7 research outputs found

    Go Ark; an ameliorative bio-product (in vitro) on Phenyl induced cytotoxicity

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    Phenyl (PHY) is one of the chemicals which are used as a disinfectant in the world due to its toxic potential. Cleaning workers are directly exposed to it in institutes, hospitals and houses. Cow urine/Go Ark (GA) has been proved as a bioenhancer in many studies. The present study dealt with the in vitro analysis of PHY induced cytotoxicity (CT) on human peripheral blood lymphocytes and ameliorative potential of Distillate cow urine/Go Ark (DGA) and Fresh Go Ark (FGA) as GA is believed to be an elixir in Ayurved. MTT assay was used to study CT and Cell viability % on Human peripheral blood lymphocytes (HPBL) in vitro. CT of PHY was found to be higher than that of DGA and FGA treated groups. This showed that when PHY induced cells were treated with DGA and FGA, they showed increase in the cell viability %. It was also found that FGA had more potential for enhancing cell viability % of HPBL than that of DGA. We suggest that GA can be used as an ameliorative agent on PHY induced CT. It can be explored by in vivo experiments further for its detoxification properties. Now a day, PHY is used in combination with GA for cleaning purposes as “Gonyl”, it may be safe for cleaning workers to use GA based disinfectants to diminish the CT induced due to PHY exposure at the time of cleaning

    Toxicity of Imidacloprid on Peripheral Blood Lymphocytes by MTT Assay and the Ameliorative Effect of Extract of Tinospora cordifolia (Gilloe) Extract

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    Imidacloprid (IMI) is a widely used insecticide which has a specific affinity for insect neonicotinoid acetylcholine receptors. Like all insecticides which are used in excess it tends to bioaccumulate in the environment. So it was thought worthwhile to study its cytotoxicity to human peripheral blood lymphocytes in concentrations ranging from 1.5mM to 4mM after 2 hours and 18 hours exposure by MTT method. Trypan blue test was also used to determine the percentage of living cells. The ameliorative effect of an extract of the stem in water and ethanolic extract of leaves of Tinospora cordifolia (Thunb.) Miers, was also studied. The viability of the lymphocytes showed a fall with increasing concentrations at an exposure of 2 hours. After 18 hours exposure to the IMI only, the viability showed a significant dose dependent drop. Trypan blue test for viability was also conducted. Addition of Tinospora extract raised the viability significantly at 2 hours of incubation. In fact this increase was greatest at 3.5mM and 4mM concentration of drug. The ameliorative effect was maximum at 2 hours. Addition of Tinospora leaf extract showed a significant increase in cell viability at 18 hours of incubation as compared to values obtained with only the drug. Thus a considerable loss of viability of lymphocytes was seen after exposure to the drug in the selected concentrations but herbal extracts seem to help to make the damage less marked. The cells showed a significant rise in viability when incubated with Tinospora leaf extract only, confirming its supportive action in cell proliferation. However, taking into account the evident fall in cell viability caused by exposure to the considerably dilute concentrations tested, caution is needed to prevent over exposure to the pesticide while spraying

    In vitro analysis of the effect of Go Ark on Human Peripheral Blood Lymphocytes

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    Cow is worshiped in India as “Gomata” since ancient time. Its values have been signified in Vedas, Puranas & Ayurveda. Its urine/Go Ark is used in rituals & medicines traditionally in India. The Significance of Cow Urine has been studied by many workers. Now it is available in the market as distillate. Hence this study was designed to assess the potential of Fresh Go Ark (FGA) and Distillate Go Ark (DGA) on Human Peripheral blood lymphocytes (PBL) in Vitro using MTT Assay. It was found that FGA & DGA both had the potential to enhance the cell viability of Human PBL. FGA showed greater potential towards the enhancement of cell viability on Human PBL than that of DGA. However the difference between the impacts of FGA & DGA was not found to be significant when tested through Two way ANOVA

    An in vitro study of cytotoxicity of organophosphate insecticides (Imidacloprid, Profenofos, Dichlorvos) and natural products (Neem oil and Dashparni ark) on human peripheral lymphocytes by MTT and Trypan blue assay

