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Dive into the research topics where Nitin A. Das is active.

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Featured researches published by Nitin A. Das.


American Journal of Transplantation | 2007

A Mouse Model of Orthotopic Vascularized Aerated Lung Transplantation

M. Okazaki; Alexander S. Krupnick; C.G. Kornfeld; J. Lai; Jon H. Ritter; Steven B. Richardson; H.J. Huang; Nitin A. Das; G. A. Patterson; Andrew E. Gelman; Daniel Kreisel

Outcomes after lung transplantation are markedly inferior to those after other solid organ transplants. A better understanding of cellular and molecular mechanisms contributing to lung graft injury will be critical to improve outcomes. Advances in this field have been hampered by the lack of a mouse model of lung transplantation. Here, we report a mouse model of vascularized aerated single lung transplantation utilizing cuff techniques. We show that syngeneic grafts have normal histological appearance with minimal infiltration of T lymphocytes. Allogeneic grafts show acute cellular rejection with infiltration of T lymphocytes and recipient‐type antigen presenting cells. Our data show that we have developed a physiological model of lung transplantation in the mouse, which provides ample opportunity for the study of nonimmune and immune mechanisms that contribute to lung allograft injury.


Academic Radiology | 2010

Effects of CT section thickness and reconstruction kernel on emphysema quantification relationship to the magnitude of the CT emphysema index.

David S. Gierada; Andrew J. Bierhals; Cliff K. Choong; Seth T. Bartel; Jon H. Ritter; Nitin A. Das; Cheng Hong; Thomas K. Pilgram; Kyongtae T. Bae; Bruce R. Whiting; Jason C. Woods; James C. Hogg; Barbara A. Lutey; Richard J. Battafarano; Joel D. Cooper; Bryan F. Meyers; G. Alexander Patterson

RATIONALE AND OBJECTIVES Computed tomography (CT) section thickness and reconstruction kernel each influence CT measurements of emphysema. This study was performed to assess whether their effects are related to the magnitude of the measurement. MATERIALS AND METHODS Low-radiation-dose multidetector CT was performed in 21 subjects representing a wide range of emphysema severity. Images were reconstructed using 20 different combinations of section thickness and reconstruction kernel. Emphysema index values were determined as the percentage of lung pixels having attenuation lower than multiple thresholds ranging from -960 HU to -890 HU. The index values obtained from the different thickness-kernel combinations were compared by repeated measures analysis of variance and Bland-Altman plots of mean versus difference in all subjects, and correlated with quantitative histology (mean linear intercept, Lm) in a subset of resected lung specimens. RESULTS The effects of section thickness and reconstruction kernel on the emphysema index were significant (P < .001) and diminished as the index attenuation threshold was raised. The changes in index values from changing the thickness-kernel combination were largest for subjects with intermediate index values (10%-30%), and became progressively smaller for those with lower and higher index values. This pattern was consistent regardless of the thickness-kernel combinations compared and the HU threshold used. Correlations between the emphysema index values obtained with each thickness-kernel combination and Lm ranged from r = 0.55-0.68 (P = .007-.03). CONCLUSION The effects of CT section thickness and kernel on emphysema index values varied systematically with the magnitude of the emphysema index. All reconstruction techniques provided significant correlations with quantitative histology.


Academic Radiology | 2010

Original investigationEffects of CT Section Thickness and Reconstruction Kernel on Emphysema Quantification: Relationship to the Magnitude of the CT Emphysema Index

David S. Gierada; Andrew J. Bierhals; Cliff K. Choong; Seth T. Bartel; Jon H. Ritter; Nitin A. Das; Cheng Hong; Thomas K. Pilgram; Kyongtae T. Bae; Bruce R. Whiting; Jason C. Woods; James C. Hogg; Barbara A. Lutey; Richard J. Battafarano; Joel D. Cooper; Bryan F. Meyers; G. Alexander Patterson

