Two ponies presented with mild abdominal pain and mild
diarrhoea one hour after ingestion of roots of a black locust
tree. On admission, symptoms had progressed to
depression, weakness and the passing of dark, firm faeces.
Treatment was symptomatic and supportive, aiming at the
evacuation of the toxin from the gastrointestinal tract. One
pony developed severe, reversible neurological signs
associated with transient hyperammonaemia in the
absence of liver disease. After 24 h the ammonia level
returned to normal and central nervous signs disappeared.
Both ponies recovered completely. This report describes
the ingestion of black locust closely followed by
the development of central nervous signs and
hyperammonaemia. Increased ammonia absorption due
to the intestinal wall inflammation caused by the toxins of
the black locust tree, as well as increased ammonia
production by enteric bacteria is therefore considered
a plausible pathophysiological mechanism of the
neurological signs displayed in black locust intoxicatio