TY - JOUR
T1 - Antidiabetic effect through islet cell protection in streptozotocin diabetes
T2 - A preliminary assessment of two thiazolidin-4-ones in Swiss albino mice
AU - Kishore, Anoop
AU - Nampurath, Gopalan Kutty
AU - Mathew, Suma P.
AU - Zachariah, Robby T.
AU - Potu, Bhagath Kumar
AU - Rao, Muddanna S.
AU - Valiathan, Manna
AU - Chamallamudi, Mallikarjuna Rao
PY - 2009/2/12
Y1 - 2009/2/12
N2 - This study was undertaken on the basis of several reports in the literature that pancreatic beta cells are capable of replication/regeneration and also being afforded protection against damage induced by streptozotocin. Nicotinamide was reported to give protection against streptozotocin-induced damage in rats. In the present study, two thiazolidine-4-ones with nicotinamide substitution were administered to Swiss albino mice with streptozotocin diabetes for 15 days. Concurrently, one group received nicotinic acid. Both the test compounds reversed the hyperglycaemia diabetic mice. Damage to pancreatic islets was also reduced in these groups compared to diabetic control and nicotinic acid treated groups. Since these compounds have been earlier found have antioxidant activity, one of the possible mechanisms of action could be by reducing oxidative stress in pancreas. Further, possibly by releasing nicotinamide in vivo, the molecules could have contributed to the NAD pool in pancreas and afforded protection. It is concluded that the test compounds have potential to be developed for multiple beneficial action in conditions like metabolic syndrome.
AB - This study was undertaken on the basis of several reports in the literature that pancreatic beta cells are capable of replication/regeneration and also being afforded protection against damage induced by streptozotocin. Nicotinamide was reported to give protection against streptozotocin-induced damage in rats. In the present study, two thiazolidine-4-ones with nicotinamide substitution were administered to Swiss albino mice with streptozotocin diabetes for 15 days. Concurrently, one group received nicotinic acid. Both the test compounds reversed the hyperglycaemia diabetic mice. Damage to pancreatic islets was also reduced in these groups compared to diabetic control and nicotinic acid treated groups. Since these compounds have been earlier found have antioxidant activity, one of the possible mechanisms of action could be by reducing oxidative stress in pancreas. Further, possibly by releasing nicotinamide in vivo, the molecules could have contributed to the NAD pool in pancreas and afforded protection. It is concluded that the test compounds have potential to be developed for multiple beneficial action in conditions like metabolic syndrome.
UR - http://www.scopus.com/inward/record.url?scp=58349108316&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=58349108316&partnerID=8YFLogxK
U2 - 10.1016/j.cbi.2008.10.032
DO - 10.1016/j.cbi.2008.10.032
M3 - Article
C2 - 19038238
AN - SCOPUS:58349108316
SN - 0009-2797
VL - 177
SP - 242
EP - 246
JO - Chemico-Biological Interactions
JF - Chemico-Biological Interactions
IS - 3
ER -