<?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">PP</journal-id><journal-title-group><journal-title>Pharmacology &amp; Pharmacy</journal-title></journal-title-group><issn pub-type="epub">2157-9423</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/pp.2018.912039</article-id><article-id pub-id-type="publisher-id">PP-89059</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Chemistry&amp;Materials Science</subject><subject> Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Antidepressant-Like Activity of Methanolic Extract of the Seeds of &lt;i&gt;Trachysperum ammi&lt;/i&gt; in Swiss Albino Mice
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Md.</surname><given-names>Rashidur Rahman</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>Mohammad</surname><given-names>Ali</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>Mostakim</surname><given-names>Sharif</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>Sadiur</surname><given-names>Rahman Sajon</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>Md.</surname><given-names>Abdul Mannan</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>Md.</surname><given-names>Shahed-Al-Mahmud</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Pharmacy, Stamford University Bangladesh, Dhaka, Bangladesh</addr-line></aff><aff id="aff3"><addr-line>Department of Microbiology and Immunology, School of Medicine, Tzu Chi University, Hualian, Taiwan</addr-line></aff><aff id="aff1"><addr-line>Department of Pharmacy, Jessore University of Science and Technology, Jessore, Bangladesh</addr-line></aff><pub-date pub-type="epub"><day>07</day><month>12</month><year>2018</year></pub-date><volume>09</volume><issue>12</issue><fpage>503</fpage><lpage>514</lpage><history><date date-type="received"><day>6,</day>	<month>November</month>	<year>2018</year></date><date date-type="rev-recd"><day>7,</day>	<month>December</month>	<year>2018</year>	</date><date date-type="accepted"><day>10,</day>	<month>December</month>	<year>2018</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>
 
 
   
   Trachysperum ammi 
   has been traditionally used for the treatment of neurological disorders such as depression and anxiety. To date, T. ammi has reported for its chemical constituents in different diseases condition. The traditional evidence convinced us to perform the antidepressant-like activity of methanolic extract of Trachysperum ammi (META). The antidepressant activity of META assessed by using forced swimming test (FST), tail suspension test (TST), and locomotor activity test. The seed parts of META at doses level of 50, 100 and 200 mg/kg body weight administered orally to examine the CNS stimulants activity test in mice behavioral models. Here, we reported that META significantly reduced immobility time in the FST after repeated administration of 50, 100 and 200 mg/kg to mice for 14 days.
    
   The intensity of immobility significantly reduced at all of the doses (p &lt; 0.05) whereas, we were found the strongest effect observed at 200 mg/kg. The antidepressant-like effect of META caused the reduction (p &lt; 0.05) in the immobility in TST of mice when orally administered with 50, 100 and 200
    
   mg/kg for 14 days, respectively. Additionally, we were executed locomotor activity test to check the motor stimulating activity. META has employed at a dosage of 50, 100 and 200 mg/kg for 14 days, the results 
   have 
   found that 50 mg/kg produced the locomotion effects as similar to the control group. Interestingly, the locomotion, rearing, and defecation significantly
    
   (p &lt; 0.05) increased at the dosage of 100 and 200 mg/kg of META. Our present findings suggest that the seed parts of Trachysperum
    ammi
    may possess antidepressant-like activity which may use as a supportive treatment to management of neurological disorders. 
  
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Trachysperum ammi&lt;/i&gt;</kwd><kwd> Antidepressant</kwd><kwd> CNS Stimulants</kwd><kwd> Forced Swimming</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Mental depression is a chronic mental disorder that distresses a person’s mood, thoughts, physical health, and behavior. Combinations of biological and emotional components associated with depression. Retardation of thought, action, and appetite are biological symptoms &amp; emotional indicators include mystery, apathy and pessimism, low self-esteem consisting of feeling of guilt, inadequacy, and ugliness, indecisiveness, and loss of motivation [<xref ref-type="bibr" rid="scirp.89059-ref1">1</xref>] . World Health Report showed evidence that about 450 million people all over the world suffer from mental or behavioral syndrome [<xref ref-type="bibr" rid="scirp.89059-ref2">2</xref>] . It indicates about 12.3% of the worldwide burden of disease, and it may rise at 15% percent rate in 2020 [<xref ref-type="bibr" rid="scirp.89059-ref3">3</xref>] . Patients with major depressive disorder have