<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OALibJ</journal-id><journal-title-group><journal-title>Open Access Library Journal</journal-title></journal-title-group><issn pub-type="epub">2333-9705</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oalib.1107500</article-id><article-id pub-id-type="publisher-id">OALibJ-111762</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Business&amp;Economics</subject><subject> Chemistry&amp;Materials Science</subject><subject> Computer Science&amp;Communications</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Engineering</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject><subject> Social Sciences&amp;Humanities</subject></subj-group></article-categories><title-group><article-title>
 
 
  Biochemical Effect of Nigella sativa (Black cumin) on Glucose and Lipid Profile among Sudanese Diabetic Patients
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hala</surname><given-names>Altohame Khalaf Allah</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Gad</surname><given-names>Allah Modawe</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abd</surname><given-names>Elkarim A. Abdrabo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Biochemistry Department, Faculty of Medicine and Health Sciences, Omdurman Islamic University, Omdurman, Sudan</addr-line></aff><aff id="aff1"><addr-line>Clinical Chemistry Department, Faculty of Medical Laboratory Sciences-Al-Neelain University, Khartoum, Sudan</addr-line></aff><pub-date pub-type="epub"><day>27</day><month>08</month><year>2021</year></pub-date><volume>08</volume><issue>09</issue><fpage>1</fpage><lpage>8</lpage><history><date date-type="received"><day>7,</day>	<month>May</month>	<year>2021</year></date><date date-type="rev-recd"><day>4,</day>	<month>September</month>	<year>2021</year>	</date><date date-type="accepted"><day>7,</day>	<month>September</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: Diabetes mellitus (DM) is a common chronic disease; it is associated with alterations of blood glucose and lipid profile. Current evidence indicated beneficial effects of some medicinal herbs on metabolic parameters. Aim: The aim of this study was to investigate the effect of Nigella Sativa (NS) supplementation on blood glucose and lipid profile levels among type 2 DM Sudanese patients. Materials and Methods: the experimental study was conducted at Gezira state-Khartoum during the period from November 2019 to February 2020. Forty-five diabetic patients were randomly selected. Study population was classified into three groups; each contained 15 patients; glucose and lipid profile were estimated in all participants three times, the first one in day 0, the second after 15 days of daily intake of NS and the last sample after 30 days. Group 1 was given NS at concentration of 1 gram, and group 2 was given NS at concentration of 2 grams, while group 3 was given at concentration of 3 grams. Results: The included patients in the groups used NS with different dose, showed significant (P &lt; 0.05) improvement with reference to blood glucose, while there was no significant improvement of lipid profile in all groups. Conclusion: Using regular NS can improve blood glucose level but has no effect on serum lipids. Concentration of two grams of NS has a better effect on blood glucose control.
 
</p></abstract><kwd-group><kwd>Diabetes</kwd><kwd> Glucose</kwd><kwd> Herbal Medicine</kwd><kwd> Lipid Profile</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Diabetes mellitus (DM) is a common chronic disease that affects people of all ages and imposes a large economic burden on the health care system. DM is characterized by chronic elevation of blood glucose which is a central factor in the production of reactive oxygen species (ROS) that in turn promote cellular damage and contribute to the development and progression of diabetic complications [<xref ref-type="bibr" rid="scirp.111762-ref1">1</xref>]. Pancreatic β-cells are particularly susceptible to damage by oxidative stress when exposed to chronic hyperglycemia because they are low in free-radical quenching enzymes. Furthermore, ROS can suppress the insulin response and contribute to the development of insulin resistance―a key pathological feature of type 2 DM [<xref ref-type="bibr" rid="scirp.111762-ref1">1</xref>]. Therefore, adequate glycemic control is essential for preventing complications associated with type 2 diabetes. Intensive glucose-lowering strategy has been found to reduce the risk of microvascular endpoints in patients with type 