<?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">ABB</journal-id><journal-title-group><journal-title>Advances in Bioscience and Biotechnology</journal-title></journal-title-group><issn pub-type="epub">2156-8456</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/abb.2016.712048</article-id><article-id pub-id-type="publisher-id">ABB-72581</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></subj-group></article-categories><title-group><article-title>
 
 
  Chemical Composition and Antioxidant Potential of &lt;i&gt;Pistacia lentiscus&lt;/i&gt; L. Essential Oil from Oran (Algeria)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hamiani</surname><given-names>Abdelkader</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kambouche</surname><given-names>Nadia</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bellahouel</surname><given-names>Salima</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Organic Synthesis Laboratory, Chemistry Department, Faculty of Exact Sciences and Applied, Oran 1 Ahmed Benbella University, Oran, Algeria</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>hamianiaek@gmail.com(HA)</email>;<email>kambouche@yahoo.fr(KN)</email>;<email>salimabellahouel@yahoo.fr(BS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>07</day><month>12</month><year>2016</year></pub-date><volume>07</volume><issue>12</issue><fpage>539</fpage><lpage>544</lpage><history><date date-type="received"><day>October</day>	<month>29,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>December</month>	<year>4,</year>	</date><date date-type="accepted"><day>December</day>	<month>7,</month>	<year>2016</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>
 
 
  Essential oil from the leaves of 
  Pistacia lentiscus L. growing in the Oran region in the west of Algeria was obtained by hydrodistillation with a 1.26 % yield on a dry weight basis. Spectrophotometric analyses were employed to highlight the scavenger capacity of this oil using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) test. Twenty compounds were identified by GC and CG/MS analyses, and the main part of the compounds of the oil was terpinene-4-ol (41.24%) and 
  α-terpineol (7.31%), 
  α-pinene (9.48%), limonene (09.11%), 
  β-myrcene (10.5%), 
  p-cymene (8.67%) and 
  α-phellandrene (2.20%), 
  β-caryophyllene (12.62%) as major compounds. The DPPH test shows that 
  Pistacia lentiscus essential oil possesses antiradical activity. A linear correlation (correlation coefficient 
  R
  <sup>2</sup> = 0.995, P &lt; 0.001) was found between the reduction of DPPH stable free radical and the concentration of 
  Pistacia lentiscus essential oil.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Pistacia lentiscus&lt;/i&gt;</kwd><kwd> Terpinene-4-ol</kwd><kwd> Essential Oil</kwd><kwd> Antioxidant Activity</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Pistacia lentiscus L. is an aromatic member of the Anacardiaceae family. In Algeria, P. lentiscus L. occurs in various regions, the aerial parts of P. lentiscus L. has traditionally been used against several diseases [<xref ref-type="bibr" rid="scirp.72581-ref1">1</xref>] . Mastic gum from Pistacia has been used by folkloric medicine for the relief of upper abdominal discomfort, stomachaches, dyspepsia and peptic ulcer [<xref ref-type="bibr" rid="scirp.72581-ref2">2</xref>] .</p><p>Several biological activities have been attributed to the essential oil from aerial parts of P. lentiscus L. such as their antifungal, antibacterial an antimicrobial effect [<xref ref-type="bibr" rid="scirp.72581-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.72581-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.72581-ref5">5</xref>] .</p><p>Some works reported the chemical composition of the essential oil from aerial parts of P. lentiscus L. of diverse countries of the Mediterranean region [<xref ref-type="bibr" rid="scirp.72581-ref6">6</xref>] - [<xref ref-type="bibr" rid="scirp.72581-ref20">20</xref>] . The chemi- cal composition of the essential oil derived from the aerial parts is not clear; it is greatly influenced by both geographical origin and isolation technique.</p><p>The aim of this work was to evaluate antioxidant activities of the essential oil from aerial parts of P. lentiscus L from the region of Oran (Algeria), in relation with the composition of their compounds.