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    <title>DSpace Collection:</title>
    <link>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/423</link>
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        <rdf:li rdf:resource="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5610" />
        <rdf:li rdf:resource="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5609" />
        <rdf:li rdf:resource="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5497" />
        <rdf:li rdf:resource="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5473" />
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    <dc:date>2026-04-22T12:57:15Z</dc:date>
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  <item rdf:about="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5610">
    <title>Hypoxia-Induced Impairment of Glucose Homeostasis: Sympathovagal Imbalance and the Potential Therapeutic Role of L/N type Calcium Channel Blocker Cilnidipine</title>
    <link>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5610</link>
    <description>Title: Hypoxia-Induced Impairment of Glucose Homeostasis: Sympathovagal Imbalance and the Potential Therapeutic Role of L/N type Calcium Channel Blocker Cilnidipine
Authors: Shrilaxmi Bagali, Pallavi Kanthe, R Chandramouli Reddy, Gouher Banu Shaikh, Sumangala Patil, Kusal Das.</description>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5609">
    <title>Hypoxia-Induced Impairment of Glucose Homeostasis: Sympathovagal Imbalance and the Potential Therapeutic Role of L/N type Calcium Channel Blocker Cilnidipine</title>
    <link>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5609</link>
    <description>Title: Hypoxia-Induced Impairment of Glucose Homeostasis: Sympathovagal Imbalance and the Potential Therapeutic Role of L/N type Calcium Channel Blocker Cilnidipine
Authors: Shrilaxmi Bagali, Pallavi Kanthe, R Chandramouli Reddy, Gouher Banu Shaikh, Sumangala Patil, Kusal Das.</description>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5497">
    <title>The Role of Serum Erythropoietin (EPO) and Vascular Endothelial Growth Factor (VEGF) in Pulse Wave Velocity (PWV) Among Hypertensive Patients: A Cross-Sectional Study</title>
    <link>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5497</link>
    <description>Title: The Role of Serum Erythropoietin (EPO) and Vascular Endothelial Growth Factor (VEGF) in Pulse Wave Velocity (PWV) Among Hypertensive Patients: A Cross-Sectional Study
Authors: Patil, Sumngala
Abstract: Background and objective While hypertension (HTN) is a major health-related threat globally, it is often an under-reported clinical condition as most of the stage I hypertensive patients do not present with any symptoms. The relationship between endogenous oxygen-sensing protein [erythropoietin (EPO) and vascular endothelial growth factor (VEGF)] levels and vascular stress in hypertensive patients is not fully understood as the mechanistic pathway by which these oxygen-sensing proteins alter the vascular physiology and cause hypertension is still a matter of debate. In light of this, we explored the role of these two proteins in the development of vascular stress including increased pulse wave velocity (PWV). We aimed to examine the correlation between oxygen-sensing proteins and vascular stress markers including PWV in hypertensive patients. Materials and methods We conducted a cross-sectional study involving age-matched participants classified into three groups (group 1: normotensive persons, n=36; group 2: stage I hypertensive patients, n=36; and group 3, stage II hypertensive patients, n=36). Adiposity-related parameters such as waist circumference (WC), hip circumference (HC), BMI, and waist-hip ratio (WHR) were measured. BP was recorded manually in resting posture by using a sphygmomanometer. PWV, which predicts the progression of BP and the development of HTN, was recorded using a periscope, which works based on the oscillometric method. Vascular stressinduced oxidative stress parameters [serum malondialdehyde (MDA) and serum nitric oxide (NO)] were also estimated by using a UV spectrophotometer. Quantitative estimations of oxygen-sensing proteins (serum EPO and serum VEGF) were done by using the ELISA kit method. The results were expressed as mean ± standard deviation (SD). The correlation between the variables was done using Spearman’s correlation. A pvalue &lt;0.05 was considered statistically significant. Results Adiposity indices and vascular stiffness parameters were found to be significantly (p &lt;0.05) increased in group 2 and group 3 compared to group 1. The levels of serum MDA were found to be significantly (p&lt;0.05) increased in group 2 and group 3 than group 1, whereas the levels of serum NO were significantly (p&lt;0.05) decreased in group 3 and group 2 than group 1. A significant (p&lt;0.05) positive correlation was observed between the PWV and EPO (r=0.492) while a significant (p&lt;0.05) negative correlation was observed between PWV and VEGF (r=-0.406) among the study population. Conclusion The results are indicative of the influence of vascular stress in stage I and II hypertensive patients. Furthermore, the relationship between oxygen-sensing proteins and vascular stress in hypertensive patients has also been established.</description>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5473">
    <title>Acalabrutinib as a novel hope for the treatment of breast and lung cancer: an in-silico proof of concept</title>
    <link>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/5473</link>
    <description>Title: Acalabrutinib as a novel hope for the treatment of breast and lung cancer: an in-silico proof of concept
Authors: Kulkarni, Prachi
Abstract: Drug repurposing is proved to be a groundbreaking concept in the field of cancer research, accelerating the pace of de novo drug discovery by investigating the anti-cancer activity of the already approved drugs. On the other hand, it got highly benefitted from the advancement in the in-silico tools and techniques, which are used to build up the initial “proof of concept” based on the drug-target interaction. Acalabrutinib (ACL) is a well-known drug for the treatment of hematological malignancies. But, the therapeutic ability of ACL against solid tumors is still unexplored. Thereby, the activity of ACL on breast cancer and lung cancer was evaluated utilizing different computational methods. A series of proteins such as VEGFR1, ALK, BCL2, CXCR-4, mTOR, AKT, PI3K, HER-2, and Estrogen receptors were selected based on their involvement in the progression of the breast as well as lung cancer. A multi-level computational study starting from protein-ligand docking to molecular dynamic (MD) simulations were performed to detect the binding potential of ACL towards the selected proteins. Results of the study led to the identification of ACL as a ligand that showed a high docking score and binding energy with HER-2, mTOR, and VEGFR-1 successively. Whereas, the MD simulations study has also shown good docked complex stability of ACL with HER2 and VEGFR1. Our findings suggest that interaction with those receptors can lead to preventive action on both breast and lung cancer, thus it can be concluded that ACL could be a potential molecule for the same purpose. Communicated by Ramaswamy H. Sarma.</description>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
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