symptoms that reflect changes in brain, monoamine neurotransmitters, specifically norepinephrine, serotonin, dopamine [<xref ref-type="bibr" rid="scirp.89059-ref4">4</xref>] . It anticipated that in 2020, after cardiovascular disease, depression may place at the second greatest increase rate of morbidity as a socioeconomic burden [<xref ref-type="bibr" rid="scirp.89059-ref5">5</xref>] . The number of drugs is available for treatment against depression, however, those drugs possess some serious side effects such as dry mouth, fatigue, gastrointestinal and respiratory problems, anxiety, agitation, drowsiness as well as cardiac arrhythmias [<xref ref-type="bibr" rid="scirp.89059-ref6">6</xref>] . Medicinal plants create an opportunity for alternative treatment for depression [<xref ref-type="bibr" rid="scirp.89059-ref7">7</xref>] . Drugs of natural origin are considered as safer and less complicated than synthetic drugs [<xref ref-type="bibr" rid="scirp.89059-ref8">8</xref>] . The aim of this study was to find out a new antidepressant drug from the natural origin.</p><p>Trachyspermum ammi is grown in the natural of Egypt and cultivated in Iraq, Iran, Afghanistan, Pakistan, and India. T. ammi L. belongs to family Apiaceae which is a highly valued medicinally important seed spice. The seed contains 2% - 4.4% brown colored oil known as ajwain oil. The main component of this oil is thymol. The oil exhibits fungicidal [<xref ref-type="bibr" rid="scirp.89059-ref9">9</xref>] , antimicrobial [<xref ref-type="bibr" rid="scirp.89059-ref10">10</xref>] , and anti-inflammatory effects on humans. It plays an important role as remedial agent for flatulence, atonic dyspepsia, and diarrhea [<xref ref-type="bibr" rid="scirp.89059-ref11">11</xref>] . It also cures abdominal tumors, abdominal pains, and piles. T. ammi has been shown to possess hypolipidemic [<xref ref-type="bibr" rid="scirp.89059-ref12">12</xref>] , digestive stimulant [<xref ref-type="bibr" rid="scirp.89059-ref13">13</xref>] , antihypertensive, hepatoprotective, antispasmodic, bronchodilator [<xref ref-type="bibr" rid="scirp.89059-ref14">14</xref>] , anti-lithiasis, diuretic [<xref ref-type="bibr" rid="scirp.89059-ref15">15</xref>] , abortifacient [<xref ref-type="bibr" rid="scirp.89059-ref16">16</xref>] , galactogogic [<xref ref-type="bibr" rid="scirp.89059-ref17">17</xref>] , antiplatelet-aggregator, antitussive [<xref ref-type="bibr" rid="scirp.89059-ref18">18</xref>] , anti-filarial [<xref ref-type="bibr" rid="scirp.89059-ref19">19</xref>] , gastroprotective [<xref ref-type="bibr" rid="scirp.89059-ref20">20</xref>] , nematicidal [<xref ref-type="bibr" rid="scirp.89059-ref21">21</xref>] , anthelmintic [<xref ref-type="bibr" rid="scirp.89059-ref22">22</xref>] , detoxification of aflatoxins [<xref ref-type="bibr" rid="scirp.89059-ref23">23</xref>] , and ameliorative effects [<xref ref-type="bibr" rid="scirp.89059-ref24">24</xref>] . Thymol also used in toothpaste and perfumery [<xref ref-type="bibr" rid="scirp.89059-ref9">9</xref>] . Seeds of T. ammi are used traditionally in Lebanon as anti-rheumatic. Fixed oil from the seed contains resin acids, palmitic acid, petroselenic acid, oleic acid and linoleic acid [<xref ref-type="bibr" rid="scirp.89059-ref25">25</xref>] .</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Plant Material Collection and Extraction</title><p>The seed of Trachysperum ammi was collected from the local market of Jessore, Bangladesh. A herbarium sheet was prepared of that sample and sent for identification and authentication which was done by a Senior Scientific Officer at Bangladesh National Herbarium, Dhaka, Bangladesh. About 500 g of seeds powdered by using mortar-pestle and was dissolved in 750 mL of methanol. The powdered material was dissolved in methanol for 72 h in a beaker and mixture was stirred every 18 h using a sterile glass rod. Room temperature also carefully maintained at 25˚C &#177; 2˚C. The desire filtrate obtained after 3 times repetition by using the Whatman No. 1 filter paper and sterilized cotton filter. Filtrated solvent evaporates by the rotary evaporator; the percentage of yield of extract was 4.80%.</p></sec><sec id="s2_2"><title>2.2. Experimental Animals</title><p>Swiss Albino mice of both sex (20 - 25 g) collected from the Animal Husbandry of Jahangirnagar University, Dhaka, Bangladesh. Animals were maintained under standard environmental conditions (temperature: 25˚C &#177; 2˚C, relative humidity: 55% - 65% and 12 h light/dark cycle). During acclimatization period, food pellets provided to the mice with fresh water and libitum. The animals allowed acclimatizing to the laboratory condition for 14 days before experimental treatment. All the experimental animals treated following the Ethical Principles and Guidelines for Scientific Experiments on Animals (1995) formulated by the Swiss Academy of Medical Sciences and the Swiss Academy of Sciences. All the experimental animals were treated following the Ethical Principles and Guidelines for Scientific Experiments on Animals formulated by Ethical Review Committee, Faculty of Biological Sciences &amp; Technology, Jessore University of Science &amp; Technology (Ref: ERC/FBS/JUST/2017-02).