RATIONALE AND OBJECTIVES Computed tomography (CT) section thickness and reconstruction kernel each influence CT measurements of emphysema. This study was performed to assess whether their effects are related to the magnitude of the measurement. MATERIALS AND METHODS Low-radiation-dose multidetector CT was performed in 21 subjects representing a wide range of emphysema severity. Images were reconstructed using 20 different combinations of section thickness and reconstruction kernel. Emphysema index values were determined as the percentage of lung pixels having attenuation lower than multiple thresholds ranging from -960 HU to -890 HU. The index values obtained from the different thickness-kernel combinations were compared by repeated measures analysis of variance and Bland-Altman plots of mean versus difference in all subjects, and correlated with quantitative histology (mean linear intercept, Lm) in a subset of resected lung specimens. RESULTS The effects of section thickness and reconstruction kernel on the emphysema index were significant (P < .001) and diminished as the index attenuation threshold was raised. The changes in index values from changing the thickness-kernel combination were largest for subjects with intermediate index values (10%-30%), and became progressively smaller for those with lower and higher index values. This pattern was consistent regardless of the thickness-kernel combinations compared and the HU threshold used. Correlations between the emphysema index values obtained with each thickness-kernel combination and Lm ranged from r = 0.55-0.68 (P = .007-.03). CONCLUSION The effects of CT section thickness and kernel on emphysema index values varied systematically with the magnitude of the emphysema index. All reconstruction techniques provided significant correlations with quantitative histology.


Journal of Endourology | 2009

Selective versus nonselective arterial clamping during laparoscopic partial nephrectomy: impact upon renal function in the setting of a solitary kidney in a porcine model.

Brian M. Benway; Geneva Baca; Sam B. Bhayani; Nitin A. Das; Matthew D. Katz; Dilmer L. Diaz; Keegan L. Maxwell; Khalid H. Badwan; Michael Talcott; Helen Liapis; Jose M. Cabello; Ramakrishna Venkatesh; Robert S. Figenshau

INTRODUCTION Laparoscopic partial nephrectomy has emerged as a standard of care for small renal masses. Nevertheless, there remains concern over the potential for irreversible insult to the kidney as a result of exposure to warm ischemia. We aim to investigate the utility of selective segmental arterial clamping as a means to reduce the potential for ischemic damage to a solitary kidney during laparoscopic partial nephrectomy utilizing a porcine model. MATERIALS AND METHODS A total of 20 domestic swine were randomized into four equal groups. Each subject underwent laparoscopic radical nephrectomy to create the condition of a solitary kidney. On the contralateral side, a laparoscopic lower pole partial nephrectomy was performed, employing either selective or nonselective vascular clamping for either 60 or 90 minutes. Postoperatively, clinical status and serial serum studies were closely monitored for 1 week. RESULTS There were no intraoperative complications. The 90-minute nonselective clamping produced devastating effects, resulting in rapid deterioration into florid renal failure within 72 hours. The 60-minute nonselective clamping group experienced modest but significant rises in both blood urea nitrogen and creatinine. Both 60- and 90-minute selective clamping groups performed well, with no significant rises in creatinine over a 7-day period, and no instances of renal failure. CONCLUSIONS Selective arterial clamping is a safe and feasible means of vascular control during laparoscopic partial nephrectomy. In the porcine model, selective clamping appears to improve functional outcomes during prolonged periods of warm ischemic insult. Prospective evaluation of the technique in humans is necessary to determine if selective arterial control confers long-term functional benefits in patients with limited renal reserve.


BMC Surgery | 2008

Robotic assisted Laparoscopic partial Nephrectomy for suspected Renal Cell Carcinoma: Retrospective review of surgical outcomes of 35 Cases

Sam B. Bhayani; Nitin A. Das

BackgroundA standard of care for the treatment of small renal masses is partial nephrectomy. The open and laparoscopic approaches have been well described in the literature. Robotic assistance may augment partial nephrectomy by aiding in dissection and renal reconstruction. In this communication we describe the surgical outcomes of 35 patients undergoing robotic partial nephrectomy.MethodsPatient records and databases were reviewed for 35 consecutive patients undergoing RPN. Clinical, pathological, and radiographic data were obtained. The data was deidentified.ResultsThirty five patients successfully underwent RPN. An additional 2 patients were converted to other nephron sparing procedures. Mean tumor size was 2.8 cm, and mean OR time was 142 minutes. Mean warm ischemia time was 20 minutes. All margins were negative. There were 4 complications, and no patients required reoperation.ConclusionRobotic partial nephrectomy can produce excellent initial results. Further studies should be performed to compare the outcomes to laparoscopic and open operations.


