SUMMARY1. Under fluothane anaesthesia, suction decerebration was performed at the immediate pre-pontine level in adult, male, Sprague-Dawley rats; this resulted in a large and sustained rise in rectal temperature from 35-6 ± 0-2 (control) to 38-8 + 0.5 0C (decerebrate) following recovery from anaesthesia. Propranolol inhibited this rise.2. In a separate group of continuously (urethane) anaesthetized rats, brain transaction at the immediate pre-pontine level produced marked increases in rectal temperature and oxygen consumption, both of which were inhibited by injection of the fl-adrenergic antagonist propranolol (10 mg/kg).3. The rise in rectal temperature (2-8 ± 0-4 'C) after transaction was preceded by a greater increase (3-6 ± 0 3 'C) in the temperature of the interscapular brown adipose tissue (i.b.a.t.). Skin temperature on the tail showed no immediate response.4. In anaesthetized lean (+ / ?) male Zucker rats, rectal and i.b.a.t. temperatures showed similar responses to Sprague-Dawley rats after decerebration, but in the genetically obese (fa/fa) Zucker rat, temperatures were not significantly altered by decerebration.5. The above results, together with macroscopic examination of the transacted brains, suggest that descending pathways (possibly arising in the mid-brain tegmentum) normally inhibit a sustained thermogenic drive from areas in the lower brain stem. Decerebration can release this inhibition and cause a large rise in body temperature and in metabolic rate, which apparently result from sympathetic activation ofi.b.a.t. The genetically obese Zucker rat exhibits an impaired thermogenic response to decerebration.