2018
DOI: 10.1007/s13205-018-1156-8
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Evidence of antidiabetic activity of Spirulina fusiformis against streptozotocin-induced diabetic Wistar albino rats

Abstract: The aim of our study is to investigate the protective effect of against streptozotocin-induced diabetes inWistar albino rats. Rats were divided into five groups: group I was normal control, group II was diabetic control (50 mg/kg b.w. of streptozotocin, i.p.), group III was (400 mg/kg b.w., p.o.) treated diabetic rats; group IV was Glibenclamide (0. 6 mg/kg b.w., p.o.) treated diabetic rats and group V was treated with (400 mg/kg b.w., p.o.) alone. There was significant elevation in the levels of blood glucose… Show more

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Cited by 21 publications
(21 citation statements)
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“…The presence of methoxy group in aromatic ring of compound (5) was supported by the appearance of sharp singlet at δ 3.81 (ppm) in the 1 H-NMR spectrum. 13 C-NMR spectrum confirmed the addition of carbon at δ (ppm) 60.8 that showed addition of methoxy group in compound (5). Furthermore, the molecular weight of compound (5) was found to be appropriate with the target structures.…”
Section: Compound (3)mentioning
confidence: 73%
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“…The presence of methoxy group in aromatic ring of compound (5) was supported by the appearance of sharp singlet at δ 3.81 (ppm) in the 1 H-NMR spectrum. 13 C-NMR spectrum confirmed the addition of carbon at δ (ppm) 60.8 that showed addition of methoxy group in compound (5). Furthermore, the molecular weight of compound (5) was found to be appropriate with the target structures.…”
Section: Compound (3)mentioning
confidence: 73%
“…1 H NMR (proton NMR) was identified using JEOL JNM-ECP (500 Hz) in CDCl 3 as solvent. 13 C NMR (carbon NMR) was identified using JEOL JNM-ECP (125 Hz) in CDCl 3 as solvent. The measurement results are known from the difference of the chemical shifts which expressed in ppm and coupling constants are measured in Hertz (Hz).…”
Section: Synthesis Reactionmentioning
confidence: 99%
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