<?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">OJAppS</journal-id><journal-title-group><journal-title>Open Journal of Applied Sciences</journal-title></journal-title-group><issn pub-type="epub">2165-3917</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojapps.2021.1112097</article-id><article-id pub-id-type="publisher-id">OJAppS-113940</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> Chemistry&amp;Materials Science</subject><subject> Computer Science&amp;Communications</subject><subject> Engineering</subject><subject> Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  In &lt;i&gt;Vitro&lt;/i&gt; Anthelmintic Activity of Leaf Extracts of &lt;i&gt;Celosia&lt;/i&gt; laxa Schum. &amp; Thonn
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sylvester</surname><given-names>Nefai Mathias</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>Emmanuel</surname><given-names>Halilu Mshelia</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>Bala</surname><given-names>Bilyaminu Danbala</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>Aminu</surname><given-names>Ahmed Biambo</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Department of Clinical and Pharmacy Practice, Faculty of Pharmaceutical Sciences, Usmanu Danfodiyo University, Sokoto, Nigeria</addr-line></aff><aff id="aff2"><addr-line>Faculty of Pharmacy, Cyprus International University, Haspolat/Nicosia, Mersin, Turkey</addr-line></aff><aff id="aff1"><addr-line>Department of Pharmacognosy and Ethnopharmacy, Usmanu Danfodiyo University, Sokoto, Nigeria</addr-line></aff><pub-date pub-type="epub"><day>15</day><month>12</month><year>2021</year></pub-date><volume>11</volume><issue>12</issue><fpage>1277</fpage><lpage>1286</lpage><history><date date-type="received"><day>19,</day>	<month>October</month>	<year>2021</year></date><date date-type="rev-recd"><day>14,</day>	<month>December</month>	<year>2021</year>	</date><date date-type="accepted"><day>17,</day>	<month>December</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:
   Celosia laxa (Amaranthaceae) is mainly a west African plant species used in Traditional Medicine as an anthelmintic, anticancer, antibacterial and analgesic agent. The seeming prevalence of worm infection in Gwandu 
  community of Gwandu Local Government Area of Kebbi State-Nigeria
   prompted this study. <b>Methods:</b> Whole plant of C. laxa extracts obtained through maceration in aqueous (AE), methanol (ME) and hexane (HE) solvents were investi
  gated for their anthelmintic activity against Indian earthworms (Pheretima posthuman) at four different (gradient) concentrations of 10, 20, 40 and 80 (mg/ml) for each extract. The study involved the determination of time of paralysis (P) and time of death (D) of the worms. <b>Results:</b> Both the aqueous and ethanolic extracts exhibited significant anthelmintic activity at the highest concentration of 80 mg/ml as compared to the standard drug, praziquantel (10
   
  mg/ml). Consequently, the aqueous extract showed a higher activity at 80
   
  mg/ml compared to standard praziquantel at 10
   
  mg/ml (with no significant value of p
   
  &lt;
   
  0.05). The time of paralysis and death observed for AE was 13.0 &#177; 1.8 and 16.8 &#177; 1.5 while the ME was less bioactive with 15.7 &#177; 0.5 and 23.0 &#177; 0.0 respectively. However, on the other hand, the hexane extract recorded no-activity on all the test
   
  sample concentrations, compared
   to 
  the standard drug (with a significant difference of p-value, p
   
  &gt;
   
  0.05). <b>Conclusion:</b> It was concluded that the leaves of C. laxa 
  are
   likely to yield a potent anthelminthic drug owing to soluble phytoconstituent which are largely hydrophilicity extracted by the polar solvents. Also, considering that the plants’ mode of preparation for use by the locals was aqueous decoction before administration, the folkloric therapeutic claims can be said to have been justified.
