| Literature DB >> 33158437 |
Pawi Bawitlung Lalthanpuii1, Kholhring Lalchhandama2.
Abstract
BACKGROUND: Imperata cylindrica is considered as an agricultural weed, but it is a valuable plant in the traditional medicines of Southeast Asia. In the Mizo traditional medicine of India and Myanmar, the rhizomes and roots are used as a remedy for bacterial, fungal and intestinal helminth infections.Entities:
Keywords: Anthelmintic; Medicinal plant; Roundworm; Scanning electron microscopy; Tapeworm
Mesh:
Substances:
Year: 2020 PMID: 33158437 PMCID: PMC7648271 DOI: 10.1186/s12906-020-03125-w
Source DB: PubMed Journal: BMC Complement Med Ther ISSN: 2662-7671
Fig. 1GC-MS chromatogram of the chloroform extract of I. cylindrica underground parts. Total retention time was 55 min
List of compounds identified from chloroform extract of I. cylindrica underground parts using GC-MS
| Sl. no | Retention time (min) | Compound | Formula | Molecular weight (Da) | Abundance (%) |
|---|---|---|---|---|---|
| 1. | 10.38 | 3,5-Bis (1,1-dimethylethyl)-4-hydroxy benzenepropanoic acid, octadecyl ester | C36H62O3 | 530 | 1.1 |
| 2. | 15.31 | 13-Heptadecyn-1-ol | C17H32O | 252 | 1.1 |
| 3. | 18.42 | 6-Methylenebicyclo [3.2.0] hept-3-en-2-one | C8H8O | 120 | 1.0 |
| 4. | 23.14 | 2-Methoxy-4-vinylphenol | C9H10O2 | 150 | 1.0 |
| 5. | 23.55 | 3-(Chloroacetoxy)-4-methoxy benzaldehyde | C10H9CIO2 | 228 | 1.9 |
| 6. | 25.80 | 2-Octyl cyclopropanetetradecanoic acid, methyl ester | C26H50O2 | 394 | 1.2 |
| 7. | 26.63 | 2,4-Di-tert-butylphenol | C14H22O | 206 | 11.0 |
| 8. | 28.49 | 9-Hexadecen-1-ol | C16H32O | 240 | 9.7 |
| 9. | 28.68 | 2,2,4-Trimethyl-1,3-pentanediol diisobutyrate | C16H30O4 | 286 | 4.2 |
| 10. | 32.22 | (E)-4-(3-Hydroxyprop-1-en-1-yl)-2-methoxyphenol | C10H12O3 | 180 | 1.2 |
| 11. | 32.93 | Palmitic acid, methyl ester | C17H34O2 | 270 | 9.5 |
| 12. | 36.55 | Palmitic acid (hexadecanoic acid) | C16H32O2 | 256 | 15.5 |
| 13. | 36.94 | L-Methionyl-D-glutaminyl-D-methionyl-L-asparaginyl-L-lysyl-L-valyl-L-leucyl-D-α-aspartyl-L-serine | C43H76N12O15S21 | 1064 | 7.0 |
| 14. | 38.24 | Methyl 9-cis, 11 trans-octadecadienoate | C19H34O2 | 294 | 2.5 |
| 15. | 39.69 | (Z)-18-Octadec-9-enolide | C18H32O2 | 280 | 11.8 |
| 16. | 40.17 | Octadecanoic acid | C18H36O2 | 284 | 10.9 |
| 17. | 40.60 | Heptacos-1-ene | C27H54 | 378 | 3.6 |
| 18. | 43.48 | Octadecanoic acid, ethyl ester | C25H42O2 | 374 | 1.7 |
| 19. | 46.46 | Diisooctyl phthalate | C24H38O4 | 390 | 7.7 |
| 20. | 49.38 | 17α,21β-28,30-Bisnorhopane | C28H48 | 384 | 1.5 |
| 21. | 50.80 | Campesterol | C28H48O | 400 | 1.4 |
| 22. | 51.56 | Stigmasterol | C29H48O | 412 | 1.4 |
Anthelmintic activity of the chloroform extract of I. cylindrica on R. tetragona
| Treatment | Dose (mg/ml) | Normalised survival time (hour) in mean ± SD | ||
|---|---|---|---|---|
| Control | 0 | 100.00 ± 2.00 | NA | NA |
| Albendazole | 1.25 | 024.07 ± 1.62* | 114.35 | 2.05 |
| 2.5 | 020.51 ± 1.21* | 131.56 | 2.07 | |
| 5 | 016.56 ± 0.99* | 144.85 | 2.08 | |
| 10 | 012.22 ± 1.05* | 150.56 | 2.08 | |
| 20 | 004.70 ± 0.84* | 170.05 | 2.09 | |
| 1.25 | 091.81 ± 2.36* | 010.25 | 2.05 | |
| 2.5 | 089.40 ± 1.71* | 015.60 | 2.05 | |
| 5 | 082.48 ± 3.02* | 018.74 | 2.06 | |
| 10 | 064.73 ± 2.55* | 042.15 | 2.06 | |
| 20 | 036.53 ± 2.67* | 073.85 | 2.06 |