2 diabetes by up to 25% [<xref ref-type="bibr" rid="scirp.111762-ref2">2</xref>]. Moreover, clinical trials showed that a 1% decrease in HbA1c reduces cardiovascular complications by 14% [<xref ref-type="bibr" rid="scirp.111762-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.111762-ref3">3</xref>]. On the other hand, patients with type 2 DM have a complex alteration in plasma lipids characterized by elevated level of triglycerides (TG), decreased level of high-density lipoprotein cholesterol (HDL-c), and a preponderance of the low-density lipoprotein cholesterol (LDL-c). The abnormalities in circulating lipids and lipoproteins are considered to be important risk factors for cardiovascular diseases in diabetic individuals [<xref ref-type="bibr" rid="scirp.111762-ref4">4</xref>]. Nigella sativa (NS) seeds, an annual Ranunculaceae herbaceous plant, have been used in folk medicine to treat mild hypertention [<xref ref-type="bibr" rid="scirp.111762-ref5">5</xref>]. Regarding glucose lowering effects; NS has been reported in different diabetic animal models to be of desired outcome [<xref ref-type="bibr" rid="scirp.111762-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.111762-ref7">7</xref>]. Benhaddou-Andaloussi and colleagues [<xref ref-type="bibr" rid="scirp.111762-ref8">8</xref>] have demonstrated that NS ethanol extract exhibits a remarkable ability in vitro to concomitantly increase insulin secretion, induce proliferation of pancreatic β-cells, and stimulate glucose uptake in skeletal muscle and fat cells. In another study, the same investigators reported that treatment with NS ethanol extract, in diabetic “Merionesshawi” rats, caused a progressive normalization of glycaemia, albeit slower than that of metformin controls and exerted an insulin sensitizing action, compared to diabetic controls [<xref ref-type="bibr" rid="scirp.111762-ref9">9</xref>].</p><p>The protective effect of NS has been attributed to its strong antioxidant properties, which are related to its ability to scavenge various reactive oxygen species [<xref ref-type="bibr" rid="scirp.111762-ref10">10</xref>], block lipid peroxidation as well as enhance antioxidant enzymes [<xref ref-type="bibr" rid="scirp.111762-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.111762-ref12">12</xref>]. In spite of the extensive discussion on the hypoglycemic and antioxidant effects of NS on diabetic animal models; there is still scant evidence about these effects on humans. Najmi and colleagues [<xref ref-type="bibr" rid="scirp.111762-ref13">13</xref>] reported that NS oil (2.5 mL twice daily for 6 weeks) has a beneficial effect on fasting blood glucose, total cholesterol, and LDL-cholesterol in obese diabetics, suggesting that NS oil is effective as an “add-on” therapy in patients of insulin resistance syndrome. The results of a more recent study were carried out, which indicated that NS in a dose of 2 g/day for 12 weeks might be a beneficial adjuvant to oral hypoglycemic agents in type 2 diabetic patients [<xref ref-type="bibr" rid="scirp.111762-ref13">13</xref>]. However, there is still a concern about persistence of these effects upon long-term use of NS. Therefore, the objective of this study was to investigate the effect of NS supplementation on glucose level as well as lipid profile in type 2 Sudanese diabetic patients.</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>The study took place in Gezira State, Central Sudan. Forty-five diabetic patients were randomly selected during the period from November 2019 to February 2020. Study population was classified into three groups containing 15 patients each; glucose as well as lipid paramenters were investigated thrice in all participants in the three groups, one in day 0, other one after 15 days of daily intake of NS and one more 15 days later. Group 1 was given NS at concentration of 1 g, group 2 was given NS at concentration of 2 g while group 3 was given NS at concentration of 3 g. Groups were classified according to glucose level primarily (group one glucose level’s mean was below 180 mg/dL, group two glucose level’s mean was below 220 and more than 180 mg/dL while group three glucose level’s mean was higher than 220 mg/dL). All participants provided written informed consent and they agreed to participate in the study. All participants with cardiovascular problems were excluded.