Journal of Magnetic Resonance Imaging | 2009

Effects of diffusion time on short‐range hyperpolarized 3He diffusivity measurements in emphysema

David S. Gierada; Jason C. Woods; Andrew J. Bierhals; Seth T. Bartel; Jon H. Ritter; Cliff K. Choong; Nitin A. Das; Cheng Hong; Thomas K. Pilgram; Yulin V. Chang; Richard E. Jacob; James C. Hogg; Richard J. Battafarano; Joel D. Cooper; Bryan F. Meyers; G. Alexander Patterson; Dmitriy A. Yablonskiy; Mark S. Conradi

To characterize the effect of diffusion time on short‐range hyperpolarized 3He magnetic resonance imaging (MRI) diffusion measurements across a wide range of emphysema severity.


Cellular Signalling | 2013

CIKS (Act1 or TRAF3IP2) mediates high glucose-induced endothelial dysfunction.

Balachandar Venkatesan; Anthony J. Valente; Nitin A. Das; Andrea J. Carpenter; Tadashi Yoshida; Jean Luc Delafontaine; Ulrich Siebenlist; Bysani Chandrasekar

Hyperglycemia-induced endothelial dysfunction is characterized by enhanced inflammatory cytokine and adhesion molecule expression, and endothelial-monocyte adhesion. The adapter molecule CIKS (connection to IKK and SAPK/JNK; also known as Act1 or TRAF3IP2) is an upstream regulator of NF-κB and AP-1, and plays a role in inflammation and injury. Here we show that high glucose (HG; 25mM vs. 5mM d-glucose)-induced endothelial-monocyte adhesion and inhibition of endothelial cell (EC) migration were both reversed by CIKS knockdown. In EC, HG induced CIKS mRNA and protein expression via DPI-inhibitable Nox4-dependent ROS generation. Further, HG induced CIKS transcription and enhanced CIKS promoter-dependent reporter gene activation via Nox4, ROS, AP-1 and C/EBP. Coimmunoprecipitation and immunoblotting revealed CIKS/IKKβ/JNK physical association under basal conditions that was enhanced by HG treatment. Importantly, CIKS knockdown inhibited HG-induced (i) IKKβ and JNK phosphorylation, (ii) p65 and c-Jun nuclear translocation, and (iii) NF-κB- and AP-1-dependent proinflammatory cytokine, chemokine, and adhesion molecule expression. Similar to HG, the deleterious metabolic products of chronic hyperglycemia, AGE-HSA, AOPPs-HSA and oxLDL, also induced CIKS-dependent endothelial dysfunction. Notably, aortas from streptozotocin-induced and the autoimmune type 1 diabetic NOD and Akita mice showed enhanced DPI-inhibitable ROS generation and CIKS expression. Since CIKS mediates high glucose-induced NF-κB and AP-1-dependent inflammatory signaling and endothelial dysfunction, targeting CIKS may delay progression of vascular diseases during diabetes mellitus and atherosclerosis.


Journal of Molecular and Cellular Cardiology | 2016

Metformin inhibits aldosterone-induced cardiac fibroblast activation, migration and proliferation in vitro, and reverses aldosterone + salt-induced cardiac fibrosis in vivo

Srinivas Mummidi; Nitin A. Das; Andrea J. Carpenter; Hemanthkumar Kandikattu; Maike Krenz; Ulrich Siebenlist; Anthony J. Valente; Bysani Chandrasekar

The overall goals of this study were to investigate whether metformin exerts anti-fibrotic effects in aldosterone (Aldo)+salt-treated wild type mouse hearts, and determine the underlying molecular mechanisms in isolated adult cardiac fibroblasts (CF). In vitro, Aldo induced CF activation, migration, and proliferation, and these effects were inhibited by metformin. Further, Aldo induced PPM1A (Protein Phosphatase Magnesium Dependent 1A) activation and inhibited AMPK phosphorylation. At a pharmacologically relevant concentration, metformin restored AMPK activation, and inhibited Aldo-induced Nox4/H2O2-dependent TRAF3IP2 induction, pro-inflammatory cytokine expression, and CF migration and proliferation. Further, metformin potentiated the inhibitory effects of spironolactone, a mineralocorticoid receptor antagonist, on Aldo-induced collagen expression, and CF migration and proliferation. These results were recapitulated in vivo, where metformin reversed Aldo+salt-induced oxidative stress, suppression of AMPK activation, TRAF3IP2 induction, pro-inflammatory cytokine expression, and cardiac fibrosis, without significantly modulating systolic blood pressure. These in vitro and in vivo data indicate that metformin has the potential to reduce adverse cardiac remodeling in hypertensive heart disease.


