Ovariohysterectomy requires more post-operative analgesia than orchiectomy in dogs and cats.

The requirement for post-operative analgesia after ovariohysterectomy (OH) versus orchiectomy in dogs and cats was compared. Twelve male and 12 female cats and 12 male and 12 female dogs received meloxicam, 0.1 mg/kg body weight, PO, 2 h before surgery. Eleven female cats and 3 female dogs received rescue analgesia (P = 0.002). No male of either species required rescue analgesia. The number of cats receiving rescue analgesia was greater in females than in males (P < 0.0001). One should not rely solely on preoperative short-acting opioid and preemptive use of NSAIDs to control postoperative pain following OH, in dogs or cats. Postoperative pain after OH should be assessed for at least 2 h for cats and 4 h for dogs, using species-specific validated tools, to ensure proper postoperative pain diagnosis and management. Male dogs and cats subjected to orchiectomy required less postoperative analgesia intervention than female dogs and cats submitted to OH.

L'ovariohystérectomie nécessite d'avantage d'antalgiques post-opératoires que l'orchiectomie chez les chiens et les chats. Dans cette étude, nous avons comparé le besoin en antalgiques post-opératoires après l'OH versus l'orchiectomie chez les chiens et les chats. Douze mâles et 12 femelles, chats et chiens, ont reçu 0,1 mg/kg de Méloxicam par voie orale, 2h avant chirurgie. Onze chattes et trois chiennes ont eu besoin d'antalgiques de secours (P = 0,002). Aucun mâle de l'une ou l'autre espèce n'en a eu besoin. Chez les chats, les besoins en antalgiques de secours étaient plus élevés chez les femelles que les mâles (P < 0,0001). Il est donc primordial de ne pas se fier uniquement aux opioïdes à action courte préopératoire, et à l'utilisation préventive des AINS, pour contrôler la douleur post-opératoire après OH, tant chez le chien que chez le chat. L'évaluation de la douleur post-opératoire après l'OH devrait être suivie pendant au moins 2 heures pour les chats, et 4 heures pour les chiens, en utilisant des outils validés et spécifiques pour chaque espèce, afin d'assurer un diagnostic et une prise en charge post-opératoire appropriés à la douleur. Chez les chiens et les chats, les mâles soumis à l'orchiectomie ont nécessité moins d'intervention d'antalgiques post-opératoires que les femelles soumissent à l'OH.(Traduit par les auteurs).

Sex steroid receptors and apoptosis-related proteins are differentially expressed in polycystic ovaries of adult dogs.

In Polycystic Ovaries (PCOs), the dynamics of sex hormone receptors and follicle-related apoptotic signaling remain unknown. In this study, we investigated the expression of androgen receptors (AR), estrogen receptors (ERα and ERß), and apoptosis-related molecules (BAX, active caspase-3, Bcl-2 and Survivin) on different follicular stages of PCOs in adult dogs. Clinical evidences of high estradiol and testosterone levels, persistent estrus and vaginal discharge were observed. Inhibin B immunolabeling was increased in primary and 2 to 5-mm follicles, and a marked epithelial hyperplasia was common in the ovarian surface. Ovarian epithelia and primary follicles showed low expression of AR, ERα, and ERß, whereas a moderate immunoexpression of AR was found in theca cells of secondary follicles and cysts. In PCOs, growing follicles displayed ERα expression, and secondary follicles exhibited higher ERß expression. In addition, while few ERα-positive cells were found in the cysts, ERß was moderately expressed in growing follicles and cysts. BAX was upregulated in the ovarian epithelium, primary follicles, and in the wall of follicular cysts. Active caspase-3 was significantly downregulated in the epithelium, primary follicles, and follicular cysts, whereas growing follicles had a strong immunoexpression in the granulosa cells. Bcl-2 and survivin were increased in the epithelium and primary follicles, and only survivin was upregulated in secondary and growing follicles. While Bcl-2 had a diffuse immunexpression in the follicular cysts, survivin was overexpressed by these cells. We concluded that sex steroid receptors and apoptotic proteins are differentially expressed in the follicles of adult dogs with PCOs.