</p><sec id="s2_1"><title>2.1. Sample Collection and Testing</title><p>Under aseptic condition; 5.0 mL of venous blood was taken (after 10 hours fasting) prior and after the intake of NS from each patient by vein puncture technique and were divided into two tubes; one with fluoride oxalate anticoagulant while the other plain (has no anticoagulant), samples were centrifuged at 3000 rpm for five minutes to obtain plasma and serum, respectively. Samples were then pipetted into small eppendorf tubes for measurement of glucose as well as lipid profile. Kits were supplied by Dade Behring, Germany. Assays were performed according to the manufacturer’s instructions, using the automated assay analyzer (Dimension Clinical Chemistry System, Germany). LDL-C was calculated using the Friedewald formula [<xref ref-type="bibr" rid="scirp.111762-ref14">14</xref>].</p></sec><sec id="s2_2"><title>2.2. Statistical Analysis</title><p>All data were extracted to Microsoft office excel (Microsoft office excel for windows 2007) and SPSS (SPSS for windows version 19). Normal distribution of studied variable was examined using T-test. Unpaired T-test and Mann-whiteney U test were also used to assess any significant differences in the means of the studied variables.</p></sec><sec id="s2_3"><title>2.3. Ethical Consideration</title><p>The study approval from the Al-Neelain University Faculty of Medical Laboratory Sciences, all participants were informed of the importance of the study.</p></sec></sec><sec id="s3"><title>3. Results</title><p>The blood glucose was gradually significantly decreased in patients used NS, while cholesterol, triglyceride, LDL and HDL were insignificantly affected in all groups with different dose of NS, as presented in <xref ref-type="table" rid="table1">Table 1</xref>, <xref ref-type="table" rid="table2">Table 2</xref> and <xref ref-type="table" rid="table3">Table 3</xref>. The level of blood glucose was reduced among patients who received one gram of NS to about 32 mg after 30 days of regular use. It is reduced by about 49 mg in the group that used 2 grams. Also, it is reduced by about 39 mg in the group that used 3 grams. This indicated 2 grams of NS has a better effect on the control of blood glucose.</p><p>Regarding lipids, there is an effect among the groups, but there is no clinically significant reduction.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Glucose, cholesterol, HDL, LDL and triglyceride levels among patients treated with one gram of NS</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >P. value</th><th align="center" valign="middle" >30 DAYS N = 15</th><th align="center" valign="middle" >15 DAYS N = 15</th><th align="center" valign="middle" >Before treatment N = 15</th><th align="center" valign="middle" >Variables</th></tr></thead><tr><td align="center" valign="middle" >0.00</td><td align="center" valign="middle" >146 &#177; 44.8</td><td align="center" valign="middle" >166.2 &#177; 51.1</td><td align="center" valign="middle" >178 &#177; 58</td><td align="center" valign="middle" >Glucose</td></tr><tr><td align="center" valign="middle" >0.00</td><td align="center" valign="middle" >219 &#177; 78</td><td align="center" valign="middle" >193 &#177; 39</td><td align="center" valign="middle" >217 &#177; 46</td><td align="center" valign="middle" >Cholesterol</td></tr><tr><td align="center" valign="middle" >0.01</td><td align="center" valign="middle" >58 &#177; 26</td><td align="center" valign="middle" >55.8 &#177; 25.6</td><td align="center" valign="middle" >63 &#177; 28</td><td align="center" valign="middle" >HDL</td></tr><tr><td align="center" valign="middle" >0.10</td><td align="center" valign="middle" >140 &#177; 76</td><td align="center" valign="middle" >110.4 &#177; 75.8</td><td align="center" valign="middle" >127 &#177; 42</td><td align="center" valign="middle" >LDL</td></tr><tr><td align="center" valign="middle" >0.20</td><td align="center" valign="middle" >138 &#177; 62</td><td align="center" valign="middle" >133.7 &#177; 40.3</td><td align="center" valign="middle" >140 &#177; 29</td><td align="center" valign="middle" >Triglycrides</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Glucose, cholesterol, HDL, LDL and triglyceride levels among patients treated with two grams of NS</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >P. value</th><th align="center" valign="middle" >30 DAYS N = 15</th><th align="center" valign="middle" >15 DAYS N = 15</th><th align="center" valign="middle" >Before treatment N = 15</th><th align="center" valign="middle" >Variables</th></tr></thead><tr><td align="center" valign="middle" >0.00</td><td align="center" valign="middle" >139 &#177; 45</td><td align="center" valign="middle" >169 &#177; 71</td><td align="center" valign="middle" >188 &#177; 58</td><td align="center" valign="middle" >Glucose</td></tr><tr><td align="center" valign="middle" >0.00</td><td align="center" valign="middle" >219 &#177; 78</td><td align="center" valign="middle" >196 &#177; 41</td><td align="center" valign="middle" >225 &#177; 25</td><td align="center" valign="middle" >Cholesterol</td></tr><tr><td align="center" valign="middle" >0.01</td><td align="center" valign="middle" >59 &#177; 11</td><td align="center" valign="middle" >57 &#177; 20</td><td align="center" valign="middle" >55 &#177; 02</td><td align="center" valign="middle" >HDL</td></tr><tr><td align="center" valign="middle" >0.14</td><td align="center" valign="middle" >121 &#177; 17</td><td align="center" valign="middle" >115 &#177; 45</td><td align="center" valign="middle" >127 &#177; 44</td><td align="center" valign="middle" >LDL</td></tr><tr><td align="center" valign="middle" >0.24</td><td align="center" valign="middle" >131 &#177; 22</td><td align="center" valign="middle" >123 &#177; 17</td><td align="center" valign="middle" >122 &#177; 35</td><td align="center" valign="middle" >Triglycrides</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Glucose, cholesterol, HDL, LDL and triglyceride levels among patients treated with three grams of NS</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >P. value</th><th align="center" valign="middle" >30 DAYS N = 15</th><th align="center" valign="middle" >15 DAYS N = 15</th><th align="center" valign="middle" >Before treatment N = 15</th><th align="center" valign="middle" >Variables</th></tr></thead><tr><td align="center" valign="middle" >0.00</td><td align="center" valign="middle" >187 &#177; 46</td><td align="center" valign="middle" >202 &#177; 42</td><td align="center" valign="middle" >226 &#177; 44</td><td align="center" valign="middle" >Glucose</td></tr><tr><td align="center" valign="middle" >0.00</td><td align="center" valign="middle" >255 &#177; 82</td><td align="center" valign="middle" >232 &#177; 58</td><td align="center" valign="middle" >258 &#177; 64</td><td align="center" valign="middle" >Cholesterol</td></tr><tr><td align="center" valign="middle" >0.01</td><td align="center" valign="middle" >86 &#177; 51</td><td align="center" valign="middle" >64 &#177; 38</td><td align="center" valign="middle" >76 &#177; 36</td><td align="center" valign="middle" >HDL</td></tr><tr><td align="center" valign="middle" >0.15</td><td align="center" valign="middle" >146 &#177; 53</td><td align="center" valign="middle" >141 &#177; 59</td><td align="center" valign="middle" >133 &#177; 65</td><td align="center" valign="middle" >LDL</td></tr><tr><td align="center" valign="middle" >0.32</td><td align="center" valign="middle" >112 &#177; 54</td><td align="center" valign="middle" >138 &#177; 34</td><td align="center" valign="middle" >146 &#177; 58</td><td align="center" valign="middle" >Triglycerides</td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>The aim of this study was to assess effects of NS on the glucose as well as the lipid parameter’s level. The results of the present study revealed that NS enhanced glycemic control, manifested by the significant reduction in glucose level in all participants compared to the corresponding baseline. This indicates the persistence of NS short term improvement in glycemic control (one month) in type 2 diabetic patients. This was also reported in another study conducted earlier [<xref ref-type="bibr" rid="scirp.111762-ref15">15</xref>]. The reduction in blood glucose level encountered here in agreement with the findings of previous studies conducted on streptozotocin induced diabetic rats treated with crude NS [<xref ref-type="bibr" rid="scirp.111762-ref16">16</xref>], or with NS oil [<xref ref-type="bibr" rid="scirp.111762-ref17">17</xref>]. Moreover, significant decline in blood sugar was recorded when NS volatile oil, 2.5 mL twice daily was added to metformin in the treatment of type 2 diabetic patients or those with insulin resistance syndrome [<xref ref-type="bibr" rid="scirp.111762-ref18">18</xref>]. Regarding lipid profile; findings presented in the current study revealed insignificant reduction in cholesterol, triglycerides and LDL levels. Some findings presented in the current study were in accordance with results present in other studies in the literature while some were not. In a study by Najmi and colleagues, NS in spite of change in LDL and HDL, could not reduce blood cholesterol and triglyceride in metabolic syndrome patients [<xref ref-type="bibr" rid="scirp.111762-ref13">13</xref>]. Ibrahim