ABSTRACT
Background: There has been enormous curiosity in the development of alternative plant based medicinesto control diabetes, oxidative stress and related disorders. One of the therapeutic approaches is to reducepostprandial release of glucose in the blood. Two key enzymes that are involved in reducing postprandialglucose are a-amylase and a-glucosidase. Mentha arvensis L. has been traditionally used by several tribesas a medicinal plant to treat various disorders.Objective: The present study was undertaken to test M. arvenisis L. for inhibition of postprandialhyperglycemia.Material and method: We performed various in vitro and in vivo tests to evaluate efficacy of M. arvenisis L.for antidiabetic activity (postprandial hyperglycemia).Results: Methanolic extract of M. arvensis L. leaves showed DPPH free radical scavenging activity (morethan 78% mg/ml) and high antiglycation potential (more than 90% inhibition of AGE formation). Methanolic extract also showed remarkable inhibitory effects on a-amylase (more than 50% mg/ml) and aglucosidase (68% mg/ml) and significant inhibition of postprandial hyperglycemia in starch induced diabetic Wistar rats.Conclusion: The non-insulin dependent antidiabetic or inhibition of postprandial hyperglycemic activityof methanolic extract of M. arvensis L. leaves was shown by using in vitro and in vivo approaches in thepresent study.© 2018 Transdisciplinary University, Bangalore and World Ayurveda Foundation. Publishing Services byElsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
ABSTRACT
Background: Urolithiasis is the third common disorder of the urinary system affecting 10e15% of thegeneral population. In recent years, search for new antilithiatic drugs from natural sources has assumedgreater importance.Objectives: This study was performed to investigate the anti-urolithiatic activity of methanolic extract ofDuranta erecta leaves by in vitro and in vivo analysis.Materials and methods: The study was designed to determine presence of phytochemicals in D. erecta, itsyield in percentage, antioxidant activity against 2, 2-diphenyl-1-picrylhydrazyl (DPPH) and anti-microbial property against few bacteria. In vitro analysis was carried out study anti-urolithiatic property ofD. erecta by nucleation assay and synthetic urine assay for inhibition of calcium oxalate and calciumoxalate monohydrate crystals formation. An in vivo experiment was performed on Wistar rats forconfirmation of anti-urolithiatic property of D. erecta in animal model.Results: D. erecta has the presence of primary and secondary metabolites like glycoside, saponins, sterols,flavonoids, phenols, tannins, alkaloids, carbohydrates and proteins. Methanolic extract of D. erecta gave avery good yield (60%). D. erecta proved its antioxidant potential by 93.51% inhibition of DPPH radical at aconcentration of 1000 mg/mL where ascorbic showed 94.71% of DPPH radical at the same concentration.In vitro tests like nucleation assay and synthetic urine assay showed that D. erecta inhibits formation ofcalcium oxalate and calcium oxalate monohydrate crystals. It also showed the anti-microbial property byformation of zone of inhibition against few bacteria. An in vivo experiment on Wistar rat animal modelconfirmed the anti-urolithiatic property of D. erecta L. leaves extract.Conclusions: Based on the results, we reported that D. erecta may treat calcium oxalate crystal depositionin the kidney by preventing hyperoxaluria-induced peroxidative damage to the renal tubular membranesurface (lipid peroxidation). It has anti-microbial potential so it may also inhibit the secondary bacterialinfection in kidney. Based on the data, it can be concluded that this herb can be used as a potential antiurolithiasis agent for kidney stone removal.© 2017 Transdisciplinary University, Bangalore and World Ayurveda Foundation. Publishing Services byElsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
ABSTRACT
Approximately 52% of the nuclear genome of great millet (Sorghum vulgare) consists of repetitive DNA which can be grouped into very fast, fast and slow components. The reiteration frequencies of the fast and slow reassociating components are 7000 and 92 respectively. Approximately 90% of the genome consists of repeated sequences interspersed amongst themselves and with single copy sequences. The interspersed repeat sequences are of three sizes viz. > 1·5 kilobase pairs, 0·5–1·0 kilobase pairs and 0·15–0·30 kilobase pairs while the size of the single copy sequences is 3·0 kilobase pairs. Hence the genome organization of great millet is essentially of a mixed type.
ABSTRACT
Approximately 39 to 49% of the genome of finger millet consists of repetitive DNA sequences which intersperse with 18% of single copy DNA sequences of 1900 nucleotide pairs. Agarose gel filtration and electrophoresis experiments have yielded the sizes of interspersed repeated sequences as 4000-4200 nucleotide pairs and 150-200 nucleotide pairs. Approximately 20% of the repeated DNA sequences (4000-4200 nucleotide pairs) are involved in long range interspersion pattern, while 60% of the repeated DNA sequences (150-200 nucleotide pairs) are involved in short period interspersion pattern. Based on the data available in literature and the results described here on DNA sequence organization in plants, it is proposed that plants with haploid DNA content of more than 2.5 pg exhibit mostly the short period interspersion pattern, while those with haploid DNA content of less than 2.5 pg show diverse patterns of genome organization.