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Plant Material</title><p>Leaves of Pistacia lentiscus of the region of Oran were collected in June 2015, during the period of full flowering. Voucher specimens were identified and deposited in the herbarium of the Agricultural Institute in Algeries, Algeria.</p></sec><sec id="s2_2"><title>2.2. Isolation of the Essential Oil</title><p>The air-dried plant material (80 g), both leaves and flowers, was hydrodistilled in an all- glass apparatus according to the method recommended by the European Pharmacopoeia [<xref ref-type="bibr" rid="scirp.72581-ref21">21</xref>] . The essential oil obtained was dried over anhydrous sodium sulfate. Yield based on dry weight of the sample was 1.26%.</p></sec><sec id="s2_3"><title>2.3. GC</title><p>Analytical GC was carried out on a Varian (Palo Alto, CA) model 3300 gas chromato- graph fitted with a fused silica MFE1 capillary column (50 m &#215; 0.25 mm, film thickness 0.25 &#181;m), with N<sub>2</sub> as the carrier gas at a flow rate of 1.5 mL/minute, in split mode, with the temperature programmed to rise from 95˚C to 240˚C at 4˚C/minute. The injector temperature was 250˚C, the detector used was a flame ionization detector, and the detector temperature was 300˚C. Injection volume for all samples was 0.1 &#181;l.</p></sec><sec id="s2_4"><title>2.4. GC/MS</title><p>Analyses were carried out on an Agilent (Palo Alto) 6890 gas chromatograph fitted with a fused Agilent 19091S-433 HP-5MS column (30.0 m &#215; 0.25 mm; film thickness 0.30 &#181;m; temperature programmed from 40˚C to 280˚C at 4˚C/minute) with He as the carrier gas at a flow rate of 1 ml/minute. The chromatograph was coupled to an HP 5973 A mass spectrometer (Hewlett Packard, Palo Alto).</p></sec><sec id="s2_5"><title>2.5. Identification of Components</title><p>Most constituents were identified by means of GC/MS. Some components were tentatively identified by comparing their retention indices on both chromatographic columns with those of authentic compounds and with literature data [<xref ref-type="bibr" rid="scirp.72581-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.72581-ref23">23</xref>] .</p></sec><sec id="s2_6"><title>2.6. Antioxidant Test Free Radical Scavenging Activity (DPPH) Method</title><p>The antioxidant activity was measured by a modification of the DPPH radical scavenging method of Ramos et al. [<xref ref-type="bibr" rid="scirp.72581-ref24">24</xref>] Two hundred microliters of distilled water was mixed with 160 &#181;L of DPPH (0.5 mM in ethanol), and then 40-L samples of the oil in ethanol (ranging from 2.50 to 20 &#181;L/mL) were added. The mixture was shaken and left to stand at room temperature. The absorbance (A) was measured 30 minutes later at 517 nm.</p><p>The inhibition potential (IP) (as a percentage) is measured using the formula:</p><disp-formula id="scirp.72581-formula84"><graphic  xlink:href="http://html.scirp.org/file/2-7301264x2.png"  xlink:type="simple"/></disp-formula></sec><sec id="s2_7"><title>2.7. Statistical Analysis</title><p>All evaluations of antioxidant activity were performed twice. The experimental data were expressed as means &#177; standard deviation (S.D). The correlation coefficient of antioxidant activity was determined using Excel programme and Origin 6.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Hydrodistillation of dried leaves of P. lentiscus yielded 1.26%. Twenty compounds, representing 97.63% of the oil, were identified. Results of the qualitative determination of the different constituents, together with those of the quantitative analysis are compiled in <xref ref-type="table" rid="table1">Table 1</xref>. The main compounds were oxygenated monoterpenes, characterized by the great prevalence of terpinene-4-ol (41.24%) and α-terpineol (7.31%), α-pinene (9.48%), limonene (09.11%), β-myrcene (10.5 %), p-cymene (8.67 %) and α-phel-land- rene (2.20%), β-caryophyllene (22.62%) as major compounds.</p><p>As shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>, the P. lentiscus essential oil reduced the stable free radical DPPH in a concentration-dependent manner. The relationship between the antiradical activity and the concentration of Pistacia lentiscus essential oil (<xref ref-type="fig" rid="fig1">Figure 1</xref>) was positive and significant (R<sup>2</sup> = 0.995, P &lt;0.001).