Martina Gallo

Increasing evidence supports a pathogenic role of heparan sulphate (HS) in the development of dementia. Since HS proteoglycans are present in the endothelial cells and perivascular basement membrane, we wanted to assess blood titres of HS antibodies (Abs) in patients with vascular dementia (VD) and in patients with Alzheimer's disease (AD) with cerebrovascular disease (CVD) [mixed dementia (MixD)]. Moreover, plasma levels of homocysteine, an independent risk factor for the development of dementia as well as for CVD, were also determined. High HS Abs titres were present in one patient with VD and in two patients with mixed dementia, as well as in two neurological control patients (stroke and epilepsy). Increased homocysteine levels were found in 62.5% of patients with mixed dementia, in 22.2% of the VD subjects, in 54.2% of patients with CVD, and in 41.2% of patients with other neurological diseases. The present findings suggest that neither elevated HS Abs titres nor increased homocysteinemia may represent a useful biochemical marker for the diagnosis of VD.

Tramadol is a synthetic codeine analogue used as an analgesic in human and veterinary medicine, but not approved for use in cats. Tramadol (2 mg/kg) was administered intravenously (IV) as preoperative analgesic in 12 cats (6 males) undergoing surgical gonadectomy. The pharmacokinetic profile of the drug and its O-desmethyl metabolite were determined in 8 animals (4 males), while intraoperative effects and postoperative analgesia, estimated by subjective pain score (0-24), were evaluated in all. Mean intraoperative isoflurane consumption was reduced, but hypoventilation was not observed. Sex-related differences were not observed, particularly in terms of postoperative analgesia: rescue analgesic was never administered. Concentrations of the active O-desmethyl metabolite were persistently high in all the animals. Considering the results obtained in this study, tramadol, at the dose of 2 mg/kg IV, did not produce any evident intraoperative cardiorespiratory side effects and with additional investigation may prove to be an appropriate intraoperative analgesic in cats undergoing gonadectomy.

IntroductionPropofol (PRO) is a short-acting, intravenous anaesthetic drug. It is usually used to induce and/or maintain general anaesthesia or to produce sedative effects during local/regional anaesthesia. At low doses, PRO has anti-emetic and anti-convulsive properties. Due to its high lipophilicity, PRO distributes rapidly from blood to tissues and crosses the hematoencephalic barrier in a very short time. These properties, together with its extensive hepatic metabolism, explain the very rapid induction of anaesthesia and the short-lasting effects of PRO. Maintenance of general anaesthesia can be achieved by continuous PRO infusion or by repeated administrations in bolus (Langley and Heel 1988; Dawidowicz et al. 2006). The main mechanism of action of PRO consists of the enhancement of GABA-A mediated inhibitory effects due to a direct interaction with GABA-A receptors. PRO is mainly excreted in the urine, although a significant pulmonary uptake and first-pass elimination have been r

The use of suitable therapeutic protocols is particularly important when extra-label drugs are used or when physiological parameters are modified, as in the case of the administration of alkaline substances to racehorses. The pharmacokinetics of naproxen (NAP), after both ...