Transdifferentiation of bovine epithelial cells towards adipocytes in the presence of myoepithelium

Sugathan, Subi,Lee, Sung-Jin,Shiwani, Supriya,Singh, Naresh Kumar Asian Australasian Association of Animal Productio 2020 Animal Bioscience Vol.33 No.2

Objective: Orchastric changes in the mammary glands are vital, especially during lactation. The secretary epithelial cells together with the supporting myoepithelial and stromal cells function cordially to secrete milk. Increase in the number of luminal epithelial cells and a decrease in adipocytes are visible during lactation, whereas the reverse happens in the involution. However, an early involution occurs if the epithelial cells transdifferentiate towards adipocytes during the lactation period. We aimed to inhibit the adipocyte transdifferentiation of luminal cells by restraining the peroxisomal proliferator-activated receptor γ (PPARγ) pathway. Methods: Linolenic acid (LA) and thiazolidinediones (TZDs) induced adipogenesis in mammary epithelial cells were conducted in monolayer, mixed culture as well as in transwell plate co-culture with mammary myoepithelial cells. Results: Co-culture with myoepithelial cells showed higher adipogenic gene expression in epithelial cells under LA+TZDs treatment. Increase in the expressions of PPARγ, CCAAT/enhancer-binding protein α and vimentin in both mRNA as well as protein levels were observed. Whereas, bisphenol A diglycidyl ether treatment blocked LA+TZDs induced adipogenesis, as it could not show a significant rise in adipose related markers. Although comparative results were found in both mixed culture and monolayer conditions, co-culture technic was found to work better than the others. Conclusion: Antagonizing PPARγ pathway in the presence of myoepithelial cells can significantly reduce the adipogenisis in epithelial cells, suggesting therapeutic inhibition of PPARγ can be considered to counter early involution or excessive adipogenesis in mammary epithelium in animals.

Pharmacological Analysis of Vorinostat Analogues as Potential Anti-tumor Agents Targeting Human Histone Deacetylases: an Epigenetic Treatment Stratagem for Cancers

Praseetha, Sugathan,Bandaru, Srinivas,Nayarisseri, Anuraj,Sureshkumar, Sivanpillai Asian Pacific Journal of Cancer Prevention 2016 Asian Pacific journal of cancer prevention Vol.17 No.3

Alteration of the acetylation status of chromatin and other non-histone proteins by HDAC inhibitors has evolved as an excellent epigenetic strategy in treatment of cancers. The present study was sought to identify compounds with positive pharmacological profiles targeting HDAC1. Analogues of Vorinostat synthesized by Cai et al, 2015 formed the test compounds for the present pharmacological evaluation. Hydroxamte analogue 6H showed superior pharmacological profile in comparison to all the compounds in the analogue dataset owing to its better electrostatic interactions and hydrogen bonding patterns. In order to identify compounds with even better high affinity and pharmacological profile than 6H and Vorinostat, virtual screening was performed. A total of 83 compounds similar to Vorinostat and 154 compounds akin to analogue 6H were retrieved. SCHEMBL15675695 (PubCid: 15739209) and AKOS019005527 (PubCid: 80442147) similar to Vorinostat and 6H, were the best docked compounds among the virtually screened compounds. However, in spite of having good affinity, none of the virtually screened compounds had better affinity than that of 6H. In addition SCHEMBL15675695 was predicted to be a carcinogen while AKOS019005527 is Ames toxic. From, our extensive analysis involving binding affinity analysis, ADMET properties predictions and pharmacophoric mappings, we report Vorinostat hydroxamate analogue 6H to be a potential candidate for HDAC inhibition in treatment of cancers through an epigenetic strategy.

Isolation and Characterization of a Feather Degrading Alkalophilic Streptomyces sp. TBG-S13A5 and its Keratinolytic Properties

( Indhuja Selvaraj ),( Sugathan Shiburaj ),( Nediyaparambu Sukumaran Pradeep ),( Vaidyanathan Thankamani ),( Teruvath Koshy Abraham ) 한국미생물생명공학회(구 한국산업미생물학회) 2012 한국미생물·생명공학회지 Vol.40 No.4

Keratinases are of particular interest because of their action on insoluble keratins and generally on a broad range of protein substrates. Alkalophilic and neutrophilic actinomycete strains isolated from different soil samples, rich in keratinaceous substances were screened for keratinolytic activity. An alkalophilic isolate, TBG-S13A5, was found to possess good keratinolytic activity and was able to utilize feather as the sole carbon and nitrogen source. TBG-S13A5 exhibited an off-white aerial mass color with a rectus-flexibilis type of spore chain. The morphological, microscopical and biochemical characters were comparable with that of Streptomyces albidoflavus. Fatty acid methyl ester profiling (FAME) and 16S rDNA sequence analysis confirmed its identity as a strain of S. albidoflavus. Under submerged fermentation conditions, maximum protease production was recorded on the 5th day of incubation at 30℃, using basal broth of pH 9.0 with 0.25% (w/v) white chicken feather. This strain could affect feather degradation when the initial pH was 8 and above and maximum protease production was recorded when the initial pH was around 10.5. The effectiveness of the crude enzyme in destaining and leather dehairing were also demonstrated.