 
</p></abstract><kwd-group><kwd>Anthelmintic</kwd><kwd> Extracts</kwd><kwd> Maceration</kwd><kwd> Praziquantel</kwd><kwd> Phytoconstituents</kwd><kwd> Indian Earthworm</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Helminth is derived from the Greek word helminths—meaning, worm. Helminth is a broad categorical term referring to various types of parasitic worms that reside in the body [<xref ref-type="bibr" rid="scirp.113940-ref1">1</xref>]. The World Health Organization reveals that over two billion people are suffering from parasitic worm infections [<xref ref-type="bibr" rid="scirp.113940-ref2">2</xref>]. It is estimated that by the year 2025, about 57% of the population in developing countries will be influenced [<xref ref-type="bibr" rid="scirp.113940-ref3">3</xref>]. Helmintic infections are very common in men. Helminthic infections can serve as a threat to human beings, especially in developing countries. It leads to malnutrition, anemia and pneumonia. Majority of the infections, which are due to worms are mostly limited to tropical regions. Anthelmintics are drugs that may act locally to expel worms from the GIT or systemically to eradicate adult helminths or development forms that invade organs and tissues [<xref ref-type="bibr" rid="scirp.113940-ref4">4</xref>].</p><p>Celosia is a small genus of edible and ornamental plants belonging to the family Amaranthaceae. Among the different species in the genus celosia, C. laxa (Plate 1) is an important tropical leafy vegetable crop of high nutritional value [<xref ref-type="bibr" rid="scirp.113940-ref5">5</xref>]. An Indian origin of C. laxa, of tropical origin is known for its very brilliant colors with a wide range of traditional uses such as treatment of mouth sores, blood diseases, diabetes mellitus and as an aphrodisiac; with also claims of cure against ovarian and uterine diseases [<xref ref-type="bibr" rid="scirp.113940-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.113940-ref7">7</xref>]. However, C. laxa is largely a west African plant species used traditionally as an anthelmintic, anticancer, antibacterial and analgesic agent. The whole plant has also been reported for use in the treatment of diarrhea, piles, bleeding nose, as a disinfectant, inflammation, haematological and gynaecologic disorders [<xref ref-type="bibr" rid="scirp.113940-ref8">8</xref>].</p><p>Locally, the Hausas call it “bokan gida” or “n&#224;nn&#225;fa&#225;”, or “n&#224;nn&#224;ho&#243;”, while in Southwestern Nigeria it is called &#224;jẹ f&#225;wo. In west Africa of Sierra leone and Gambia, it is called “gimbui” and “furayŋamo” respectively. The study was thus prompted by the fact that there was a seeming prevalence of worm infection in Gwandu community of Gwandu Local Government Area of Kebbi State-Nigeria.</p><p>Earlier interviews among the locals in the various village communities of Gwandu LGA in Kebbi State-Nigeria, revealed several cases and complains of stomach ache and parasitic diseases leading to the use of a decocted plant species of C. laxa to effect cure. Thus, the seeming prevalence of worm infection and diseases that bore similarities with the later in these communities prompted this study. Moreover, it has been reported that most of the existing anthelmintics produce side effects such as abdominal pain, loss of appetite, nausea, vomiting, headache and diarrhea [<xref ref-type="bibr" rid="scirp.113940-ref9">9</xref>].</p><p>Hence, Anthelmintics from the natural sources may play a key role in the treatment of these parasite infections [<xref ref-type="bibr" rid="scirp.113940-ref10">10</xref>]. Literature has also shown that increasing problems of development of resistance in helminths against anthelmintics have led to the proposal of screening medicinal plants for their anthelmintic activity [<xref ref-type="bibr" rid="scirp.113940-ref11">11</xref>]. Consequently, based largely on folklore therapeutic claims, the present study was carried out to assess the anthelmintic activity of Celosia laxa against Pheretima posthuma using three extracts obtained from solvents of gradient polarity.