Forty two small ruminants, 26 (61.90%) sheep and 16 (38.10%) goats were treated for rumen ACIDOSIS. 19 (45.24%), 12 (28.57%), 6 (14.29%) and 5 (11.90%) animals had eaten apple, cooked rice (wazwan left over) turnip and chapatti respectively and manifested clinical form of ruminal ACIDOSIS with, 2.86%; (n=18) as mild (Rumen fluid pH=6.32 ±0.09316), 38.09%; (n=16) moderate (Rumen fluid pH=5.71 ±0.074) and 19.05%; (n=8) (Rumen fluid pH=4.54 ±0.159) as severe ruminal ACIDOSIS and accordingly they were classified as group I, II and III, respectively. In group I rumen motility was reduced (1.67±0.162) and subsequently it was almost absent in group III (0.13±0.125). Rectal temperature recorded to be 102.58±0.166, 101.26±0.188 and 100.83±1.061 in group I, II and III respectively. There was a significant increase heart and respiratory tares before treatment in all the groups. A significant increase in blood glucose and Hb, PCV and TEC was also observed in mild, moderate and severe acidotic animals. Therapeutic measures consisted of neutralization of acidity by oral and / or parenteral use of isotonic (1.3%) and hypertonic (5%) sodium bicarbonate with adequate fluid therapy. Oral and parenteral use of isotonic (1.3%) sodium bicarbonate was given to moderate rumen ACIDOSIS. Administration of oral sodium bicarbonate, bolus Rumentas was given to groups I and II and a course of antihistaminic drug was also given to all the groups of animals. Moreover, animals of group II and III were also offered intravenous injection of high dose vitamin B1 along with fluids. Gastric lavage and cud transplantation following rumenotomy was done in animals of group III. All animals except two (one each from group II and III) were recovered uneventfully.

Background: Mitochondrial myopathy, encephalopathy, lactic ACIDOSIS and stroke-like episodes (MELAS) is a progressive maternally inherited multi-organ disorder caused by a mutation in a mitochondrial gene. In this disorder recurrent migraine headache, seizure, cerebral insults causing hemiparesis, hemianopia, progressive hearing loss and cognitive problems may occur.Case presentation: The patient is a 12-year girl manifested with malaise, tonic-clonic convulsion and unilateral weakness in left upper and lower extremities. Her problem was begun with seizure, headache and recurrent vomiting, 5 months before the admission. On clinical examination cerebrovascular events was diagnosed. On broader diagnostic studies, also a genetic mutation in A3243G gene, as a definite characteristic for the establishment of the disease, was detected by muscle biopsy.Conclusion: Patients suffering from the syndrome gradually display delayed motor and cognitive development. Therapeutic management of the disease consists of administration of multi-vitamins and coenzyme supplementations, and lowering the serum lactate level using dichloroacetate.

For induction of ruminal ACIDOSIS, 10 clinically healthy three years old non pregnant female sheep were selected. Prior to the infusion of sucrose (0 hour), rumen and blood samples were obtained in order to determine baseline rumen and blood pH, respectively. Electrocardiogram (ECG) was also recorded. Acute ruminal ACIDOSIS was induced experimentally with sucrose at a dose of 18g kg-1 body weigh through rumen fistula. ECG was recorded and blood and rumen samples collected at 3, 6, 9, 12, 15, 18, 21, 24, 30, 36, and 48 hours after the infusion of sucrose. Results indicated that blood and rumen pH decreased significantly at 15, 18, 21, 24, 30, 36 and 48 hours and at 3, 6, 9, 12, 15, 18, 21, 24, 30, 36 and 48 hours, respectively. ACIDOSIS produced a marked increasing in heart rate and a decrease in PR interval at 15 and 18 hour significantly with little apparent effect on the ST and PR segment. The P amplitude increased significantly at 6, 9, 12, 15, 18, 21, 24 and 30 hours. The T amplitude increased significantly at 9, 12, 15, 18, 21, 24, 30 and 36 hours. The RR interval decreased significantly at 6, 9, 12, 15, 18, 21, 24, 30, 36 and 48 hours. In conclusion acute ruminal ACIDOSIS caused significant changes in ECG of sheep though there was not any detectable arrhythmia in the ECG in acute ruminal ACIDOSIS.

A case of renal tubular ACIDOSIS (RTA) who had gradual onset of paralysis of lower extremities and persisted for a long time is presented. His primary workups were mistaken for muscular dystrophy. Eventually, an abdominal ultrasonography revealed small stones in both of the kidneys and his workup for the stones were in favour of distal renal tubular ACIDOSIS and advanced rickets with hypokalemia. He had a dramatic response to alkaline therapy. There are many reports of periodic paralysis in RTA but no report of prolonged paralysis is found in the literature.