Review on the comparison of effectiveness between denosumab and bisphosphonates in post-menopausal osteoporosis

Biju Benjamin,Mridula Ambwani Benjamin,Myint Swe,Sandheep Sugathan 대한골다공증학회 2016 Osteoporosis and Sarcopenia Vol.2 No.2

Objective: Osteoporosis is a rapidly rising cause of concern for elderly patients. Various classes of drugs are available in the market. Bisphosphonates are considered as a first-line therapy for the prevention and treatment. Denosumab is an antiresorptive agent which is a RANK ligand inhibitor. There is a scarcity of comparison between these two classes of drugs. The aim of this study is to compare efficacy of Bisphosphonates and Denosumab in various parameters. Materials and methods: Literature search was done for randomized controlled trials (RCTs) comparing bisphosphonates with denosumab. RCTs with a treatment period of at least one year with a baseline bone mineral density (BMD) and bone turnover markers (BTM) and follow up values at one year were included in the study. All included studies were also analysed for complications. The study has also been registered in PROSPERO International prospective register of systematic reviews. Results: A total of five RCTs were identified providing data on 3751 participants. In all five studies, the BMD changes at both hip and spine were statistically significant in favour of denosumab. Result was similar in three studies that studied BMD changes at the wrist. Denosumab also produced significant reduction in BTM as early as one month, but at one year there was no difference compared to the bisphosphonates. There was no statistically significant differences in the complication rates. Conclusion: Though both bisphosphonates and denosumab were effective with similar side effects, the latter was statistically superior in increasing the BMD and reducing the BTM. © 2016 The Korean Society of Osteoporosis. Publishing services by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Holstein 젖소에서 조사료 급여 수준이 유방크기, 호르몬 및 산유특성에 미치는 영향: 육성기부터 비유기까지

이병우,수비 수가탄,나레시 쿠마 싱,윤세형,윤병일,Lee, Byung-Woo,Sugathan, Subi,Singh, Naresh Kumar,Yoon, Sei-Hyung,Yoon, Byung-Il 한국초지조사료학회 2013 한국초지조사료학회지 Vol.33 No.4

본 연구결과 조농비가 다른 사료를 각각 급여한 젖소에서 임신초기의 유방 크기는 HF군이 LF군 보다 2.4배 가량 유의하게 컸으나, 임신중기와 착유기 동안에는 두 군 간에 차이가 없었다. Estradiol의 혈중농도는 두 군 모두 사춘기부터 서서히 증가하여 임신기간 동안 사춘기의 2~3.5배가량이 되었으며, 두 군간 유의한 차이는 나타나지 않았다. 착유기 전 기간에 걸쳐서도 estradiol의 농도는 두 군간 차이가 없었다. Progesterone의 혈중 농도는 사춘기부터 증가하기 시작하여 임신중기까지 두 군 모두 비슷한 농도로 유지되었으며, 시험 전 기간에 걸쳐 두 군간 유의한 차이는 없었다. 산유량 4% FCM은 두 군 모두 분만 후 증가하다 LF군은 분만 100일, HF군은 150일을 기점으로 감소하였다. 그러나, 분만 후 50일까지를 제외하고 그 후 전 기간에 걸쳐 양질 조사료 함량이 높은 사료를 급여한 HF군의 젖소에서 산유량이 유의하게 높았으며, 분만 250일 까지도 높은 산유량을 유지하였다. 우유 내 체세포 수는 분만초기를 제외하고 착유기 전 기간 동안 HF군에서 유의하게 감소하였다. 유지율은 분만 후 비유 초기에 LF군에서 다소 높게 나타났으나, 그 이후부터는 두 군간 차이가 없었으며, 그밖에 우유 내 단백율, 고형율, MUN 모두 두 군간 차이는 관찰되지 않았다. 산유량과 체세포 수 및 유지율을 기초로 계산한 유대에 있어 HF군이 LF군에 비하여 최고 141.5% 증대되었다. 본 연구결과로부터 젖소의 양질 조사료의 함량을 적당 수준으로 증가시킴으로써 유방의 크기나 관련 호르몬의 변화 없이 우유의 생산량을 증대시키고 우유의 질을 높일 수 있을 것으로 평가되었다. In the present study, we investigated the effects of high forage diets on the volume of udder, hormone level in blood, and lactation characteristics in the Holstein dairy cow. We divided into two groups; high forage diet [HF, concentrate: forage=4:6 n=41] and low forage diet [LF, 6:4 n=21]. Five cows were selected from each group based on their age for measuring the udder volume and the serum levels of estradiol and progesterone. Lactation characteristics were compared between HF and LF. The udder volume was 2.5 fold larger in HF at early gestation (p<0.01), but no difference was noted afterward. For the hormone levels, no significant difference was found between the groups. In HF, milk yield was significantly increased and maintained high longer, while somatic cell count was approximately 50% lower. Meanwhile, the milk fat content was significantly lower in HF during early lactating phase (p<0.001), but there was no difference thereafter. For milk protein and solid content, and MUN, no differences were found between the groups during lactation. Our results indicated that feeding high forage diets to dairy cows can increase milk yield and quality without notable changes in the udder volume and hormone level.