</p></sec><sec id="s2_3"><title>2.3. Drugs and Treatments</title><p>Imipramine hydrochloride (Sandoz, Novartis Bangladesh Ltd) used as the reference drug or positive control in antidepressant-like activity tests. All animals housed in a controlled room (temperature, 25˚C &#177; 1˚C; humidity, 45% - 50%; light-dark cycle, 12 h each). Mice were divided randomly into control, positive control, and three experimental groups. Each group contained 5 mice and treated Deionized water 0.1 ml/mice, Imipramine HCl (30 mg/kg), META (50 mg/kg), META (100 mg/kg), and META (200 mg/kg) respectively. Test solutions were administered orally using oral gavage once daily between 1-3 p.m. over a period of 14 days. All the experiments of these investigations were carried out at the Pharmacology Laboratory of the Department of Pharmacy, Jessore University of Science &amp; Technology, Bangladesh.</p></sec><sec id="s2_4"><title>2.4. Experimental Methods</title><sec id="s2_4_1"><title>2.4.1. Forced Swimming Test (FST)</title><p>FST performed according to the method which described by Porsolt et al., (1977) with some modifications [<xref ref-type="bibr" rid="scirp.89059-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.89059-ref27">27</xref>] . Animals exposed to a situation of forced swimming that based on behavioral despair, in which their movements reduced after a period of vigorous activity (struggling). However, the movements of swimming required to keep their heads above the water. Experimental mice placed in an acrylic cylinder (45 cm height = 20 cm diameter) filled with water at 25˚C &#177; 1˚C to a depth of 17 cm. According to above-mentioned apparatus, a trial session carried out (14-day treatment) which allowed the mice to swim for 15 minutes. Mouse considered immobile if it remained floating in the water, except for small movements to keep its head above the water. The FST performed between 1-3 p.m. and recorded using a video camera. The tapes evaluated by observers not informed about the kind of treatment each animal had received [<xref ref-type="bibr" rid="scirp.89059-ref28">28</xref>] .</p></sec><sec id="s2_4_2"><title>2.4.2. Tail Suspension Test (TST)</title><p>This test was performed according to the method described by Steru et al., (1985) [<xref ref-type="bibr" rid="scirp.89059-ref29">29</xref>] with slight modifications. TST is simple, reliable, and widely accepted behavioral despair model as well as screening antidepressant effect. TST involves suspending the tail of the mice upside down which shows the state of agitation and immobility as well this reflects a state of depression. TST apparatus contains two stands, each with a clamp located 22 cm from the floor, were placed at intervals of 23 cm. Each mouse was hung 5 cm from the end of its tail on a stand and recorded with a video camera for 6 min. The TST performed between 1-3 p.m. Immobility time was evaluated by observers.</p></sec><sec id="s2_4_3"><title>2.4.3. Measurement of Locomotors Activity Test (MLAT)</title><p>The locomotor activity test performed according to the method of Carlini et al., (1986) [<xref ref-type="bibr" rid="scirp.89059-ref30">30</xref>] with some modifications. A mouse placed in an open field apparatus composed of an arena 40 cm in diameter divided into 64 approximately equal areas. During open field observations, each mouse individually placed in the center of the arena 15 h after the last treatment. Following behavioral parameters observed: locomotion (number of line crossings), rearing frequencies (number of times seen standing on hind legs), and number of defecations within 5 min. Open field observations performed between 8-10 a.m.</p></sec></sec><sec id="s2_5"><title>2.5. Statistical Analysis</title><p>Statistical analysis of the experimental data performed using SPSS 23.0 version software. The statistical analysis was done by one-way analysis of variance (ANOVA) followed by Dunnett’s post hoc test. The results presented as mean value &#177; SEM (n = 5). The difference between the group was considered significant at a level of p* &lt; 0.05. The statistically significant results marked with a star (*) sign in the table as well as in the graph.</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Forced Swimming Test (FST)</title><p>The META at doses level of 50, 100 and 200 mg/kg body weight on forced swimming test in mice observed (<xref ref-type="table" rid="table1">Table 1</xref>). The extracts of T. ammi significantly reduced the immobility time in FST. Interestingly, T. ammi reduced the immobility time notable at 200 mg/kg when compared with the control group (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Imipramine HCl also showed the same antidepressant manner.