et al. [<xref ref-type="bibr" rid="scirp.111762-ref19">19</xref>] also did not find any significant change in blood HDL in metabolic syndrome patients with NS supplementation but found reduction of serum cholesterol, LDL, and triglycerides. A study of Husseini and colleagues on type II diabetic patients did not show any significant change in Triglyceride, LDL-, and HDL, with consumption of NS and just showed only reduction of Cholesterol in serum [<xref ref-type="bibr" rid="scirp.111762-ref20">20</xref>]. Dehkordi et al. [<xref ref-type="bibr" rid="scirp.111762-ref21">21</xref>] did not report any change in serum level of Triglyceride and HDL in patients with mild hypertension by NS supplementation. Also, in a study of Qidwai et al., NS supplementation did not have significant effect on lipid profiles [<xref ref-type="bibr" rid="scirp.111762-ref22">22</xref>]. Badar and colleagues recently, in 2017, conducted a study in King Fahd Hospital of the University of Dammam, Saudi Arabia; they indicated a significant decline in choleterol, LDL, cholesterol/HDL and LDL/HDL ratios, moreover, HDL was reported to be significantly elevated as well [<xref ref-type="bibr" rid="scirp.111762-ref23">23</xref>]. However, earlier (in 2016) Mohtashami and colleagues in Chaloos, Northern Iran investigated the effects of bread with NS on Lipid Profile and concluded that no significant association exists regarding triglyceride, cholesterol, LDL and HDL [<xref ref-type="bibr" rid="scirp.111762-ref24">24</xref>]. Earlier (in 2015), Kaatabi and colleagues conducted a study in University of Dammam, Dammam, Saudi Arabia as well titled “Nigella sativa Improves Glycemic Control and Ameliorates Oxidative Stress in Patients with Type 2 Diabetes Mellitus: Placebo Controlled Participant Blinded Clinical Trial”, they concluded a significant relationship between NS intake and the level of glucose [<xref ref-type="bibr" rid="scirp.111762-ref25">25</xref>]. The variations between the previous studies and the current study may be related to the duration time of the study and the dose form of NS. In addition life style and activity factors not included in this study</p><p>From general previous studies conducted addressing this issue, has considerably moderate study populations, further large-scale studies are needed to be conducted for better judge the efficiency of NS in controlling glucose, total cholesterol and LDL levels both in the short as well as the long term.</p></sec><sec id="s5"><title>5. Conclusion</title><p>The results of this study indicated that use of NS was found to be effective in reduction of blood glucose in type 2 DM, regular use of 2 grams has better control effect. But no improvement occurs on serum lipids.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest.</p></sec><sec id="s7"><title>Cite this paper</title><p>Allah, H.A.K., Modawe, G.A. and Abdrabo, A.E.A. (2021) Biochemical Effect of Nigella sativa (Black cumin) on Glucose and Lipid Profile among Sudanese Diabetic Patients. Open Access Library Journal, 8: e7500. https://doi.org/10.4236/oalib.1107500</p></sec></body><back><ref-list><title>References</title><ref id="scirp.111762-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Carvalho, C., Santos, R.X., Cardoso, S., Correia, S., Oliveira, P.J., Santos, M.S., et al. (2009) Doxorubicin: The Good, the Bad and the Ugly Effect. Current Medicinal Chemistry, 16, 3267-3285. https://doi.org/10.2174/092986709788803312</mixed-citation></ref><ref id="scirp.111762-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Mazzone, T. (2010) Intensive Glucose Lowering and Cardiovascular Disease Prevention in Diabetes: Reconciling the Recent Clinical Trial Data. Circulation, 122, 2201-2211. https://doi.org/10.1161/CIRCULATIONAHA.109.913350</mixed-citation></ref><ref id="scirp.111762-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Stratton, I.M., Adler, A.I., Neil, H.A.W., Matthews, D.R., Manley, S.E., Cull, C.A., et al. (2000) Association of Glycaemia with Macrovascular and Microvascular Complications of Type 2 Diabetes (UKPDS 35): Prospective Observational Study. BMJ, 321, 405-412. https://doi.org/10.1136/bmj.321.7258.405</mixed-citation></ref><ref id="scirp.111762-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Andersen, T., Schmidt, J., Thomassen, M., Hornstrup, T., Frandsen, U., Randers, M.B., et al. (2014) A Preliminary Study: Effects of Football Training on Glucose Control, Body Composition, and Performance in Men with Type 2 Diabetes. Scandinavian Journal of Medicine &amp; Science in Sports, 24, 43-56.  
