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  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/8299" />
  <subtitle />
  <id>http://localhost:8080/xmlui/handle/123456789/8299</id>
  <updated>2026-04-08T21:38:36Z</updated>
  <dc:date>2026-04-08T21:38:36Z</dc:date>
  <entry>
    <title>Assessment of Serum Irisin and Vaspin in Women with Polycystic Ovary Syndrome in Mosul City</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9608" />
    <author>
      <name>Khair Alddin Ibrahim, Saba</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9608</id>
    <updated>2025-01-08T03:17:07Z</updated>
    <published>2023-01-01T00:00:00Z</published>
    <summary type="text">Title: Assessment of Serum Irisin and Vaspin in Women with Polycystic Ovary Syndrome in Mosul City
Authors: Khair Alddin Ibrahim, Saba
Abstract: Patients with “polycystic ovary syndrome” (PCOS) may have changes in adipokine levels due to obesity&#xD;
rather than PCOS per se. This should be taken into account as there is a correlation between adipokine&#xD;
levels and BMI. The objective of the subsequent investigation was to measure serum levels of irisin&#xD;
and vaspin in women with PCOS. In the following study, overall, 140 sample size was selected for the&#xD;
evaluation. These 140 were divided into two groups in which 70 women were on the one group which&#xD;
was the intervention group, and 70 women were in control group. The control group of the study were the&#xD;
women who reportedly had regular and normal menstrual cycle. The results indicated high values of vaspin&#xD;
and irisin. The results of this study and previously published literature suggest that both adipocytokines&#xD;
are associated with high blood glucose levels and higher BMI, and finally, both values remain higher in&#xD;
women with PCOS. Vaspin and irisin could be considered as a biomarker for prognosis and therapy followup&#xD;
in patients with PCOS.&#xD;
Key words: Vaspin, Irisin, Insulin, Testosterone, LH, FSH, PCOS.</summary>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Lisinopril-Induced CD34 Bone Healing Marker</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9607" />
    <author>
      <name>M. Alsaffar, Omar</name>
    </author>
    <author>
      <name>T. Al-Saffar, Maha</name>
    </author>
    <author>
      <name>S. Mahmood, Abdulsattar</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9607</id>
    <updated>2025-01-08T03:15:51Z</updated>
    <published>2023-01-01T00:00:00Z</published>
    <summary type="text">Title: Lisinopril-Induced CD34 Bone Healing Marker
Authors: M. Alsaffar, Omar; T. Al-Saffar, Maha; S. Mahmood, Abdulsattar
Abstract: Background: Lisinopril is an angiotensin-converting enzyme (ACE) inhibitor that is commonly used to treat&#xD;
high blood pressure and heart failure. While it is generally well-tolerated, some studies have suggested&#xD;
that it may affect bone healing, suggesting that lisinopril treatment was associated with an increase in&#xD;
the CD34 bone healing marker in patients with tibial fractures. CD34 is a protein that is involved in the&#xD;
formation of new blood vessels and has been shown to play a role in bone healing. Methods: The study&#xD;
used 24 rabbits with artificially induced tibial bone fracture divided into 4 groups (6 rabbits each), the&#xD;
control group treated with distilled water and 3 groups treated with lisinopril. Each group were sacrificed&#xD;
for immunohistochemical study on 3 timepoints at day 7, 14, and 21. Results: Indicated that the lisinopril&#xD;
group had significantly higher levels of CD34 than the control group. Conclusion: While the results of&#xD;
this study suggest that lisinopril may have a positive effect on bone healing, more research is needed to&#xD;
confirm these findings and to determine the mechanisms by which lisinopril may affect bone healing. It&#xD;
is also important to note that lisinopril may have other potential side effects, and patients should discuss&#xD;
any concerns with their healthcare provider.&#xD;
Key words: Lisinopril, Bone healing, Inflammation, Bone injury, CD34</summary>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Computational and Pharmacokinetic Investigation of Some Heterocyclic Amide Derivatives as Cyclooxygenase Inhibitors: An In-Silico Approach</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9606" />
    <author>
      <name>Kabir, Emranul</name>
    </author>
    <author>
      <name>Khan Noyon, M. R. O.</name>
    </author>
    <author>