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Plant Collection and Authentication</title><p>Leaves and whole plant of celosia laxa were collected in April 2017 from Gwandu town of Kebbi State, Nigeria. It was authenticated using compendium by Rogers of the Hausa Plant-Scientific names compilations. Herbarium specimen was thereafter prepared and deposited at the Department of Pharmacognosy, Usmanu Danfodiyo University Sokoto (UDUS) with voucher number PCG/UD- US/Amar/0005.</p></sec><sec id="s2_2"><title>2.2. Worms Collection and Authentication</title><p>Pheretima posthuman was collected from the water-logged areas of the soil and identified and authenticated at the Veterinary Faculty of UDUS.</p></sec></sec><sec id="s3"><title>3. Preparation of Extract</title><sec id="s3_1"><title>3.1. Aqueous, Methanol and Hexane Extract Preparation</title><p>The crude aqueous extract of C. laxa leaves was prepared according to the standard method. One hundred grams of the powdered plant material was mixed with 500 mL of distilled water in a Soxhlet apparatus for 8 - 12 h. The filtrate was concentrated in a rotary evaporator and the extract labeled AE, was stored at 4˚C until required. Methanol extract was obtained from the dried powder (350 g) by maceration for two days in 1.7 litters of 70% methanol solvent. The extract was evaporated in vacuo to obtain a dark green residue and labeled ME. This was stored at 4˚C until use. Similarly, 350 g of powdered C. laxa plant were macerated in n-hexane solvent of 750 mL for some 18 hours, filtered and concentrated to obtained a greenish extract labeled, HE. This was stored at 4˚C until use.</p></sec><sec id="s3_2"><title>3.2. Phytochemical Evaluation</title><p>The qualitative chemical tests to detect the various phytoconstituents were carried on the extracts of C. laxa plant using the methods described by [<xref ref-type="bibr" rid="scirp.113940-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.113940-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.113940-ref14">14</xref>].</p></sec><sec id="s3_3"><title>3.3. Anthelmintic Assay</title><p>The method of [<xref ref-type="bibr" rid="scirp.113940-ref15">15</xref>] was adopted with slight modifications. Adult earthworm (Pheretimaposthuma) of uniform size was collected at water logged areas, were identified, and washed with distilled water to remove dirty matter. The worms were divided into four groups, each containing six worms. The plant extracts and standards (10 mg/mL) were poured into petri-dishes and the earthworm released. For the extracts, 100 ml formulations containing four different concentrations (10, 20, 40 and 80) mg/ml in distilled water, each of aqueous, ethanol and hexane extract, were prepared and the six worms (of same type) were placed in it.</p><p>Distilled water was used in place of plant extract for the control group. All solutions were prepared freshly before starting the assay.</p><p>Movement of the worms were monitored in terms of changes in rapid movement, the release of body exudates, segment breakage and decolorization; by observing keenly with the naked eye as well as with the aid of a hand lens magnifier. Time was noted for the death of worms, which was confirmed by immobility and fading of body colour of worms. Also, paralysis was noted by dipping non-motile worms in hot water to see for possible resurrection. Generally, time for paralysis as well as death of the worms were noted and recorded.</p></sec><sec id="s3_4"><title>3.4. Data Analysis</title><p>The result of each group of experimental animals were express as mean (%) &#177; standard error of mean (S. E. M.). Data were analyzed using one-way factorial ANOVA tests, followed by Dunnett’s t-tests on each group. P values under 0.05 were considered highly significant (shown as **).</p></sec></sec><sec id="s4"><title>4. Results</title>Preliminary Phyto-Constituent Analysis<p>Phytochemical screening of the extracts revealed richly, the presence of alkaloids, cardiac glycosides and less richly some other metabolites which are mainly polyphenolics. These are shown in <xref ref-type="table" rid="table1">Table 1</xref>. While, chemo-microscopical studies carried out on the powdered drug of C. laxa revealed the presence of fat and oil, calcium oxalate and starch as shown in <xref ref-type="table" rid="table2">Table 2</xref>.