</p></sec><sec id="s3_2"><title>3.2. Tail Suspension Test (TST)</title><p>The META at doses level of 50, 100 and 200 mg/kg body weight on tail suspension in mice showed the positive result (<xref ref-type="table" rid="table2">Table 2</xref>). The immobility time in the TST using mice markedly reduced after acute 14 days treatment with Imipramine HCl (30 mg/kg). Administration of extracts of T. ammi at dosages of 50, 100, and 200 mg/kg significantly reduced the immobility time (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p></sec><sec id="s3_3"><title>3.3. Measurement of Locomotor Activity Test (MLAT)</title><p>The META at doses level of 50, 100 and 200 mg/kg body weight on the measurement of locomotor activity test in mice observed. The extracts of T. ammi (50 mg/kg) shown that the same locomotion effect of the control group (<xref ref-type="table" rid="table3">Table 3</xref>). However, 100 mg/Kg and 200 mg/kg doses of T. ammi shown the significant increase of locomotion, rearing, and defecation. All the test animals compared with positive control (Figures 3(a)-3(c)).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Effect of META in forced swimming test on mice</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Treatment</th><th align="center" valign="middle" >Doses</th><th align="center" valign="middle" >Immobility time</th></tr></thead><tr><td align="center" valign="middle" >Deionized water</td><td align="center" valign="middle" >0.1 ml/mice</td><td align="center" valign="middle" >106.20 &#177; 17.890</td></tr><tr><td align="center" valign="middle" >Imipramine Hydrochloride</td><td align="center" valign="middle" >30 mg/kg</td><td align="center" valign="middle" >18.50 &#177; 3.403*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >50 mg/kg</td><td align="center" valign="middle" >46.25 &#177; 5.250*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >100 mg/kg</td><td align="center" valign="middle" >41.0 &#177; 2.121*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >200 mg/kg</td><td align="center" valign="middle" >31.80 &#177; 7.479*</td></tr></tbody></table></table-wrap><p>Values are presented as mean &#177; SEM, where n = 5. Control = Distilled water, 0.1 ml/mice, Imipramine HCl = 30 mg/kg, Group META = 50, 100 and 200 mg/kg body weight. *p &lt; 0.05 compared with the control group (Dunnett’s test).</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Effect of META in tail suspension test on mice</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Treatment</th><th align="center" valign="middle" >Doses</th><th align="center" valign="middle" >Immobility time</th></tr></thead><tr><td align="center" valign="middle" >Deionized water</td><td align="center" valign="middle" >0.1 ml/mice</td><td align="center" valign="middle" >105.87 &#177; 1.612</td></tr><tr><td align="center" valign="middle" >Imipramine Hydrochloride</td><td align="center" valign="middle" >30 mg/kg</td><td align="center" valign="middle" >17.25 &#177; 2.750*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >50 mg/kg</td><td align="center" valign="middle" >51.25 &#177; 9.690*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >100 mg/kg</td><td align="center" valign="middle" >34.25 &#177; 5.677*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >200 mg/kg</td><td align="center" valign="middle" >28.4 &#177; 2.293*</td></tr></tbody></table></table-wrap><p>Values are presented as mean &#177; SEM, where n = 5. Control = Distilled water, 0.1 ml/mice, Imipramine HCl = 30 mg/kg, Group META = 50, 100 and 200 mg/kg body weight. *p &lt; 0.05 compared with the control group (Dunnett’s test).</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Effect of META in locomotor activity test on mice</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Treatment</th><th align="center" valign="middle" >Doses</th><th align="center" valign="middle" >Locomotion</th><th align="center" valign="middle" >Rearing</th><th align="center" valign="middle" >Defecation</th></tr></thead><tr><td align="center" valign="middle" >Deionized water</td><td align="center" valign="middle" >0.1 ml/mice</td><td align="center" valign="middle" >94.0 &#177; 3.768</td><td align="center" valign="middle" >16.2 &#177; 4.841</td><td align="center" valign="middle" >0.80 &#177; 0.583</td></tr><tr><td align="center" valign="middle" >Imipramine Hydrochloride</td><td align="center" valign="middle" >30 mg/kg</td><td align="center" valign="middle" >206.25 &#177; 10.0*</td><td align="center" valign="middle" >37.75 &#177; 1.75*</td><td align="center" valign="middle" >3.25 &#177; 0.25*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >50 mg/kg</td><td align="center" valign="middle" >118.2 &#177; 9.903</td><td align="center" valign="middle" >21 &#177; 1.472</td><td align="center" valign="middle" >2.00 &#177; 0.408</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >100 mg/kg</td><td align="center" valign="middle" >159.5 &#177; 7.963*</td><td align="center" valign="middle" >26.5 &#177; 0.866*</td><td align="center" valign="middle" >2.25 &#177; 0.25*</td></tr><tr><td align="center" valign="middle" >META</td><td align="center" valign="middle" >200 mg/kg</td><td align="center" valign="middle" >177.2 &#177; 28.34*</td><td align="center" valign="middle" >34.2 &#177; 1.655*</td><td align="center" valign="middle" >3.00 &#177; 0.316*</td></tr></tbody></table></table-wrap><p>Values are presented as mean &#177; SEM, where n = 5. Control = Distilled water, 0.1 ml/mice, Imipramine HCl = 30 mg/kg, Group META = 50, 100 and 200 mg/kg body weight. *p &lt; 0.05 compared with the control group (Dunnett’s test).