</p><p>The extract concentration producing 50% inhibition was calculated (<xref ref-type="fig" rid="fig1">Figure 1</xref>); it represents 0.39 mg/ml, corresponding to 0.05 mg/mL ascorbic acid (data not shown).</p></sec><sec id="s4"><title>4. Discussion</title><p>These results show that Pistacia lentiscus is rich in oxygenated monoterpene.</p><p>To the best of our knowledge this work is therefore the first report on the essential oil of Pistacia lentiscus from Oran Algeria.</p><p>In other countries of the Mediterranean region, several studies have been studied the chemical composition of P. lentiscus L. oil [<xref ref-type="bibr" rid="scirp.72581-ref6">6</xref>] - [<xref ref-type="bibr" rid="scirp.72581-ref20">20</xref>] and several compositions were observed. Myrcene (39.2%), which is the major compounds of our essential oil, has also the abundant compound in the samples from Morocco (38%) [<xref ref-type="bibr" rid="scirp.72581-ref4">4</xref>] , France (76.9%) [<xref ref-type="bibr" rid="scirp.72581-ref6">6</xref>] , Spain (27%) [<xref ref-type="bibr" rid="scirp.72581-ref7">7</xref>] , Italy (25.2%) [<xref ref-type="bibr" rid="scirp.72581-ref8">8</xref>] and Algeria (23.0% - 33.1%) [<xref ref-type="bibr" rid="scirp.72581-ref9">9</xref>] .</p><p>On the other hand, α-pinene was the major compound of the essential oils from Morocco (16.1% - 38.5%) [<xref ref-type="bibr" rid="scirp.72581-ref10">10</xref>] , Algeria (20.0% - 34.2% and 19%) [<xref ref-type="bibr" rid="scirp.72581-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.72581-ref19">19</xref>] , Tunisia (16.8%) [<xref ref-type="bibr" rid="scirp.72581-ref11">11</xref>] , Greece (24.9% - 9.4%) [<xref ref-type="bibr" rid="scirp.72581-ref12">12</xref>] , Italy (14.8% - 22.6% and 18%) [<xref ref-type="bibr" rid="scirp.72581-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.72581-ref14">14</xref>] , Spain (13.0%) [<xref ref-type="bibr" rid="scirp.72581-ref15">15</xref>] and France (31.9%) [<xref ref-type="bibr" rid="scirp.72581-ref6">6</xref>] .</p><p>In our study terpinene-4-ol was by far the major component (41.24%) accompanied</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Percentage of essential oil composition of P. lentiscus</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Peak number</th><th align="center" valign="middle" >Compound</th><th align="center" valign="middle" >Kovats index</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >α-pinene</td><td align="center" valign="middle" >928</td><td align="center" valign="middle" >9.48</td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >β-Myrcene</td><td align="center" valign="middle" >948</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >α-phellandrene</td><td align="center" valign="middle" >964</td><td align="center" valign="middle" >2.20</td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >β-pinene</td><td align="center" valign="middle" >966</td><td align="center" valign="middle" >t</td></tr><tr><td align="center" valign="middle" >5</td><td align="center" valign="middle" >Cis-ocimene</td><td align="center" valign="middle" >976</td><td align="center" valign="middle" >t</td></tr><tr><td align="center" valign="middle" >6</td><td align="center" valign="middle" >Unknow</td><td align="center" valign="middle" >998</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >7</td><td align="center" valign="middle" >3-carene</td><td align="center" valign="middle" >1005</td><td align="center" valign="middle" >0.8</td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >δ-Carene</td><td align="center" valign="middle" >1012</td><td align="center" valign="middle" >t</td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >Limonene</td><td align="center" valign="middle" >1018</td><td align="center" valign="middle" >09.11</td></tr><tr><td align="center" valign="middle" >9</td><td align="center" valign="middle" >p-Cymene</td><td align="center" valign="middle" >1028</td><td align="center" valign="middle" >8.67</td></tr><tr><td align="center" valign="middle" >10</td><td align="center" valign="middle" >p-cymen-8-ol</td><td align="center" valign="middle" >1042</td><td align="center" valign="middle" >t</td></tr><tr><td align="center" valign="middle" >11</td><td align="center" valign="middle" >Terpinolene</td><td align="center" valign="middle" >1052</td><td align="center" valign="middle" >t</td></tr><tr><td