very low-is highest after treatment in estrus or postestrus, (2) the duration of efficacy varies between 16 and 37 months, and (3) estrus suppression is reversible and animals remain fertile after the treatment effect has expired.


Subject(s)
Cats/physiology , Contraception/veterinary , Contraceptive Agents, Female/administration & dosage , Estrus , Gonadotropin-Releasing Hormone/agonists , Triptorelin Pamoate/analogs & derivatives , Animals , Contraception/methods , Drug Implants , Estradiol/blood , Female , Fertility , Pregnancy , Progesterone/blood , Triptorelin Pamoate/administration & dosage
2.
J Feline Med Surg ; 13(8): 577-87, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21802033

ABSTRACT

Chronic caudal stomatitis with alveolar/buccal mucositis in calicivirus-positive cats is the most severe presentation of feline chronic gingivostomatitis. Refractory cases are helped by antibiotic and anti-inflammatory treatments often including glucocorticoids. In order to evaluate the comparative efficacy of oromucosal administration of recombinant feline interferon omega (rFeIFN-ω) versus oral administration of glucocorticoids, a randomised, multi-centre, controlled, double-blind study was performed in 39 cats. The progression of behavioural, clinical and lesional scores was assessed over 90 days. Daily oromucosal treatment with 0.1 MU of rFeIFN-ω was associated with a significant improvement of clinical lesions (caudal stomatitis and alveolar/buccal mucositis) and a decrease of pain scores from D0 to D90. Although no such statistical improvement was noticed in the prednisolone group, there was, however, no significant difference between the two groups for most of the parameters, except pain at D60 and D90.


Subject(s)
Caliciviridae Infections/drug therapy , Glucocorticoids/therapeutic use , Interferon Type I/therapeutic use , Prednisolone/therapeutic use , Stomatitis/veterinary , Administration, Oral , Animals , Caliciviridae Infections/complications , Calicivirus, Feline/genetics , Calicivirus, Feline/isolation & purification , Cats , Double-Blind Method , Female , Interferon Type I/standards , Male , Real-Time Polymerase Chain Reaction/veterinary , Stomatitis/drug therapy , Stomatitis/virology , Tooth Extraction/adverse effects , Tooth Extraction/veterinary , Treatment Outcome
3.
Theriogenology ; 75(5): 803-10, 2011 Mar 15.
Article in English | MEDLINE | ID: mdl-21196037

ABSTRACT

The aim of the present study was to test for the efficacy of a slow release GnRH-agonist implant (4.7 mg deslorelin, Suprelorin) in the male cat. Ten toms were implanted sc in the neck. Changes in testosterone (T) secretion, testicular size, body weight and behaviour (mounting, mating, urine marking) were monitored. T concentrations were significantly decreased (P < 0.0001) to basal levels (< 0.1 ng/mL) in 5 of 10 cats after 4 weeks and in all but one tom after 11 weeks (T < 0.1 ng/mL). In this respective tom only partial downregulation with T-values from 0.2 to 0.1 ng/mL was achieved until week 27. In weeks 28 and 32, T concentrations were below 0.1 ng/mL. Compared to pretreatment values, testicular volume was significantly decreased by about 60% in week 12 and about 73% after 36 weeks (P < 0.001). Penile spines disappeared 9.4 ± 1.0 weeks after treatment. Food intake was significantly increased during treatment period (P < 0.001). In all tomcats libido, mating behaviour and urine marking were significantly reduced (P < 0.0001) after an initial stimulation. In one tom, mating an oestrous queen on day 20 after implant administration resulted in pregnancy. Mating of another tom that had T-values between 0.1 and < 0.1 ng/mL since day 24 in week 8 revealed the presence of spermatozoa; however, this mating did not result in pregnancy. Subcutaneous implant administration was well tolerated by all tomcats without sedation or anaesthesia and no treatment related negative effects were observed. These results demonstrate the clinical efficacy of the 4.7 mg deslorelin implants (Suprelorin) in the tom inducing all castration related effects.


Subject(s)
Cats , Contraception/veterinary , Gonadotropin-Releasing Hormone/agonists , Orchiectomy/veterinary , Reproduction/drug effects , Triptorelin Pamoate/analogs & derivatives , Animals , Body Weight/drug effects , Contraception/methods , Drug Implants , Eating/drug effects , Male , Orchiectomy/methods , Sexual Behavior, Animal/drug effects , Testis/anatomy & histology , Testis/drug effects , Testosterone/blood , Triptorelin Pamoate/administration & dosage , Triptorelin Pamoate/adverse effects
4.
Vet Dermatol ; 20(5-6): 405-11, 2009 Oct.
Article in English | MEDLINE | ID: mdl-20178477

ABSTRACT

This double-blind controlled study assessed whether reduced doses of omega interferon (rFeIFN-omega) (Virbagen Omega) could improve the clinical signs of canine atopic dermatitis (CAD) over a 6-month period, in comparison with cyclosporin. Thirty-one dogs diagnosed with CAD were entered in the study. Complicating infections were treated prior to entry. Dogs received 10 injections of rFeIFN-omega (1-5 million units according to bodyweight) or placebo over 6 months, and placebo capsules or cyclosporin (5 mg/kg) once daily for 2 months and then twice weekly for 4 months in groups 1 and 2 respectively. Flea control, non-medicated shampooing and ear cleansing were performed regularly. If a bacterial infection or Malassezia overgrowth developed, it was treated with oral cephalexin or with 3% chlorhexidine shampoo respectively. Oral prednisolone was used before day 90 to relieve pruritus when required for humane reasons (1 mg/kg once daily for 7 days). The CADESI-03 and a pruritus index were evaluated on day (D) 0, D14, D35, D56, D90, D120 and D180. No significant difference was detected between the groups for the time courses of lesions or pruritus over 6 months. On D90, the proportions of dogs with > or =50% improvement of pruritus and lesion scores were 56% and 72% respectively with interferon, 75% and 75% respectively with cyclosporin. Five dogs from group 1 and two dogs from group 2 were withdrawn from the study for treatment failure. Both products were well tolerated. Treatment with rfeIFN-omega at low doses may help for the long-term management of CAD.


Subject(s)
Dermatitis, Atopic/veterinary , Dog Diseases/drug therapy , Immunosuppressive Agents/therapeutic use , Interferon Type I/therapeutic use , Animals , Cyclosporine/adverse effects , Cyclosporine/therapeutic use , Dermatitis, Atopic/drug therapy , Dogs , Double-Blind Method , Drug Administration Schedule , Female , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/adverse effects , Interferon Type I/administration & dosage , Interferon Type I/adverse effects , Male , Recombinant Proteins
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