The vehicle was administered in the same manner. Fifteen beagle dogs were allocated on restricted randomization based on weight and sex to form 5 equal groups of 3 dogs each. Those groups were allocated randomly to treatment. The treatment groups were: 0 mg/kg fed, 1.5 mg/kg fed, 2.5 mg/kg fed, 2.5 mg/kg fasted and 3.5 mg/kg fed. In the fed group, food was given prior to dosing whereas in the fasted group food was removed the night prior to dosing and not returned until 2 h post-dosing. Flea and tick challenges were conducted at periodic JAK drugs intervals over the course of one month. Blood samples were taken at least weekly for the duration of the study. Afoxolaner was prepared for a dosage of 2.5 mg/kg

to be administered five times orally at 30 days intervals at the rate of 0.2 ml/kg dog weight. The vehicle was administered in the same manner. Six beagles were allocated randomly to the 2.5 mg/kg treatment and six beagles were allocated to treatment with vehicle only. Flea and tick challenges were made every week over the course of five months, with counts conducted at appropriate intervals after each challenge. Blood samples were taken VX-770 solubility dmso at least weekly for the duration of the study. Dog weights were measured on Day

1, and then on Days 7, 14, and 29 of each monthly dosing cycle. Final weights were collected on Day 31 after the fifth dose. At each dosing, dogs were observed at 30 min, 2 and 4 h post dosing, and daily for the duration of the study (150 days). Each dog had a physical examination by a veterinarian at Day 1, and then on Days 1, 14 and 29 of each monthly dosing cycle. Initial mode of action studies were conducted using the related isoxazoline, CPD I, with more detailed studies during conducted using afoxolaner (Fig. 1). Adult male American cockroaches (Periplaneta americana), were injected with 0.1–10 μg CPD I through the ventral intersegmental membrane of the abdomen with appropriate concentrations of CPD1 dissolved in 2 μL DMSO. Observations

of insect toxicity and mortality were conducted over a 72 h period and a KD50 (50% knockdown concentration) was calculated. To aid in elucidating the target site of isoxazoline insecticides, activity of CPD I was investigated on an in vitro preparation. Cockroaches possess an escape reflex circuit (cercal reflex) in which mechanical stimulation of hairs of the cerci produce bursts of action potential spikes which travel through the ventral nerve cord in an anterior direction producing excitation of motor nerves ( Fig. 4a). Nerve conduction for this reflex circuit involves the excitatory and inhibitory neurotransmitter receptors, acetylcholine and GABA, respectively, as well as voltage-gated sodium and potassium channels. Extracellular recordings were conducted on nerve 5 (N5) of the metathoracic ganglion of American cockroaches.