Progressive hemorrhage and myotoxicity induced by echis carinatus venom in murine model: neutralization by inhibitor cocktail of n,n,n `,n `-tetrakis (2-pyridylmethyl) ethane-1,2-diamine and silymarin

Viperbite is often associated with severe local toxicity, including progressive hemorrhage and myotoxicity, persistent even after the administration of anti-snake venom (ASV). In the recent past, investigations have revealed the orchestrated actions of Zn2+ metalloproteases (Zn(2+)MPs), phospholipase A(2)s (PLA(2)s) and hyaluronidases (HYs) in the onset and progression of local toxicity from the bitten site. As a consequence, venom researchers and medical practitioners are in deliberate quest of potent molecules alongside ASV to tackle the brutal local manifestations induced by aforesaid venom toxins. Based on these facts, we have demonstrated the protective efficacy of inhibitor cocktail containing equal ratios of N,N,N', N'-tetrakis (2-pyridylmethyl) ethane-1,2-diamine (TPEN) and silymarin (SLN) against progressive local toxicity induced by Echis carinatus venom (ECV). In our previous study we have shown the inhibitory potentials of TPEN towards Zn(2+)MPs of ECV (IC50: 6.7 mu M). In this study we have evaluated in vitro inhibitory potentials of SLN towards PLA(2)s (IC50: 12.5 mu M) and HYs (IC50: 8 mu M) of ECV in addition to docking studies. Further, we have demonstrated the protection of ECV induced local toxicity with 10 mM inhibitor cocktail following 15, 30 min (for hemorrhage and myotoxicity); 60 min (for hemorrhage alone) of ECV injection in murine model. The histological examination of skin and thigh muscle sections taken out from the site of ECV injection substantiated the overall protection offered by inhibitor cocktail. In conclusion, the protective efficacy of inhibitor cocktail is of high interest and can be administered locally alongside ASV to treat severe local toxicity

Not Available

Not AvailableBasic information on genetics and inheritance of quantitative characters, which is necessary to develop future breeding programme, is not widely studied in pigeonpea. Hence, present study was conducted among 5 generations in four pigeonpea crosses to know significance of additive-dominance model, gene action involved in inheritance of quantitative characters, heritability and genetic advance. “Scaling” and “joint scaling test” was significant for most characters indicating that additive-dominance model alone is not enough to explain the inheritance of a character. Though additive variance was more, dominance variance also played important role for most of the traits. Positive and negative alleles were found to be distributed between parents. Additive gene effect (d) was significant for pods per plant and seeds per pod whereas dominance gene effect (h) was more predominant among pod yield and seed yield. Dominance × Dominance inter-allelic interactions (l) was more important than Additive × Additive type (i) for most of the traits studied which could be exploited by selecting individuals based on their performance in recurrent selection. Complementary gene action was observed among many traits with few exhibiting duplicate gene action. Heritability and genetic advance was high indicating the effectiveness of selection. Since dominance effects is also present along with additive effects selection could be practised in later generations to identify high yielding genotypes.Not Availabl

Metabolomics Analysis of Viral Therapeutics

Virotherapy, enabled by recent advances in the transdisciplinary field of biotechnology, has emerged as a powerful tool for use in anticancer treatment, gene therapy, immunotherapy, etc. Examining the effects of viruses and virus-derived immune-modulating therapeutics is of great fundamental and clinical interest. Here we describe a sample preparation protocol for metabolite extraction from virus-infected tissue, in addition to liquid chromatography-mass spectrometry conditions essential for subsequent analysis. This metabolomics approach delivers highly sensitive and specific metabolite information on various biospecimens. Such an approach may be adopted to monitor biological changes in over 30 relevant metabolic pathways in response to viral infection and also viral therapeutics