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Many of the plants used as crude extracts and purified natural products [<xref ref-type="bibr" rid="scirp.89059-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.89059-ref32">32</xref>] which have potential medicinal properties [<xref ref-type="bibr" rid="scirp.89059-ref33">33</xref>] . The aimed of our present study to evaluate the antidepressant-like effects of methanolic extract of the seeds of T. ammi using behavioral animal models. Our present study indicates that the antidepressant-like effect of META found to compare with the standard drug Imipramine hydrochloride (30 mg/kg). Imipramine hydrochloride acts by inhibiting norepinephrine reuptake and has used as a standard drug in majority studies. Rodents displayed immobility when unavoidable stress subjected such as forced swimming is thought to reflect a state of despair or lowered mood. This condition reflects depressive disorders in humans. Additionally, the antidepressant drugs treatment reduced the immobility time. Moreover, a significant correlation found between the clinical efficacy of antidepressant drugs and their potency in this model. In the present study, META significantly reduced immobility time in the FST after repeated administration of 50, 100 and 200 mg/kg to mice for 14 d. The intensity of immobility reduction was statistically significant at all doses (p* &lt; 0.05) but strongest at a dosage of 200 mg/kg.</p><p>META exhibited a reduction in the time of immobility at the dose of 50 and 100 mg/kg. Interestingly, 200 mg/kg was produced the higher reduction of immobility compared with the control group. The efficacy of immobility decreased in the FST &amp; TST which may occur with psycho-stimulants, exert an indiscriminate motor stimulating activity [<xref ref-type="bibr" rid="scirp.89059-ref34">34</xref>] . The motor stimulating activity of META was performed with the open field test to exclude the confusion. The administration of META at a dosage of 50, 100 and 200 mg/kg for 14 d exerts statistically significant (p* &lt; 0.05) at the doses of 100 and 200 mg/kg as well as also indicates that the reduction of immobility time after 14 d administration of META attributed to an inherent antidepressant effect. Thus, the effective dosage of META in the FST seems to be around 200 mg/kg body weight.</p><p>The beneficial effect of Imipramine hydrochloride in TST model seems to be due to increased availability of these neurotransmitters (NE) and serotonin (5HT) at the postsynaptic site following reuptake inhibition [<xref ref-type="bibr" rid="scirp.89059-ref35">35</xref>] . Some researchers already have shown the adaptogenic effect of the plant extract via normalization of the various stress parameters and monoaminergic levels [<xref ref-type="bibr" rid="scirp.89059-ref36">36</xref>] . Those studies may provide a hint about extract which involved in possible antidepressant-like effect through the restoration of normal monoaminergic NE [<xref ref-type="bibr" rid="scirp.89059-ref37">37</xref>] . The action of the triterpenoid and saponins resulted in the enhancement of the nerve impulse transmission. Neurochemical assays suggested that treatment by triterpenoid and saponins improved brain antioxidant activity to varying degrees after the behavioral despair test [<xref ref-type="bibr" rid="scirp.89059-ref38">38</xref>] . The pattern of CNS effects observed through this experiment suggests us the involvement of norepinephrine NE system on its antidepressant-like effect.</p></sec><sec id="s5"><title>5. Conclusion</title><p>The findings obtained from forced swimming test (FST), tail suspension test (TST), and measurement of locomotor activity test (MLAT) clearly indicate that the methanolic extract of the seeds of Trachysperum ammi possesses a significant antidepressant-like activity. The outcome also indicates that the antidepressant-like activity observed without the involvement of non-specific motor stimulation. However, different research approach must be needed to elucidate the mechanism of action of Trachysperum ammi. The experimental findings suggest the antidepressant-like effects that may involve in norepinephrine neurotransmitters system.