</p></sec><sec id="s5"><title>5. Discussions</title><p>All anthelmintics essentially kill worms by either starving them to death or paralyzing them because worms have no means of storing energy, they must eat almost continuously to meet their metabolic needs [<xref ref-type="bibr" rid="scirp.113940-ref17">17</xref>]. Any disruption in this process results in energy depletion. Interfering with feeding for 24 hours or less is sufficient to kill most adult parasites. Parasites will also die if they become paralyzed and temporarily lose their ability to maintain their position in the gut [<xref ref-type="bibr" rid="scirp.113940-ref18">18</xref>]. Preliminary phytochemical screening of C. laxa extract recorded on <xref ref-type="table" rid="table1">Table 1</xref> revealed the presence of proteins, saponins, steroids, carbohydrates, alkaloids, tannins, glycosides, flavonoids and phenols. Phytochemical qualitative test performed from earlier study of same plant conformed with this result [<xref ref-type="bibr" rid="scirp.113940-ref19">19</xref>].</p><p>Phenolic anthelmintics interfere with the energy generation in the helminth parasites by uncoupling the oxidative phosphorylation. Another possible mechanism of action is that they bind to free proteins in the gastrointestinal tract of the host animal or to glycoprotein on the cuticle of the parasite and causes death.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Phytochemical screening of Celosia laxa leaves extract</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Test</th><th align="center" valign="middle" >Observation</th><th align="center" valign="middle" >Inference</th></tr></thead><tr><td align="center" valign="middle" >Simple sugar a) Molish’s test b) Fehling’s test</td><td align="center" valign="middle" >Purple colour observed at the interface Brick red precipitate formed</td><td align="center" valign="middle" >+ +</td></tr><tr><td align="center" valign="middle" >Alkaloids a) Mayer’s test b) Dragendoff’s test c) Wagner’s test</td><td align="center" valign="middle" >Cream precipitate formed Reddish brown precipitate formed Reddish brown precipitate</td><td align="center" valign="middle" >++ ++ ++</td></tr><tr><td align="center" valign="middle" >Saponin Frothing test</td><td align="center" valign="middle" >Frothing formed</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Cardiac glycosides a) Keller-killani’s test b) Salkowski’s</td><td align="center" valign="middle" >Brown ring colour is formed Reddish-brown colour at the interface formed</td><td align="center" valign="middle" >+ ++</td></tr><tr><td align="center" valign="middle" >Polyphenol Ferric chloride</td><td align="center" valign="middle" >Colour change observed</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Tanins Ferric chloride</td><td align="center" valign="middle" >Brownish green precipitate</td><td align="center" valign="middle" >+</td></tr></tbody></table></table-wrap><p>Key: + = detected; ++ = highly detected; -- = not detected</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Chemo-microscopical observation of Celosia laxa</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Test</th><th align="center" valign="middle" >Observation</th><th align="center" valign="middle" >Inferences</th></tr></thead><tr><td align="center" valign="middle" >Calcium oxalate</td><td align="center" valign="middle" >Calcium oxalate crystal was observed</td><td align="center" valign="middle" >Calcium oxalate present</td></tr><tr><td align="center" valign="middle" >Fat and oil</td><td align="center" valign="middle" >Reddish colouration was observed</td><td align="center" valign="middle" >Fat is present</td></tr><tr><td align="center" valign="middle" >Starch</td><td align="center" valign="middle" >Blue black colouration observed</td><td align="center" valign="middle" >Starch present</td></tr></tbody></table></table-wrap><p>The possible mechanism of action of tannins may be three-fold as follows: 1) interfere with energy generation by uncoupling oxidative phosphorylation; 2) they may interfere with glycoprotein of cell surface and; 3) they can bind to free proteins in the gastrointestinal tract of host animal or glycoprotein on the cuticle of the parasite and cause death [<xref ref-type="bibr" rid="scirp.113940-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.113940-ref21">21</xref>].