The Journal of Thoracic and Cardiovascular Surgery | 2009

Apyrase treatment prevents ischemia-reperfusion injury in rat lung isografts

Seiichiro Sugimoto; Xue Lin; J. Lai; M. Okazaki; Nitin A. Das; Wenjun Li; Alexander S. Krupnick; Ridong Chen; Soon Seog Jeong; G.A. Patterson; Daniel Kreisel; Andrew E. Gelman

OBJECTIVE Endothelial cells express the ectoenzyme ectonucleoside adenosine triphosphate diphosphohydrolase, an apyrase that inhibits vascular inflammation by catalyzing the hydrolysis of adenosine triphosphate and adenosine diphosphate. However, ectonucleoside adenosine triphosphate diphosphohydrolase expression is rapidly lost following oxidative stress, leading to the potential for adenosine triphosphate and related purigenic nucleotides to exacerbate acute solid organ inflammation and injury. We asked if administration of a soluble recombinant apyrase APT102 attenuates lung graft injury in a cold ischemia reperfusion model of rat syngeneic orthotopic lung transplantation. METHODS Male Fisher 344 donor lungs were cold preserved in a low-potassium dextrose solution in the presence or absence of APT102 for 18 hours prior to transplantation into syngeneic male Fisher 344 recipients. Seven minutes after reperfusion, lung transplant recipients received either a bolus of APT102 or vehicle (saline solution). Four hours after reperfusion, APT102- and saline solution-treated groups were evaluated for lung graft function and inflammation. RESULTS APT102 significantly reduced lung graft extracellular pools of adenosine triphosphate and adenosine diphosphate, improved oxygenation, and protected against pulmonary edema. Apyrase treatment was associated with attenuated neutrophil graft sequestration and less evidence of tissue inflammation as assessed by myeloperoxidase activity, expression of proinflammatory mediators, and numbers of apoptotic endothelial cells. CONCLUSIONS Administration of a soluble recombinant apyrase promotes lung function and limits the tissue damage induced by prolonged cold storage, indicating that extracellular purigenic nucleotides play a key role in promoting ischemia-reperfusion injury following lung transplantation.


Journal of Computer Assisted Tomography | 2010

Emphysema quantification in inflation-fixed lungs using low-dose computed tomography and 3He magnetic resonance imaging.

David S. Gierada; Jason C. Woods; Richard E. Jacob; Andrew J. Bierhals; Cliff K. Choong; Seth T. Bartel; Yulin V. Chang; Nitin A. Das; Cheng Hong; Barbara A. Lutey; Jon H. Ritter; Thomas K. Pilgram; Joel D. Cooper; G. Alexander Patterson; Richard J. Battafarano; Bryan F. Meyers; Dmitriy A. Yablonskiy; Mark S. Conradi

Objective: To evaluate the use of inflation-fixed lung tissue for emphysema quantification with computed tomography (CT) and 3He magnetic resonance (MR) diffusion imaging. Methods: Fourteen subjects representing a range of chronic obstructive pulmonary disease severity who underwent complete or lobar lung resection were studied. Computed tomographic measurements of lung attenuation and MR measurements of the hyperpolarized 3He apparent diffusion coefficient (ADC) in resected specimens fixed in inflation with heated formalin vapor were compared with measurements obtained before fixation. Results: The mean (SD) CT emphysema indices were 56% (17%) before and 58% (19%) after fixation (P = 0.77; R = 0.76). Index differences correlated with differences in lung volume (R2 = 0.47). The mean (SD) 3He ADCs were 0.40 (0.15) cm2/s before and 0.39 (0.14) cm2/s after fixation (P = 0.03, R = 0.98). The CT emphysema index and the 3He ADC were correlated before (R = 0.89) and after fixation (R = 0.79). Conclusions: Concordance of CT and 3He MR imaging measurements in unfixed and inflation-fixed lungs supports the use of inflation-fixed lungs for quantitative imaging studies in emphysema.

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Daniel Kreisel

Washington University in St. Louis

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Andrew E. Gelman

Washington University in St. Louis

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J. Lai

Washington University in St. Louis

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Scott B. Johnson

University of Texas Health Science Center at San Antonio

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Andrea J. Carpenter

University of Texas Health Science Center at San Antonio

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Daniel T. DeArmond

University of Texas Health Science Center at San Antonio

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G. Alexander Patterson

Washington University in St. Louis

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