</p></sec><sec id="s6"><title>Ethical Approval</title><p>All procedures performed in this study involving animals were approved in accordance with the ethical standards of the Ethical Review Committee, Faculty of Biological Sciences and Technology, Jessore University of Science and Technology, Jessore, Bangladesh (Ref: ERC/FBS/JUST/2017-02).</p></sec><sec id="s7"><title>Consent for Publication</title><p>Not applicable.</p></sec><sec id="s8"><title>Availability of Data and Material</title><p>Not applicable.</p></sec><sec id="s9"><title>Funding</title><p>This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.</p></sec><sec id="s10"><title>Authors’ Contributions</title><p>Md. Rashidur Rahman designed, and supervised the experimental work. Mohammad Ali, Mostakim Sharif, and Sadiur Rahman Sajon coordinated forced swimming test, tail suspension test, and locomotor activity test and interpreted the results. Md. Abdul Mannan has done statistical analysis and drawn the graphs. Md. Shahed-Al-Mahmud drafted the manuscript. All authors read and approved the manuscript.</p></sec><sec id="s11"><title>Acknowledgements</title><p>The authors are grateful to the chairman of the department of Pharmacy, Jessore University of Science and Technology for permitting us to use the facilities of Pharmacognosy and Pharmacology Laboratory.</p></sec><sec id="s12"><title>Authors’ Information (Optional)</title><p>1 - 4 Department of Pharmacy, Jessore University of Science and Technology, Jessore, Bangladesh.</p><p>5 Department of Pharmacy, Stamford University Bangladesh, Dhaka, Bangladesh.</p><p>6 Department of Microbiology and Immunology, School of Medicine, Tzu Chi University, Hualian, Taiwan.</p>Conflicts of Interest<p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s13"><title>Cite this paper</title><p>Rahman, M.R., Ali, M., Sharif, M., Sajon, S.R., Mannan, M.A. and Shahed-Al-Mahmud, M. (2018) Antidepressant-Like Activity of Methanolic Extract of the Seeds of Trachysperum ammi in Swiss Albino Mice. Pharmacology &amp; Pharmacy, 9, 503-514. https://doi.org/10.4236/pp.2018.912039</p></sec><sec id="s14"><title>Abbreviations</title><p>META: Methanolic Extract of the seeds of Trachysperum ammi</p><p>FST: Forced Swimming Test</p><p>TST: Tail Suspension Test</p><p>NE: Neurotransmitters</p><p>Min: minutes</p></sec></body><back><ref-list><title>References</title><ref id="scirp.89059-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Keya, S.N., Shahed-Al-Mahmud, M. and Rahman, M.R. (2018) Antidepressant-Like Effects of Methanolic Extract of Xanthium strumarium (Asteraceae) in Mice. Current Trends in Biotechnology and Pharmacy, 12, 33-37.</mixed-citation></ref><ref id="scirp.89059-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">World Health Organization (2001) The World Health Report 2001: Mental Health: New Understanding, New Hope.</mixed-citation></ref><ref id="scirp.89059-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Weyand, C.M. and Goronzy, J.J. (2018) Vasculitides. Primer on the Rheumatic Diseases, 1, 398-450.</mixed-citation></ref><ref id="scirp.89059-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Gold, P.W., Goodwin, F.K. and Chrousos, G.P. (1988) Clinical and Biochemical Manifestations of Depression. New England Journal of Medicine, 319, 413-420. https://doi.org/10.1056/NEJM198808183190706</mixed-citation></ref><ref id="scirp.89059-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Hoge, C.W., Auchterlonie, J.L. and Milliken, C.S. (2006) Mental Health Problems, Use of Mental Health Services, and Attrition from Military Service after Returning from Deployment to Iraq or Afghanistan. JAMA, 295, 1023-1032. https://doi.org/10.1001/jama.295.9.1023</mixed-citation></ref><ref id="scirp.89059-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, Z.-J. (2004) Therapeutic Effects of Herbal Extracts and Constituents in Animal Models of Psychiatric Disorders. Life Sciences, 75, 1659-1699. https://doi.org/10.1016/j.lfs.2004.04.014</mixed-citation></ref><ref id="scirp.89059-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Shahed-Al-Mahmud, M. and Lina, S.M.M. (2018) Evaluation of Sedative and Anxiolytic Activities of Methanol Extract of Leaves of Persicaria hydropiper in Mice. Clinical Phytoscience, 3, 20.</mixed-citation></ref><ref id="scirp.89059-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Saha, A.K., Rahman, M.R., Shahriar, M., Saha, S.K., Al Azad, N. and Das, S. (2013) Screening of Six Ayurvedic Medicinal Plant Extracts for Antioxidant and Cytotoxic Activity. Journal of Pharmacognosy and Phytochemistry, 2, 181-188.