align="center" valign="middle" >12</td><td align="center" valign="middle" >Linalool</td><td align="center" valign="middle" >1082</td><td align="center" valign="middle" >1.4</td></tr><tr><td align="center" valign="middle" >13</td><td align="center" valign="middle" >Verbenol</td><td align="center" valign="middle" >1122</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >14</td><td align="center" valign="middle" >Terpinene-4-ol</td><td align="center" valign="middle" >1137</td><td align="center" valign="middle" >41.24</td></tr><tr><td align="center" valign="middle" >15</td><td align="center" valign="middle" >Borneol</td><td align="center" valign="middle" >1138</td><td align="center" valign="middle" >0.8</td></tr><tr><td align="center" valign="middle" >16</td><td align="center" valign="middle" >α-terpineol</td><td align="center" valign="middle" >1174</td><td align="center" valign="middle" >7.31</td></tr><tr><td align="center" valign="middle" >17</td><td align="center" valign="middle" >2-Undecanone</td><td align="center" valign="middle" >1290</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >18</td><td align="center" valign="middle" >Isoledene</td><td align="center" valign="middle" >1419</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >19</td><td align="center" valign="middle" >Unknow</td><td align="center" valign="middle" >1458</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >20</td><td align="center" valign="middle" >β-caryophyllene</td><td align="center" valign="middle" >1494</td><td align="center" valign="middle" >12.62</td></tr><tr><td align="center" valign="middle" >22</td><td align="center" valign="middle" >Globulol</td><td align="center" valign="middle" >1530</td><td align="center" valign="middle" >0.8</td></tr></tbody></table></table-wrap><p>Components are arranged in order of MFE1 elution, t: trace percentage (%) ≤ 0.6.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Positive correlation between the reduction of DPPH stable radical and the concentration of Pistacia lentiscus essential oil</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-7301264x3.png"/></fig><p>by limonene (09.11%), β-myrcene (10.5 %) and β-caryophyllene (12.62%). it is worth noting that this oil is the richest source of naturally occurring terpinene-4-o that has been found.</p><p>Besides, terpinen-4-ol was mainly present in the oils from Morocco (14.5% - 19.3%) [<xref ref-type="bibr" rid="scirp.72581-ref10">10</xref>] , Algeria (17.3% - 34.7%) [<xref ref-type="bibr" rid="scirp.72581-ref16">16</xref>] , Turkey (30.0% and 29.2%) [<xref ref-type="bibr" rid="scirp.72581-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.72581-ref18">18</xref>] , and France (25.6%) [<xref ref-type="bibr" rid="scirp.72581-ref6">6</xref>] . Other chemotypes were also reported: longifolene (16.4% - 12.8% Algeria) [<xref ref-type="bibr" rid="scirp.72581-ref19">19</xref>] limonene (47.0% France and 44% - 29% Algeria) [<xref ref-type="bibr" rid="scirp.72581-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.72581-ref9">9</xref>] ; β-caryophellene (19.3% - 13.1% Algeria [<xref ref-type="bibr" rid="scirp.72581-ref9">9</xref>] and 31.5% Italy [<xref ref-type="bibr" rid="scirp.72581-ref20">20</xref>] .</p><p>The antioxidant activity of Pistacia lentiscus essential oil may provide a protective effect from oxidative stress-related diseases.</p><p>As a result, the antioxidant activity of the essential oil was generally ascribed to the terpenes.</p></sec><sec id="s5"><title>5. Conclusion</title><p>In conclusion, essential oil from Pistacia lentiscus and its components generally displayed strong antioxidant properties, which are useful in daily life in foods and as preventive agents against various diseases.</p></sec><sec id="s6"><title>Cite this paper</title><p>Abdelkader, H., Nadia, K. and Salima, B. (2016) Chemical Composition and Antioxidant Potential of Pistacia lentiscus L. Essential Oil from Oran (Algeria). Advances in Bioscience and Biotechnology, 7, 539-544. http://dx.doi.org/10.4236/abb.2016.712048</p></sec></body><back><ref-list><title>References</title><ref id="scirp.72581-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ramos, A., Visozo, A., Piloto, J., Garcia, A. and Rodriguez, C.A. (2003) Screening of Antimutagenicity via Antioxidant Activity in Cuba Medicinal Plants. 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