      <name>Uzzaman, Monir</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9606</id>
    <updated>2025-01-08T03:12:36Z</updated>
    <published>2023-01-01T00:00:00Z</published>
    <summary type="text">Title: Computational and Pharmacokinetic Investigation of Some Heterocyclic Amide Derivatives as Cyclooxygenase Inhibitors: An In-Silico Approach
Authors: Kabir, Emranul; Khan Noyon, M. R. O.; Uzzaman, Monir
Abstract: The two most significant as well as historically important non-steroidal and anti-inflammatory medications&#xD;
(NSAIDs), aspirin and ibuprofen, are frequently used to treat fever, pain, and inflammation. By blocking the&#xD;
activity of cyclooxygenase (COX), it can prevent the production of prostaglandin. In an effort to examine the&#xD;
physiochemical and biological properties of some heterocyclic amide derivatives and quantum mechanical&#xD;
computations have been used to analyze the compounds. To clarify the thermochemical, molecular orbital,&#xD;
and equilibrium geometrical features in the gas phase, density functional theory (DFT) with the B3LYP/6-&#xD;
31G basis set has been used. Binding affinities and modes of heterocyclic amide analogs have been&#xD;
investigated on human cyclooxygenase (COX-1 and COX-2) proteins (6Y3C and 5F19) using molecular&#xD;
docking as well as nonbonding interactions. Results from geometry and thermochemical analysis support&#xD;
the chemical sustainability of all the structures. Most of the compounds exhibited a significant affinity&#xD;
for binding to the receptor protein (5F19) than the standard drugs aspirin and ibuprofen. The improved&#xD;
pharmacokinetic features of certain derivatives with reduced acute oral toxicity were revealed by ADMET&#xD;
prediction. Overall, four heterocyclic amide analogs 3-6 were found to be more efficient in inhibiting COX-&#xD;
2 (5F19) than COX-1 (6Y3C), suggesting that they may be useful as COX-2-related inflammation drug&#xD;
candidates.&#xD;
Key words: Cyclooxygenase (COX), Heterocyclic amide derivatives, Molecular Docking, ADMET.</summary>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Inflammatory Thyroid Changes Following Serotonin Receptor Blocking in Experimental Rats</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9605" />
    <author>
      <name>N Dawood, Muthear</name>
    </author>
    <author>
      <name>A. Aldabbagh, Karam</name>
    </author>
    <author>
      <name>Alsarraf, Zahraa</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9605</id>
    <updated>2025-01-08T03:12:41Z</updated>
    <published>2023-01-01T00:00:00Z</published>
    <summary type="text">Title: Inflammatory Thyroid Changes Following Serotonin Receptor Blocking in Experimental Rats
Authors: N Dawood, Muthear; A. Aldabbagh, Karam; Alsarraf, Zahraa
Abstract: According to studies, a pathophysiological feature of schizophrenia may be a dysregulation of the&#xD;
inflammatory immune response. Conversely, antipsychotic medications have been found to have&#xD;
an immunosuppressive effect in patients with schizophrenia; however, this has not been consistently&#xD;
observed in different studies. The purpose of the following study is to compare the effects of risperidone&#xD;
with aripiprazole on thyroid function as it relates to inflammatory markers (CRP). This study was based&#xD;
on a randomized controlled trial. A total of thirty rats were recruited for the experiment and were kept in&#xD;
the artificial, and optimal environment. The rats were divided into three groups; each group has an equal&#xD;
number of rats which was 10 rats each. The first group was the control group which received the placebo,&#xD;
in the second group, there were 10 rats too, which was known as the risperidone group. Each rat received&#xD;
20mg/kg/day through I/V. The third group is known as the aripiprazole group which received the drug from&#xD;
the intravenous route, 10mg/kg//day. In the results, the summarized values represented that all the mean&#xD;
values before and after the treatment remained less than 3.0. From the results and other evidence, it can&#xD;
be said that although the subjects who receive the following results do not require regular or frequent&#xD;
monitoring of thyroid hormones in long-term use and in the use of the drug in higher concentration there&#xD;
must be a check as long term use is associated with hyperthyroidism.&#xD;
Key words: Thyroid, FT3, FT4, Thyroxine, Tri-iodothyronine, Aripiprazole, Risperidone.</summary>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </entry>
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