</mixed-citation></ref><ref id="scirp.89059-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Srivastava, K. (1988) Extract of a Spice—Omum (Trachyspermum ammi)—Shows Antiaggregatory Effects and Alters Arachidonic Acid Metabolism in Human Platelets. Prostaglandins, Leukotrienes and Essential Fatty Acids, 33, 1-6. https://doi.org/10.1016/0952-3278(88)90115-9</mixed-citation></ref><ref id="scirp.89059-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Rizk, A.F.M. (1987) The Chemical Constituents and Economic Plants of the Euphorbiaceae. Botanical Journal of the Linnean Society, 94, 293-326. https://doi.org/10.1111/j.1095-8339.1987.tb01052.x</mixed-citation></ref><ref id="scirp.89059-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Warrier, P.K. and Nambiar, V. (1993) Indian Medicinal Plants: A Compendium of 500 Species. Vol. 5, Orient Blackswan.</mixed-citation></ref><ref id="scirp.89059-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Kumari, K. and Prameela, M. (1992) Effect of Incorporating Carum Copticum Seeds in a High Fat Diet for Albino Rats. Medical Science Research.</mixed-citation></ref><ref id="scirp.89059-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Vasudevan, K., Vembar, S., Veeraraghavan, K. and Haranath, P. (2000) Influence of Intragastric Perfusion of Aqueous Spice Extracts on Acid Secretion in Anesthetized Albino Rats. Indian Journal of Gastroenterology: Official Journal of the Indian Society of Gastroenterology, 19, 53-56.</mixed-citation></ref><ref id="scirp.89059-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Gilani, A., Jabeen, Q., Ghayur, M., Janbaz, K. and Akhtar, M. (2005) Studies on the Antihypertensive, Antispasmodic, Bronchodilator and Hepatoprotective Activities of the Carum copticum Seed Extract. Journal of Ethnopharmacology, 98, 127-135. https://doi.org/10.1016/j.jep.2005.01.017</mixed-citation></ref><ref id="scirp.89059-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Ahsan, S., Shah, A., Tanira, M., Ahmad, M., Tariq, M. and Ageel, A. (1990) Studies on Some Herbal Drugs Used against Kidney Stones in Saudi Folk Medicine. Fitoterapia, 61, 435-438.</mixed-citation></ref><ref id="scirp.89059-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Nath, D., Sethi, N., Srivastava, S., Jain, A. and Srivastava, R. (1997) Survey on Indigenous Medicinal Plants Used for Abortion in Some Districts of Uttar Pradesh. Fitoterapia, 68, 223-225.</mixed-citation></ref><ref id="scirp.89059-ref17"><label>17</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Kaur</surname><given-names> H. </given-names></name>,<etal>et al</etal>. (<year>1998</year>)<article-title>Estrogenic Activity of Some Herbal Galactogogue Constituents</article-title><source> Indian Journal of Animal Nutrition</source><volume> 15</volume>,<fpage> 232</fpage>-<lpage>234</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.89059-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Boskabady, M., Jandaghi, P., Kiani, S. and Hasanzadeh, L. (2005) Antitussive Effect of Carum copticum in Guinea Pigs. Journal of Ethnopharmacology, 97, 79-82. https://doi.org/10.1016/j.jep.2004.10.016</mixed-citation></ref><ref id="scirp.89059-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Mathew, N., Misra-Bhattacharya, S., Perumal, V. and Muthuswamy, K. (2008) Antifilarial Lead Molecules Isolated from Trachyspermum ammi. Molecules, 13, 2156-2168. https://doi.org/10.3390/molecules13092156</mixed-citation></ref><ref id="scirp.89059-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Ramaswamy, S., Sengottuvelu, S., Sherief, S.H., Jaikumar, S., Saravanan, R., Prasadkumar, C. and Sivakumar, T. (2010) Gastroprotective Activity of Ethanolic Extract of Trachyspermum ammi Fruit. International Journal of Pharma and Bio Sciences, 1, 1-15.</mixed-citation></ref><ref id="scirp.89059-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Pelczar, M., Chan, E. and Krieg, N. (1988) Control of Microorganisms, the Control of Microorganisms by Physical Agents. In: Microbiology, McGraw-Hill International, New York, 469-509.</mixed-citation></ref><ref id="scirp.89059-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Priestley, C.M., Williamson, E.M., Wafford, K.A. and Sattelle, D.B. (2003) Thymol, a Constituent of Thyme Essential Oil, Is a Positive Allosteric Modulator of Human GABAA Receptors and a Homo-Oligomeric GABA Receptor from Drosophila melanogaster. British Journal of Pharmacology, 140, 1363-1372. https://doi.org/10.1038/sj.bjp.0705542</mixed-citation></ref><ref id="scirp.89059-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Velazhahan, R., Vijayanandraj, S., Vijayasamundeeswari, A., Paranidharan, V., Samiyappan, R., Iwamoto, T., Friebe, B. and Muthukrishnan, S. (2010) Detoxification of Aflatoxins by Seed Extracts of the Medicinal Plant, Trachyspermum ammi (L.) Sprague ex Turrill-Structural Analysis and Biological Toxicity of Degradation Product of Aflatoxin G1. Food Control, 21, 719-725. https://doi.org/10.1016/j.foodcont.2009.10.014</mixed-citation></ref><ref id="scirp.89059-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Anilakumar, K., Saritha, V., Khanum, F. and Bawa, A. (2009) Ameliorative Effect of Ajwain Extract on Hexachlorocyclohexane-Induced Lipid Peroxidation in Rat Liver. Food and Chemical Toxicology, 47, 279-282. https://doi.org/10.1016/j.fct.2008.09.061</mixed-citation></ref><ref id="scirp.89059-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Nelly, A., Annick, D.