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Serum creatinine was measured in 1996 1997 (baseline) with the Kodak Ektachem 700 Analyzer (Eastman Kodak, Rochester, NY), which uses a colorimetric method.
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Total flavonoids content was determined using a colorimetric method as described by Heimler et al. [26].
DPPH was determined using a colorimetric method as described by Chen and Ho [29].
Condensed tannin content was determined using a colorimetric method as described by Broadhurst and Jones [27].
The total flavonoid concentration was determined by using a colorimetric method with minor modification (Bao et al. 2005).
Ferric reducing antioxidant capacity (FRAP) was determined using a colorimetric method as described by Benzie and Strain [30].
Total phenolic content was determined using a colorimetric method as described by Singleton et al. [24, 25].
ABTS was determined using a colorimetric method as described by Brown and Miller [31], and Re et al. [32].
TCC was determined using a colorimetric method as described by Sanusi and Adebiyi [33], with slight modifications.
The ability of our synthetic compounds to inhibit ovine COX-1 and COX-2 was determined using a colorimetric method.
Phytase production was measured using a colorimetric method by following the release of inorganic phosphate from phytic acid according to the method presented by Dhiman et al. (2002).
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