NA Not applicable; n = 15; t value is the calculated difference represented in units of standard error, the higher the value, the greater the evidence against the null hypothesis; t critical value denotes the value that must be exceeded to get a significant level
*Significantly different at p < 0.05 against control
Anthelmintic activity of the chloroform extract of I. cylindrica on A. galli
| Treatment | Dose (mg/ml) | Normalised survival time (hour) in mean ± SD | ||
|---|---|---|---|---|
| Control | 0 | 100.00 ± 0.97 | NA | NA |
| Albendazole | 1.25 | 043.54 ± 0.97* | 159.16 | 2.05 |
| 2.5 | 036.74 ± 0.83* | 192.16 | 2.05 | |
| 5 | 026.15 ± 0.72* | 236.69 | 2.06 | |
| 10 | 008.12 ± 0.92* | 266.53 | 2.05 | |
| 20 | 001.81 ± 0.38* | 365.24 | 2.10 | |
| 1.25 | 095.67 ± 1.77* | 008.30 | 2.07 | |
| 2.5 | 090.13 ± 1.63* | 020.13 | 2.07 | |
| 5 | 084.46 ± 1.10* | 040.99 | 2.05 | |
| 10 | 082.94 ± 2.11* | 028.42 | 2.09 | |
| 20 | 081.56 ± 1.71* | 036.43 | 2.07 |
NA Not applicable; n = 15; t value is the calculated difference represented in units of standard error, the higher the value, the greater the evidence against the null hypothesis; t critical value denotes the value that must be exceeded to get a significant level
*Significantly different at p < 0.05 against control
Fig. 2Scanning electron micrographs of an untreated R. tetragona. a The anterior end showing a bulbuous terminal called the scolex which bears prominent suckers (arrows). × 370. Scale bar = 50 μm. b A single sucker which is oval shaped and lined with several rows of hooks (arrows). × 1000. Scale bar = 10 μm. c The body segments called proglottids with smooth tegument due to fine microscopic hairs, the microtriches. × 750. Scale bar = 20 μm
Fig. 3Scanning electron micrographs of R. tetragona treated with I. cylindrica extract. a The scolex indicating damage of tegumental (upper arrow) and suckers (lower arrow). × 400. Scale bar = 50 μm. b A sucker indicates clumping (upper arrow) and erosion at the central pit (lower arrow). × 1000. Scale bar = 10 μm. c The proglottids are wrinkled (upper arrow) and the tegument appears fuzzy due to degeneration of microtriches (lower arrow). × 1100. Scale bar = 10 μm
Fig. 4Scanning electron micrographs of an untreated A. galli. a The anterior part bears three terminal blob-like structures called the lips, which have small protrusion called papilla (upper arrow) and surround the mouth (lower arrow). × 400. Scale bar = 50 μm. b The body surface called the cuticle in the middle of the body is smooth and lined with parallel rows of transverse striations called annulations (arrows). × 500. Scale bar = 50 μm. c The posterior end is the tail which bears anal opening or cloaca (top arrow), a precloacal sucker (middle arrow) and sensory protrusions called phasmids (bottom arrow). × 80. Scale bar = 200 μm
Fig. 5Scanning electron micrographs of A. galli treated with I. cylindrica extract. a The lips are shrunk and contracted (upper arrow) and the surrounding cuticle is also shrivelled (lower arrow). × 350. Scale bar = 50 μm. b Extensive shrinkage of the main body with formation of warts on the cuticle (arrows). × 550. Scale bar = 20 μm. c Shrinkage extends to the tail (top arrow), phasmids are distorted (middle arrow) and there is scar formation in the precloacal sucker (bottom arrow). × 110. Scale bar = 100 μm