https://doi.org/10.1111/sms.12259</mixed-citation></ref><ref id="scirp.111762-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Tahraoui, A., El-Hilaly, J., Israili, Z. and Lyoussi, B. (2007) Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Hypertension and Diabetes in South-Eastern Morocco (Errachidia Province). Journal of Ethnopharmacology, 110, 105-117. https://doi.org/10.1016/j.jep.2006.09.011</mixed-citation></ref><ref id="scirp.111762-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Alimohammadi, S., et al. (2013) Protective and Antidiabetic Effects of Extract from Nigella sativa on Blood Glucose Concentrations against Streptozotocin (STZ)-Induced Diabetic in Rats: An Experimental Study with Histopathological Evaluation. Diagnostic Pathology, 8, 137. https://doi.org/10.1186/1746-1596-8-137</mixed-citation></ref><ref id="scirp.111762-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Fararh, K., Atoji, Y., Shimizu, Y., Shiina, T., Nikami, H. and Takewaki, T. (2004) Mechanisms of the Hypoglycaemic and Immunopotentiating Effects of Nigella sativa L. Oil in Streptozotocin-Induced Diabetic Hamsters. Research in Veterinary Science, 77, 123-129. https://doi.org/10.1016/j.rvsc.2004.03.002</mixed-citation></ref><ref id="scirp.111762-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Benhaddou-Andaloussi, A., Martineau, L.C., Spoor, D., Vuong, T., Leduc, C., Joly, E., et al. (2008) Antidiabetic Activity of Nigella sativa. Seed Extract in Cultured Pancreatic β-Cells, Skeletal Muscle Cells, and Adipocytes. Pharmaceutical Biology, 46, 96-104. https://doi.org/10.1080/13880200701734810</mixed-citation></ref><ref id="scirp.111762-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Benhaddou-Andaloussi, A., Martineau, L., Vuong, T., Meddah, B., Madiraju, P., Settaf, A., et al. (2011) The in Vivo Antidiabetic Activity of Nigella sativa Is Mediated through Activation of the AMPK Pathway and Increased Muscle Glut4 Content. Evidence-Based Complementary and Alternative Medicine, 2011, Article ID: 538671.  
https://doi.org/10.1155/2011/538671</mixed-citation></ref><ref id="scirp.111762-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Badary, O.A., Taha, R.A., Gamal El-Din, A.M. and Abdel-Wahab, M.H. (2003) Thymoquinone Is a Potent Superoxide Anion Scavenger. Drug and Chemical Toxicology, 26, 87-98. https://doi.org/10.1081/DCT-120020404</mixed-citation></ref><ref id="scirp.111762-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Kanter, M., Coskun, O., Korkmaz, A. and Oter, S. (2004) Effects of Nigella sativa on Oxidative Stress and β-Cell Damage in Streptozotocin-Induced Diabetic Rats. The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology: An Official Publication of the American Association of Anatomists, 279, 685-691. https://doi.org/10.1002/ar.a.20056</mixed-citation></ref><ref id="scirp.111762-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Al Wafai, R.J. (2013) Nigella sativa and Thymoquinone Suppress Cyclooxygenase-2 and Oxidative Stress in Pancreatic Tissue of Streptozotocin-Induced Diabetic Rats. Pancreas, 42, 841-849. https://doi.org/10.1097/MPA.0b013e318279ac1c</mixed-citation></ref><ref id="scirp.111762-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Najmi, A., Nasiruddin, M., Khan, R.A. and Haque, S.F. (2008) Effect of Nigella sativa Oil on Various Clinical and Biochemical Parameters of Insulin Resistance Syndrome. International Journal of Diabetes in Developing Countries, 28, 11.  
https://doi.org/10.4103/0973-3930.41980</mixed-citation></ref><ref id="scirp.111762-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Bamosa, A.O., Kaatabi, H., Lebdaa, F.M., Elq, A. and Al-Sultanb, A. (2010) Effect of Nigella sativa Seeds on the Glycemic Control of Patients with Type 2 Diabetes Mellitus. Indian Journal of Physiology and Pharmacology, 54, 344-354.</mixed-citation></ref><ref id="scirp.111762-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Tremblay, A.J., Morrissette, H., Gagné, J.-M., Bergeron, J., Gagné, C. and Couture, P. (2004) Validation of the Friedewald Formula for the Determination of Low-Density Lipoprotein Cholesterol Compared with β-Quantification in a Large Population. Clinical Biochemistry, 37, 785-790.  
