Blood lactate disappearance after maximal exercise in trained and detrained horses

The influence of training on blood lactate concentrations during treadmill exercise and a 40-minute inactive recovery period was examined in seven trained and seven detrained thorough-bred horses. Lactate concentrations were measured in venous blood collected at the end of each exercise state, and at intervals for 40 minutes afterwards. Measurements were made of maximum oxygen uptake (V̇O_2max, ml kg⁻¹ min⁻¹), VLA4 (velocity at which blood lactate concentration was 4 mmol litre⁻¹); LA8 (lactate concentration [mmol litre⁻¹] during exercise at 8 m sec⁻¹), peak lactate (highest lactate concentration after exercise), LA40 (lactate concentration 40 minutes after exercise), the time of peak lactate concentration (minutes after exercise) and the rate of disappearance of blood lactate (Rt_d). The trained horses had a significantly lower LA8 (2·1 ± 0·1 vs 6·5 ± 1 mmol litre⁻¹, P<0·01), higher VLA4 (9·8 ± 0·2 vs 5·8 ± 0·6 m sec⁻¹, P<0·01) and higher V̇0_2max (156·3 ± 3·8 vs 107·1 ± 3·9 ml kg⁻¹ min⁻¹, P<0·001). The value of Rt_d and the time of peak lactate concentration were not significantly different.     

Mixed function oxidase and glutathione transferase activity in last instar Heliothis virescens larvae

Methyl parathion-resistant and -susceptible strains of Heliothis virescens were assayed for mixed function oxidase and glutathione transferase activity at four time periods within the last instar. No significant differences were found between the mixed function oxidase or glutathione transferase activities of the resistant and susceptible strains. However, significant differences did appear among time periods within the last instar. Larvae assayed during the postfeeding time period (60–80 hr) had the highest mixed function oxidase activity, which was 28 times that of last instar larvae assayed during the first time period (0–19 hr). Glutathione transferase activity appeared to be highest during the 20- to 39-hr and 40- to 59-hr time periods, but the differences among time periods were small. The importance of these findings to studies of insecticide resistance and plant herbivore interactions is discussed.     

Endogenous inhibitors of glutathione S-transferases in house flies

The inhibition of glutathione S-transferase by endogenous compounds present in the soluble fraction of house fly homogenates was investigated. The highest inhibition was found with the female abdomen and increased with incubation time and with an increase in the tissue concentration. The correlation of increased inhibition with a parallel increase in the darkening of the soluble fraction indicated a possible association with melanization, thereby suggesting quinones as the possible endogenous inhibitiors of glutathione transferase. In vitro experiments demonstrated that quinones produced by mushroom tyrosinase did indeed inhibit glutathione S-transferase. Inhibition by quinones can be prevented by including glutathione or bovine serum albumin in the homogenization buffer. The inhibitory activity of a variety of quinones and related compounds on purified glutathione S-transferase was investigated. Oxygenated aromatics with hydroxy groups in the 1,2- or 1,4-position or ketonic carbonyls in the 1,4-position are good inhibitors of glutathione S-transferase.     

The development of flamprop-isopropyl—A new wild oat herbicide for use in barley

Flamprop-isopropyl, isopropyl (±)-2-[N-(3-chloro-4-fluorophenyl)benzamido]-propionate, has been shown to give good control of Avena spp. in barley. Results from glasshouse tests have been confirmed in field trials over two seasons, in 8 European countries, using a 200 g/litre formulation of the herbicide. In Spring barley the crop stage during which application should be made for optimum weed control and crop benefit lies between late tillering and the formation of the second node.     

Toxicological studies with the 1,3,5-triazine herbicide cyanazine

Acute and long-term mammalian toxicity studies were carried out with the 1,3,5-triazine herbicide cyanazine (I) and its two major plant and soil metabolites DW 43 85 (II) and DW 4394 (III). Depending upon the species used, the acute oral LD50 values for cyanazine ranged from 140-750 mg/kg, the values in any one species not being influenced by formulation. The acute, percutaneous LD50 values were greater than 1000 mg/kg, the maximum dose which could be administered. Cyanazine was non-irritant to eyes and skin and a non-sensitiser to skin. The acute oral LD50 in rats for (II) was 789 mg/kg and for (III) was >2000 mg/kg. In 13-week studies on cyanazine, reduced growth rates and organ weight changes were the most sensitive criteria of exposure, 25 parts/million in the diet of rats and 5 mg/kg orally dosed to dogs being considered to be without toxicological effect. In two year studies 12 parts/million in the diet of rats and 1.25 mg/kg, orally dosed to dogs produced no changes of toxicological significance. In 13-week studies with (II) and (III), intakes of up to 10 000 parts/million in the diet failed to produce any toxicologically significant changes.     

Sodium monofluoroacetate (Compound 1080) poisoning in dogs

Sodium monofluoroacetate (Compound 1080) is a widely used pesticide for control of feral animals such as the fox. Accidental poisoning of domestic animals occurs despite strict regulations on 1080 usage. Dogs are particularly susceptible to the toxin. The mechanism of 1080 toxicity, susceptibility of target and non-target species, persistence of 1080 in the environment and risk of accidental poisoning are discussed. Particular emphasis is placed on 1080 toxicity in the dog. Early recognition of intoxication is most important for prognosis and relies upon characteristic clinical signs and diagnostic findings. The treatment of 1080 intoxication remains a challenge with no proven antidotes. However, there are possible benefits from monoacetin, acetamide, calcium salts, colestipol, activated charcoal, peritoneal dialysis, sodium bicarbonate, neurotransmitter modulators and four-methylpyrazole. A recommended treatment protocol for 1080 toxicosis in dogs is included. Safety measures such as the use of wire dog muzzles and investigating alternatives to 1080 in pest control programs may be the key to reducing the incidence of future accidental poisonings.     

Management of equine sarcoids: 1975-93

Treatment options for equine sarcoids are briefly reviewed and the results of a retrospective study of 63 cases of equine sarcoid (66 lesions) treated by clinicians from the Rural Veterinary Centre, Camden, Australia from 1975 to 1993 presented. Five different treatments were employed in the management of these 66 lesions, including surgical excision alone or in combination with cryotherapy, radiotherapy, immunotherapy and tumour transfer to a subcutaneous site on the neck. The majority of cases were treated with surgical excision alone (18/66), excision followed by cryotherapy (31/66) and immunotherapy (16/66), with success rates of 28%, 42% and 81% respectively. Success was defined as no sign of recurrence of the lesion at the time of follow-up, at least 6 months later.