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. 2019 Oct 22;8(10):504. doi: 10.3390/antiox8100504

Table 1.

Design of the experimental study groups.

Day 1 2 3 4 5 6 7 7 (i.p.) 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 22 (s.c.)
Group
N-C saline by gavage CB saline by gavage SS
AMI-C CB ISO
DM-C STZ SS
DM-AMI-C STZ ISO
S-DM-CUS-AMI STZ CUS by gavage ISO
CUS-DM-CUS-AMI CUS by gavage STZ ISO
S-DM-CUN-AMI saline by gavage STZ CUN by gavage ISO
CUN-DM-CUN-AMI CUN by gavage STZ ISO

Notes: N, normal; C, control; AMI, acute myocardial infarction; DM, diabetes mellitus; SS, saline solution (0.09%); CB, citrate buffer; CUS, curcumin solution (200 mg/kg bw); CUN, curcumin nanoparticle solution (200mg/kg bw); STZ, streptozotocin in a dose of 65 mg/kg bw; ISO, isoproterenol in a dose of 45 mg/kg bw; i.p., intraperitoneal; s.c., subcutaneous.