-D. and Frederic, D. (2008) Plants Used as Remedies Antirheumatic and Antineuralgic in the Traditional Medicine of Lebanon. Journal of Ethnopharmacology, 120, 315-334. https://doi.org/10.1016/j.jep.2008.08.024</mixed-citation></ref><ref id="scirp.89059-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Porsolt, R., Le Pichon, M. and Jalfre, M. (1977) Depression: A New Animal Model Sensitive to Antidepressant Treatments. Nature, 266, 730. https://doi.org/10.1038/266730a0</mixed-citation></ref><ref id="scirp.89059-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Porsolt, R., Bertin, A. and Jalfre, M. (1977) Behavioral Despair in Mice: A Primary Screening Test for Antidepressants. Archives Internationales de Pharmacodynamie et de Therapie, 229, 327-336.</mixed-citation></ref><ref id="scirp.89059-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Sakakibara, H., Ishida, K., Grundmann, O., Nakajima, J.-I., Seo, S., Butterweck, V., Minami, Y., Saito, S., Kawai, Y. and Nakaya, Y. (2006) Antidepressant Effect of Extracts from Ginkgo biloba Leaves in Behavioral Models. Biological and Pharmaceutical Bulletin, 29, 1767-1770. https://doi.org/10.1248/bpb.29.1767</mixed-citation></ref><ref id="scirp.89059-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Steru, L., Chermat, R., Thierry, B. and Simon, P. (1985) The Tail Suspension Test: A New Method for Screening Antidepressants in Mice. Psychopharmacology, 85, 367-370. https://doi.org/10.1007/BF00428203</mixed-citation></ref><ref id="scirp.89059-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Carlini, E.A., Contar, J.D.D., Silva-Filho, A.R., Da Silveira-Filho, N.G., Frochtengarten, M.L. and Bueno, O.F. (1986) Pharmacology of Lemongrass (Cymbopogon citratus Stapf). I. Effects of Teas Prepared from the Leaves on Laboratory Animals. Journal of Ethnopharmacology, 17, 37-64. https://doi.org/10.1016/0378-8741(86)90072-3</mixed-citation></ref><ref id="scirp.89059-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Shahed-Al-Mahmud, M., Jahan, T. and Islam, M.T. (2018) Antidiarrheal Activities of Hydroalcoholic Extract of Sida cordifolia Roots in Wister Albino Rats. Oriental Pharmacy and Experimental Medicine, 18, 51-58. https://doi.org/10.1007/s13596-017-0295-5</mixed-citation></ref><ref id="scirp.89059-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Shahed-Al-Mahmud, M., Shawon, M.J.A., Islam, T., Rahman, M.M. and Rahman, M.R. (2018) In Vivo Anti-Diarrheal Activity of Methanolic Extract of Streblus asper Leaves Stimulating the Na+/K+-ATPase in Swiss Albino Rats. Indian Journal of Clinical Biochemistry, 1-8.</mixed-citation></ref><ref id="scirp.89059-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Sarwar, S., Rahman, M.R., Nahar, K. and Rahman, M.A. (2014) Analgesic and Neuropharmacological Activities of Methanolic Leaf Extract of Clitoria ternatea Linn. Journal of Pharmacognosy and Phytochemistry, 2, 110-114.</mixed-citation></ref><ref id="scirp.89059-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Mannan, A., Abir, A.B. and Rahman, R. (2015) Antidepressant-Like Effects of Methanolic Extract of Bacopa monniera in Mice. BMC Complementary and Alternative Medicine, 15, 337. https://doi.org/10.1186/s12906-015-0866-2</mixed-citation></ref><ref id="scirp.89059-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Vergura, R., Balboni, G., Spagnolo, B., Gavioli, E., Lambert, D.G., McDonald, J., Trapella, C., Lazarus, L.H., Regoli, D. and Guerrini, R. (2008) Anxiolytic- and Antidepressant-Like Activities of H-Dmt-Tic-NH-CH (CH2-COOH)-Bid (UFP-512), a Novel Selective Delta Opioid Receptor Agonist. Peptides, 29, 93-103. https://doi.org/10.1016/j.peptides.2007.10.012</mixed-citation></ref><ref id="scirp.89059-ref36"><label>36</label><mixed-citation publication-type="other" xlink:type="simple">Ismail, H., Amanat, M.A., Iqbal, A. and Mirza, B. (2018) Medicinal Plants: A Complementary and Alternative Antidepressant Therapy. Current Pharmaceutical Design, 24, 2609-2624. https://doi.org/10.2174/1381612824666180727123950</mixed-citation></ref><ref id="scirp.89059-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Abouhosseini Tabari, M., Hajizadeh Moghaddam, A., Maggi, F. and Benelli, G. (2018) Anxiolytic and Antidepressant Activities of Pelargonium roseum Essential Oil on Swiss Albino Mice: Possible Involvement of Serotonergic Transmission. Phytotherapy Research, 32, 1014-1022. https://doi.org/10.1002/ptr.6038</mixed-citation></ref><ref id="scirp.89059-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Prasad, R., Kamal, S., Sharma, P.K., Oelmüller, R. and Varma, A. (2013) Root Endophyte Piriformospora indica DSM 11827 Alters Plant Morphology, Enhances Biomass and Antioxidant Activity of Medicinal Plant Bacopa monniera. Journal of Basic Microbiology, 53, 1016-1024. https://doi.org/10.1002/jobm.201200367</mixed-citation></ref></ref-list></back></article>