</p><p>Alkaloids may act on central nervous system and caused paralysis of the earthworm [<xref ref-type="bibr" rid="scirp.113940-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.113940-ref22">22</xref>]. The effect would be due to presence of the steroidal alkaloid, oligoglycosides, which may suppress the transfer of sucrose from the stomach to the small intestine; hence, couple with its antioxidant effect, it is capable of reducing the nitrate generation which could interfere in local homeostasis that</p><p>is essential for the development of helminths [<xref ref-type="bibr" rid="scirp.113940-ref23">23</xref>].</p><p>Praziquantel works by causing severe spasm and paralysis of the worms’ muscles, accompanied by Ca<sup>2+</sup> influx inside the schistosome. Morphology alteration and a host of other factors are the mode of actions of the standard drug used [<xref ref-type="bibr" rid="scirp.113940-ref24">24</xref>]. Thus, the ergastic cell content recorded in the chemo-microscopy of C. laxa (<xref ref-type="table" rid="table2">Table 2</xref>), may play some role in the anthelmintic potency observed by the plant’s hydroalcoholic extracts.</p><p>Analyzing results given in <xref ref-type="table" rid="table3">Table 3</xref> and the graphs (<xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>) showed that the aqueous extract, AE at 80 mg/ml gives higher activity (no significant, p &gt; 0.05) compared to the standard Praziquantel, while at 10 - 40 mg/ml, there was significant activity in a dose dependant manner (with p &lt; 0.05) compared to the standard drug. Hence, this shows that the aqueous extract, AE, as seen in the graph (<xref ref-type="fig" rid="fig1">Figure 1</xref>), exhibited the most anthelmintic activity with the least time required to paralyzed and completely kill the earthworms at every tested concentration. Anthelmintic potency of the aqueous extract was closely followed by the methanolic extract, ME, as shown in the graph (<xref ref-type="fig" rid="fig2">Figure 2</xref>), which also exhibited significant anthelmintic activity in a dose dependent manner. However, in a conversely revealed activity pattern of AE and ME, the</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> In vitro evaluation of anthelmintic activity of C. laxa leave</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="3"  >Treatment (Extract)</th><th align="center" valign="middle"  colspan="2"  >Paralysis Time in Mins (Mean &#177; SD)</th><th align="center" valign="middle" >Death Time in Mins (Mean &#177; SD)</th></tr></thead><tr><td align="center" valign="middle"  colspan="3"  >Aqueous</td><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >10 mg/ml</td><td align="center" valign="middle"  colspan="2"  >34.5 &#177; 1.5*</td><td align="center" valign="middle" >46.0 &#177; 2.1</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >20 mg/ml</td><td align="center" valign="middle"  colspan="2"  >28.5 &#177; 2.7*</td><td align="center" valign="middle" >34.2 &#177; 4.0</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >40 mg/ml</td><td align="center" valign="middle"  colspan="2"  >24.2 &#177; 3.1a</td><td align="center" valign="middle" >30.2 &#177; 3.1</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >80 mg/ml</td><td align="center" valign="middle"  colspan="2"  >13.0 &#177; 1.8**</td><td align="center" valign="middle" >16.8 &#177; 1.5</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >Praziquantel (10 mg/ml)</td><td align="center" valign="middle"  colspan="2"  >22.0 &#177; 2.0c</td><td align="center" valign="middle" >27.0 &#177; 2.0</td></tr><tr><td align="center" valign="middle"  colspan="3"  >Methanol</td><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >10 mg/ml</td><td align="center" valign="middle"  colspan="2"  >35.0 &#177; 1.8</td><td align="center" valign="middle" >42.3 &#177; 2.3</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >20 mg/ml</td><td align="center" valign="middle" >27.8 &#177; 1.7</td><td align="center" valign="middle"  colspan="2"  >33.8 &#177; 1.2</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >40 mg/ml</td><td align="center" valign="middle" >21.7 &#177; 1.5</td><td