| Literature DB >> 36235480 |
Hatun A Alomar1, Noha Fathallah2, Marwa M Abdel-Aziz3, Taghreed A Ibrahim4,5, Wafaa M Elkady2.
Abstract
Eradication of Helicobacter pylori is a challenge due to rising antibiotic resistance and GIT-related disorders. Cuminum cyminum, Pimpinella anisum, and Carum carvi are fruits belonging to the Apiaceae family. Their essential oils were extracted, analyzed using GC-MS, tested for anti-H. pylori activity by a micro-well dilution technique, identified for potential anti-H. pylori inhibitors by an in-silico study, and investigated for anti-inflammatory activity using a COX-2 inhibition assay. Results showed that the main components of C. cyminum, P. anisum, and C. carvi were cumaldehyde (41.26%), anethole (92.41%), and carvone (51.38%), respectively. Essential oil of C. cyminum exhibited the greatest anti-H. pylori activity (3.9 µg/mL) followed by P. anisum (15.63 µg/mL), while C. carvi showed the lowest activity (62.5 µg/mL). The in-silico study showed that cumaldehyde in C. cyminum has the best fitting energy to inhibit H. pylori.C. cyminum essential oil showed the maximum ability to reduce the production of Cox-2 expression approaching celecoxib with IC50 = 1.8 ± 0.41 µg/mL, followed by the C. carvi oil IC50 = 7.3 ± 0.35 µg/mL and then oil of P. anisum IC50 = 10.7±0.63 µg/mL. The investigated phytochemicals in this study can be used as potential adjunct therapies with conventional antibiotics against H. pylori.Entities:
Keywords: Carum carvi; Cuminum cyminum; GC-MS Helicobacter pylori; Pimpinella anisum; anti-inflammatory; antibacterial; essential oil; molecular docking
Year: 2022 PMID: 36235480 PMCID: PMC9570728 DOI: 10.3390/plants11192617
Source DB: PubMed Journal: Plants (Basel) ISSN: 2223-7747
Chemical compositions of the isolated essential oils.
| Compound | RI exp | RI rep |
|
|
| References |
|---|---|---|---|---|---|---|
| 1- Monoterpenoids | ||||||
| Cumin aldehyde | 1283 | 1283 | 41.26 | n.d | n.d | [ |
| Limonene | 1027 | 1027 | 0.77 | 1.57 | 48.49 | [ |
| Carvone | 1244 | 1249 | n.d | n.d | 51.38 | [ |
| Anethole | 918 | 918 | n.d | 92.41 | n.d | [ |
| ɣ-Terpinene | 1049 | 1049 | 8.11 | n.d | n.d | [ |
| 1,4- | 1784 | 1784 | 12.84 | n.d | n.d | [ |
| Myrtenal | 1237 | 1237 | 19.26 | n.d | n.d | [ |
| α-Pinene | 933 | 930 | 0.43 | n.d | n.d | [ |
| β-Pinene | 969 | 973 | 10.27 | n.d | n.d | [ |
| β-Myrcene | 980 | 985 | 0.41 | n.d | 0.13 | [ |
| 1441 | 1441 | 5.22 | n.d | n.d | [ | |
| Estragole | 1197 | 1197 | n.d | 3.01 | n.d | |
| 1034 | 1034 | n.d | 0.22 | n.d | [ | |
| 1130 | 1129 | 1.26 | n.d | n.d | [ | |
| 2- Sesquiterpenoids | ||||||
| β-Chamigrene | 1478 | 1478 | n.d | 0.20 | n.d | [ |
| Zingiberene | 1494 | 1494 | n.d | 0.26 | n.d | [ |
| β-Himachalene | 1505 | 1505 | n.d | 0.10 | n.d | [ |
| Longifolene | 1532 | 1532 | n.d | 2.11 | n.d | [ |
| % of identification | 99.83 | 97.21 | 100 | |||
All compounds were identified by Kováts index and mass spectral data by comparing values reported in the literature. RI Kovats index was determined experimentally relative to C8–C28 n-alkanes. RI reported Kovats retention indices.
Figure 1GC chromatograms of the essential oils of (A) C. cyminum, (B) P. anisum, and (C) C. carvi.
Figure 22D structures of the main detected compounds of three oils L. by GC–MS analysis (Drawn by Chem-draw ultra-version 14).
Mean of H. pylori inhibitory % of three extracted essential oils against the standard drug clarithromycin.
| Sample conc. (µg/mL) | Mean of | |||
|---|---|---|---|---|
| Clarithromycin * |
|
|
| |
| 125 | 100 | 100.00 | 100.00 | 100.00 |
| 62.5 | 100 | 100.00 | 100.00 | 100.00 |
| 31.25 | 100 | 100.00 | 100.00 | 81.63 ± 1.3 |
| 15.63 | 100 | 100.00 | 100.00 | 70.64 ± 2.1 |
| 7.81 | 100 | 100.00 | 79.21 ± 0.5 | 46.21 ± 0.59 |
| 3.9 | 100 | 100.00 | 51.74 ± 1.3 | 21.74 ± 1.3 |
| 1.95 | 100 | 81.97 ± 0.95 | 29.39 ± 0.6 | 8.29 ± 0.74 |
| 0.98 | 92.45 ± 1.2 | 73.25 ± 1.3 | 17.92 ± 1.5 | 3.71 ± 0.91 |
| 0.48 | 87.65 ± 0.5 | 59.31 ± 1.6 | 6.34 ± 0.74 | 0.00 |
| 0.24 | 81.35 ± 1.5 | 27.28 ± 1.0 | 0.00 | 0.00 |
| 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| MIC | 1.95 | 3.9 | 15.63 | 62.5 |
* All determinations were carried out in a triplicate manner and values are expressed as the mean ± SD.
Figure 3Anti-inflammatory activity cyclooxygenase COX-2 inhibitory % of CM (C. cyminum), AN (P. anisum), and CR (C. carvi) compared to standard drug, celecoxib.
Free binding energies (∆G) of the identified compounds within the 3NM4 active site calculated in kcal/mol using Discovery Studio 4.5, adopting both rule-based ionization techniques.
| Compound | Binding Energy ∆G (Kcal/mol) |
|---|---|
| Cumaldehyde | −28.75 |
| Estragole | −28.72 |
| −28.49 | |
| TRIS | −28.24 |
| (-)-Carvone | −28.22 |
| Anethole | −28.01 |
| ɣ-terpinene | −25.32 |
| Limonene | −25.26 |
| α Thujenal | −22.32 |
| β Pinene | −21.88 |
| Myrtenal | −20.80 |
Figure 42D and 3D interaction diagram of the co-crystallized ligand and identified compounds docking pose interactions with the key amino acids in the 3NM4 binding site. The three-letter amino acid codes and positions of each residue are indicated. Between the receptor and the ligand, hydrogen-bonding interactions are illustrated by a green dashed line, whereas -alkyl interactions are represented by a purple dashed line.