2% (w/v) Taro |
Growth and adherence of Lactobacillus species (in vitro) |
Improvement of human gut microbiota through prebiotic potential of taro |
↑ growth of L. acidophilus, L. paracasei, and L. plantarum ↑ self‐agglutination of L. paracasei
|
Saxby et al. (2019) |
Aqueous extract of taro |
Streptococcus mutans
|
Antimicrobial activity |
↓ growth |
Singh et al., (2012) |
Ethanolic extract of taro |
Alloxan‐induced diabetic mice |
Antihyperglycemic effect |
Reduced glycemic activity |
Singh et al.(2012) |
Extract of taro 400 mg/kg bw |
Male Sprague Dawley rats |
Antidiabetic and antianemic effect |
Inhibited aldose reductase enzyme activity, increased production of hemoglobin |
Sulistiani et al. (2020) |
Ethanolic leaves concentrate |
Wister rats, granuloma model |
Anti‐inflammatory activity |
Calmed the inflammation |
Keerthy and Joshi (2019) |
Ethanolic and aqueous extract produced five digalactosyl‐diacylglycerols (DGDG) and three monogalactosyl‐diacylglycerols (MGDG) |
Human Caco cell lines |
Anticholesterol synthesis, declined cholesterol‐induced colorectal cancer (CRC) |
Inhibition of human lanosterol synthase (hOSC), declining risk of CRC |
|
Ethanolic taro leaf extracts 10–50 mg/mL |
Earth worms |
In vitro anthelmintic activity |
Potent paralysis and death time |
Kubde et al. (2010) |
25% Alcoholic concentration of taro leaf extract |
Alternaria ricini and Alternaria solani
|
In vitro antifungal activity |
Inhibition of pathogenic growth |
Mengane (2015) |
Taro leaf juice |
In vitro rat liver slice model |
Hepatotoxins (CCl4 and acetaminophen) induced lipid peroxidative reactions |
Prevented the elicit of these reactions and protected liver |
Patil and Ageely (2011) |