align="center" valign="middle"  colspan="2"  >27.3 &#177; 3.4</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >80 mg/ml</td><td align="center" valign="middle" >15.7 &#177; 0.5</td><td align="center" valign="middle"  colspan="2"  >23.0 &#177; 0.0</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >Praziquantel (10 mg/ml)</td><td align="center" valign="middle" >22.0 &#177; 2.0 c</td><td align="center" valign="middle"  colspan="2"  >27.0 &#177; 2.0</td></tr><tr><td align="center" valign="middle"  colspan="3"  >Hexane</td><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  ></td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >10 mg/ml</td><td align="center" valign="middle" >10.6 &#177; 0.8</td><td align="center" valign="middle"  colspan="2"  >23.8 &#177; 1.1</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >20 mg/ml</td><td align="center" valign="middle" >13.0 &#177; 2.0</td><td align="center" valign="middle"  colspan="2"  >23.0 &#177; 2.0</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >40 mg/ml</td><td align="center" valign="middle" >35.0 &#177; 2.0</td><td align="center" valign="middle"  colspan="2"  >45.3 &#177; 0.6</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >80 mg/ml</td><td align="center" valign="middle" >22.0 &#177; 2.6</td><td align="center" valign="middle"  colspan="2"  >27.0 &#177; 1.0</td></tr><tr><td align="center" valign="middle"  colspan="2"  ></td><td align="center" valign="middle" >Praziquantel (10 mg/ml)</td><td align="center" valign="middle" >22.0 &#177; 2.0 c</td><td align="center" valign="middle"  colspan="2"  >27.0 &#177; 2.0</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>Values are expressed as mean &#177; SEM. Values were found out by using ONE way ANOVA followed by Dunnett’s t-test. ** Values are significantly different from control at (P &lt; 0.05).</p><p>hexane extract, HE, showed no significant activity, as seen from the graph (<xref ref-type="fig" rid="fig3">Figure 3</xref>). These are not far-fetched, as most research groups have estimated that greater amounts of polyphenolics are resident in polar hydroalcoholic domains.</p></sec><sec id="s6"><title>6. Conclusion</title><p>The overall findings of the present study have shown that C. laxa contains possible anthelmintic compounds due to the bioactivity records of aqueous and methanol extracts. Extract from hexane solvent had recorded no activity at the concentrations tested, indicating a likely non-synergistic mode of action by the</p><disp-formula id="scirp.113940-formula1"><graphic  xlink:href="//html.scirp.org/file/2-2311521x5.png?20211216163639976"  xlink:type="simple"/></disp-formula><p>Plate 1. Celosia laxa thriving gracefully in cultivated land habitat (Image retrieved [<xref ref-type="bibr" rid="scirp.113940-ref16">16</xref>] ).</p><p>phytoconstituents in the three extracts. Alkaloids and cardiac glycosides were detected richly in the plant and hence, not ruling out their role in the bioactivity recorded. The in vitro method used has thus, provided a means of rapidly screening the plant’s extracts for the validation of its claims as an anthelmintic and hence, indicate the plant’s potentials. Further studies, using the results of these findings as a lead, might just rightly translate to the discovery of more potent anti-infectives against parasitic (helminth) worm disease.</p></sec><sec id="s7"><title>Acknowledgments</title><p>The Lab. Technologist, Mal. Abdullahi of Pharmacology &amp; Toxicology Department, Faculty of Pharmaceutical Sciences, UDUS, was of good technical assistance to this study.</p></sec><sec id="s8"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s9"><title>Cite this paper</title><p>Mathias, S.N., Mshelia, E.H., Danbala, B.B. and Biambo, A.A. (2021) In Vitro Anthelmintic Activity of Leaf Extracts of Celosia laxa Schum. &amp; Thonn. Open Journal of Applied Sciences, 11, 1277-1286. https://doi.org/10.4236/ojapps.2021.1112097</p></sec></body><back><ref-list><title>References</title><ref id="scirp.113940-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Patel, J., Kumar, G.S., Qureshi, M.S. and Jena, P.K. (2010) Anthelmintic Activity of Ethanolic Extract of Whole Plant of Eupatorium odoratum. 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