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    It is a well-known fact that the human population of India is increasing very fast. Everybody needs food to survive. Agricultural products must be boosted by adding adequate fertilisers and using appropriate insecticides. Organophosphates are one of the most frequently used insecticides. Their overuse leads to soil contamination by agricultural runoff. The insecticides may enter drinking water as well. Since organophosphates are acetylcholinesterase inhibitors, they can be dangerous for human health if abnormal amounts are present in drinking water or are consumed as residues on fruits and vegetables. Hence, a toxicity study by MTT and Trypan Blue Assay of three common insecticides (Imidacloprid, Profenofos, Dichlorvos) and two natural products (Dashparnik ark and Neem oil) on lymphocytes was taken up. The insecticides were used at concentrations of 1mM, 4mM, 8mM and 12mM. It was found that at 4 hours of incubation at 1mM Imidacloprid showed the greatest drop in viability followed by Dichlorvos and the least harm was caused by Profenofos. The drop was consistent and dose dependent in the case of Profenofos, whereas at a higher concentration the viability generally increased. For 18 hours of incubation, the same trend was observed, but the decrease and increase were more pronounced. In the case of Profenofos and Dichlorvos the viability percent rises above that of the control. It was probably due to the defense mechanism involving the P450 detoxification pathway of the cells, which is activated if they are exposed to a higher concentration of the damaging factors. This is also supported by other workers mentioned in the discussion section of this paper. The damage to the cells, as evident in the fall in viability, was of lesser magnitude when organic insecticides were used. In the case of Neem nano-drop emulsion, a significant fall in viability was noted only at 2mg/ml. However, it is not sprayed as a nano-emulsion because it is not particularly harmful. The fourth insecticide that was taken up for study was Dashparni Ark. In this case, at 5µl/ml of distilled water (obtained by dilution) very little damage was evident, but at higher concentration it boosted the viability. Apparently, the extract of leaves fermented in cow urine and cow dung was less damaging than that of other insecticides. Thus, organic insecticides are safer to use because they are ecofriendly and do not harm non-target organisms. This is written on the basis of MTT assay results

    Whole genome sequencing identifies novel genetic mutations in patients with eczema herpeticum

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    BackgroundEczema herpeticum (EH) is a rare complication of atopic dermatitis (AD) caused by disseminated herpes simplex virus (HSV) infection. The role of rare and/or deleterious genetic variants in disease etiology is largely unknown. This study aimed to identify genes that harbor damaging genetic variants associated with HSV infection in AD with a history of recurrent eczema herpeticum (ADEH+).MethodsWhole genome sequencing (WGS) was performed on 49 recurrent ADEH+ (≥3 EH episodes), 491 AD without a history of eczema herpeticum (ADEH-) and 237 non-atopic control (NA) subjects. Variants were annotated, and a gene-based approach (SKAT-O) was used to identify genes harboring damaging genetic variants associated with ADEH+. Genes identified through WGS were studied for effects on HSV responses and keratinocyte differentiation.ResultsEight genes were identified in the comparison of recurrent ADEH+to ADEH-and NA subjects: SIDT2, CLEC7A, GSTZ1, TPSG1, SP110, RBBP8NL, TRIM15, and FRMD3. Silencing SIDT2 and RBBP8NL in normal human primary keratinocytes (NHPKs) led to significantly increased HSV-1 replication. SIDT2-silenced NHPKs had decreased gene expression of IFNk and IL1b in response to HSV-1 infection. RBBP8NL-silenced NHPKs had decreased gene expression of IFNk, but increased IL1b. Additionally, silencing SIDT2 and RBBP8NL also inhibited gene expression of keratinocyte differentiation markers keratin 10 (KRT10) and loricrin (LOR).ConclusionSIDT2 and RBBP8NL participate in keratinocyte's response to HSV-1 infection. SIDT2 and RBBP8NL also regulate expression of keratinocyte differentiation genes of KRT10 and LOR
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