1) Numerous studies on diabetogenic action of organic reagents have been made since discovery of the oxine and dithizone diabetes. But, it is necessary to find other active agents and to examin their action precisely in order to reneal the acting mechanis of these diabetogenic agents.
Therefore, present studies on diabetogenic action and histological changes in islet of Langerhans in rabbits caused by potassium ethylxanthate and quinoline derinatines have been under taken.
2) All rabbits injected with potassium ethylxanthate showed initial hyperglycemia and subsequent hypoglycemia in 50 persent, from which they are irreconerable despite of administrating glucose and epinephrine.
About thirty per cent of rabbits, which did not show marked hypoglycemia, then, showed diabetic state after forty-eight hours.
By repeated daily injection from four to twenty times of potassium ethylxanthate, slight hyperglycemia and diabetic state were observed.
By injection of potassium ethylxanthate, a alloxan-diabetic rabbit died from hypoglycemia after 3 days.
3) Out of thirteen quinoline derivationes, 5 aminooxine and 8-hydroxy quinaldine were observed to cause marked changes in blood sugar with dostruction of islet of Langerhans.
By 5 aminooxine initial hyperglycemia followed by subsequent hypoglycemia or normal lenel of blood sugar and then diabetic state were observed from 48 hours to 5-7 days.
By 8-hydroxy-quinaldine initial hyperglycemia followed by slight hypoglycemia and secorndary hyperglycemia, permanent diabetes were noted.
4) Histological studies of rabbit injected with 5-aminooxine and 8-hydroxy quinoline could reneal remarkable changes in islets of Langerhans in pankreas.
Degenerative changes of beta cells of islets in early stage and senere necrosis and disintegration in hypoglyceinie stage were observed.
In diabetic stadium, islets were reduced in number and size and were chiefly composed of alpha cells.
In rabbits in hypoglycemic state caused by potassium ethylxanthate, degenerative changes in nerve cell in brain were observed. No remarkoble damages were noted in other tissues.
5) Histochemical study demonstrated no glycogen in tissues from hypoglycemic animals.
6) Close correlation between diabetogenic action and chemical stuructures were established in quinoline derivatives.
A Hydroxy group in position 8 of quinoline was essential for destructing action on islet tissues.
Increase of hydroxy and carboxyl groups dimishen their toxicity remarkably and abolished the specific action despite of hydroxy group in position 8.
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