There is little information known about the energy requirements of cats in temperature climates. Energy requirement of domestic short-haired cats was determined using three groups of mixed gender - old kept outside (approximately 9.9 years of age; 4.8 kg; n = 9), young kept outside (approximately 3.1 years of age; 3.9 kg; n = 8) or young kept inside (approximately 3.1 years of age; 3.9 kg; n = 8). Cats were housed individually for 5 weeks during summer (18.5 ± 0.5 °C) and winter (8.5 ± 0.4 °C) and were fed a commercially available maintenance diet ad libitum. In both periods, energy expenditure was determined from the rates of (2) H and (18) O elimination for blood H2 O over a 12 day period, from a doubly labelled water bolus (2) H2 O (0.7 g/kg BW) and H2 (18) O (0.13 g/kg BW) administered intravenously. During the summer period, macronutrient digestibility was determined. Older cats had a reduction (p < 0.05) in apparent digestibility of dry matter (approximately 9%), energy (approximately 8%) and protein (6%). There was a significant effect of age and season on energy intake and energy expenditure. While lean mass was affected by age and season, there was no effect of age or season on energy expenditure when expressed as a proportion of lean mass. Possible seasonal differences in nutrient digestibility may explain these results.

Obesity is highly prevalent in pet cats (Felis silvestris catus) and is associated with several comorbidities, yet very little is understood about the early life risk factors. The aim of this study was to develop a mathematical model that describes growth in cats, to determine which early life variables were associated with being overweight in adulthood and to identify when during life the overweight phenotype developed in a colony of cats. We used pedigree, birth and growth data of 212 colony cats that were fed ad libitum from weaning. A nonlinear mixed-effects model was fitted to the body weight data to describe growth curves. A subset of 146 cats that had reached 9 years of age was used to evaluate the body weight curves to 9 years, and candidate early life predictors of peak weight were evaluated using logistic regression. In contrast with other species, candidates such as maternal factors, birth weight and litter size were not significant risk factors for adult obesity. Male sex, body weight around 15 weeks of age and being born during the increasing photoperiod were significantly associated with being overweight at 9 years. The growth equation created can be used to predict peak body weight, when sex and season of birth are included. Thus, the trajectory to obesity is determined early in life in cats, and early intervention appears essential to prevent obesity in pet cats.

Two days after castration, urinary free felinine plus N-acetylfelinine decreased 24% in male cats, but, by day 5, the concentration had not decreased to that routinely found in males that have been castrated for several months. In a second experiment, three groups of castrated adult male cats received different subcutaneous injections: control (carrier), testosterone, testosterone plus estradiol. A fourth group of intact adult female cats received a testosterone injection. Urine was collected and analysed for free felinine, N-acetylfelinine and 3-methylbutanolglutathione. Baseline blood testosterone and estradiol concentrations were low during the pre-period, but increased sharply after hormone injections. The concentration of all three urinary metabolites increased as a result of testosterone injections with estradiol not modulating the effect. The effect of testosterone was not gender dependent. The concentration of free felinine, N-acetylfelinine and 3-methylbutanolglutathione in the urine remained low in the placebo control group throughout the study. The relative molar contribution of free felinine to the total amount of felinine containing compounds increased due to testosterone treatment, while the contribution of 3-methylbutanolglutathione and N-acetylfelinine decreased. Testosterone increases free felinine, N-acetylfelinine and 3-methylbutanolglutathione excretion in castrated adult male and intact female cats, whereas estradiol does not modulate this effect.

Felinine is a branched-chain sulfur amino acid present in the urine of certain Felidae, including domestic cats. The objective of the present study was to determine if additional cystine and/or dietary N would increase felinine and N-acetylfelinine excretion by intact male cats fed a low-protein (LP) diet. Feeding five adult intact male cats an LP diet (18·8 % of metabolisable energy (ME) as protein) v. a high-protein diet (38·6 % of ME as protein) resulted in a trend (P¼ 0·08) for decreased urinary felinine and no change in N-acetylfelinine excretion. In a 23 d study, when the LP diet was supplemented with L-cystine at 9·3 g/kg DM, urinary felinine:creatinine ratio showed a linear two-fold (121 %) increase (P,0·01) from 0·24 (SEM 0·05) to 0·53 (SEM 0·13) after 10 d. Subsequent feeding of the LP diet resulted in a decrease in felinine excretion to base levels. Plasma gglutamylfelinylglycine concentrations were consistent with the excretion of felinine. Supplementation of the LP diet with L-cystine (9·3 g/kg DM), dispensable amino acids and arginine to a second group (n 5) also resulted in a significant (P,0·01) but smaller (þ 72 %) increase in the daily felinine:creatinine ratio (0·25 (SEM 0·04) to 0·43 (SEM 0·05)). The degree of felinine N-acetylation within groups was unaffected by dietary addition and withdrawal of amino acids. The results indicate that felinine synthesis is regulated by cystine availability, and that arginine may be physiologically important in decreasing felinine biosynthesis in intact male cats. N-acetylfelinine: Arginine: Cats: Cysteine: FelinineFelinine is a unique amino acid excreted by certain species within the Felidae family, including the domestic cat. This sulfur-containing, branched-chain amino acid has been found in concentrations of 3·6 g/l in the urine of intact male cats (Felis catus), with castrated males excreting approximately one-quarter as much as intact males (1) . Synthesis of felinine is believed to occur from glutathione and isopentenylpyrophosphate, through a unique glutathione sulfur transferase enzyme which is under hormonal control (2,3) to form a felinine-containing tripeptide: g-glutamylfelinylglycine or methylbutanolglutathione (MBG). The g-glutamylfelinylglycine is transported in the blood (4) to the kidney where hydrolysis by g-glutamyltransferase present on the surface of the brushborder membrane of proximate tubular cells results in felinylglycine and glutamic acid. The dipeptide can be further hydrolysed to felinine and glycine by either dipeptidase activities or a recently discovered enzyme with carboxylesterase activity (5) . This 70 kDa enzyme (cauxin) has been found in relatively high concentrations in feline urine and has been shown to be able to hydrolyse felinylglycine but not MBG (5) . Following the hydrolysis of felinylglycine, N-acetylation of felinine can occur. This is an intracellular process catalysed by cysteine-S-conjugate N-acetyltransferase and yielding mercapturic acids via the addition of an acetyl group transferred from acetyl-CoA, whi...

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