https://doi.org/10.1016/j.clinbiochem.2004.03.008</mixed-citation></ref><ref id="scirp.111762-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Shah, A.S., Khan, G.M., Badshah, A., Shah, S.U., Shah, K.U., Mirza, S.A., et al. (2012) Nigella sativa Provides Protection against Metabolic Syndrome. African Journal of Biotechnology, 11, 10919-10925. https://doi.org/10.5897/AJB-12-890</mixed-citation></ref><ref id="scirp.111762-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Datau, E., Surachmanto, E.E., Pandelaki, K. and Langi, J. (2010) Efficacy of Nigella sativa on Serum Free Testosterone and Metabolic Disturbances in Central Obese Male. Acta Medica Indonesiana, 42, 130-134.</mixed-citation></ref><ref id="scirp.111762-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Meral, I., Yener, Z., Kahraman, T. and Mert, N. (2001) Effect of Nigella sativa on Glucose Concentration, Lipid Peroxidation, Anti-Oxidant Defence System and Liver Damage in Experimentally-Induced Diabetic Rabbits. Journal of Veterinary Medicine Series A, 48, 593-599. https://doi.org/10.1046/j.1439-0442.2001.00393.x</mixed-citation></ref><ref id="scirp.111762-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Ibrahim, R.M., Hamdan, N.S., Ismail, M., Saini, S.M., Abd Rashid, S.N., AbdLatiff, L., et al. (2014) Protective Effects of Nigella sativa on Metabolic Syndrome in Menopausal Women. Advanced Pharmaceutical Bulletin, 4, 29.</mixed-citation></ref><ref id="scirp.111762-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Hosseini, M., Mirkarimi, S., Amini, M., Mohtashami, R., Kianbakht, S. and Fallah, H.H. (2013) Effects of Nigella sativa L. Seed Oil in Type II Diabetic Patients: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial. Journal of Medicinal Plants, 12, 93-99.</mixed-citation></ref><ref id="scirp.111762-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Dehkordi, F.R. and Kamkhah, A.F. (2008) Antihypertensive Effect of Nigella sativa Seed Extract in Patients with Mild Hypertension. Fundamental &amp; Clinical Pharmacology, 22, 447-452. https://doi.org/10.1111/j.1472-8206.2008.00607.x</mixed-citation></ref><ref id="scirp.111762-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Qidwai, W., et al. (2009) Effectiveness, Safety, and Tolerability of Powdered Nigella sativa (kalonji) Seed in Capsules on Serum Lipid Levels, Blood Sugar, Blood Pressure, and Body Weight in Adults: Results of a Randomized, Double-Blind Controlled Trial. The Journal of Alternative and Complementary Medicine, 15, 639-644.  
https://doi.org/10.1089/acm.2008.0367</mixed-citation></ref><ref id="scirp.111762-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Badar, A., et al. (2017) Effect of Nigella sativa Supplementation over a One-Year Period on Lipid Levels, Blood Pressure and Heart Rate in Type-2 Diabetic Patients Receiving Oral Hypoglycemic Agents: Nonrandomized Clinical Trial. Annals of Saudi Medicine, 37, 56-63. https://doi.org/10.5144/0256-4947.2017.56</mixed-citation></ref><ref id="scirp.111762-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Mohtashami, A., et al. (2016) Effects of Bread with Nigella sativa on Lipid Profiles, Apolipoproteins and Inflammatory Factor in Metabolic Syndrome Patients. Clinical Nutrition Research, 5, 89-95. https://doi.org/10.7762/cnr.2016.5.2.89</mixed-citation></ref><ref id="scirp.111762-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Kaatabi, H., et al. (2015) Nigella sativa Improves Glycemic Control and Ameliorates Oxidative Stress in Patients with Type 2 Diabetes Mellitus: Placebo Controlled Participant Blinded Clinical Trial. PLoS ONE, 10, e0113486.  
https://doi.org/10.1371/journal.pone.0113486</mixed-citation></ref></ref-list></back></article>