Mubin Sidra, Rehman Najeeb Ur, Murad Waheed, Shah Muddaser, Al-Harrasi Ahmed, Afza Rabia
Department of Botany, Hazara University Mansehra, Mansehra 21310, Pakistan.
Natural and Medical Sciences Research Center, University of Nizwa, Birkat Al Mauz, Nizwa 616, Oman.
Antioxidants (Basel). 2022 Jul 26;11(8):1446. doi: 10.3390/antiox11081446.
The recent investigation was designed to explore Hemsl. ex Lace & Prain (Lamiaceae) whole plant in various extracts (methanol (SPM), dichloromethane (SPDCM), n-Hexane (SPNH), and aqueous (SPAQ) for a phytochemicals assessment, ESI-LC-MS chemical analysis, in vitro antimicrobials, and antioxidants and in vivo anti-inflammatory and analgesic potential. The qualitative detection shows that all the representative groups were present in the analyzed samples. The examined samples display the greatest amount of total flavonoid content (TFC, 78.2 ± 0.22 mg QE/mg) and total phenolic contents (TPC, 66.2 ± 0.33 mg GAE/g) in the SPM extract. The SPM extract proceeded to the ESI-LC-MS to identify the chemical constituents that presented nineteen bioactive ingredients, depicted for the first time from mainly contributed by flavonoids. The analyzed samples produced considerable capability to defy the microbes. The SPM extract was observed effective and offered an appreciable zone of inhibition (ZOI), 17.8 ± 0.04 mm against the bacterial strain and 18.8 ± 0.04 mm against . Moreover, the SPM extract also exhibited 19.4 ± 0.01 mm against the bacterial strains and 18.8 ± 0.04 mm against in comparison to the standard levofloxacin (Gram-negative) and erythromycin (Gram-positive) bacterial strains that displayed 23.6 ± 0.02 mm and 23.2 ± 0.05 mm ZOI, correspondingly. In addition to that, the SPD fraction was noticed efficiently against the fungal strains used with ZOI 19.07 ± 0.02 mm against and 18.87 ± 0.04 mm against the as equated to the standard with 21.5 ± 0.02 mm ZOI. In the DPPH (2,2-diphenyl-1-picrylhydrazyl) analysis, the SPM extract had the maximum scavenging capacity with IC of 78.75 ± 0.19 µg/mL succeeded by the SPDCM fraction with an IC of 140.50 ± 0.20 µg/mL free radicals scavenging potential. Through the ABTS (2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) assay, the similar extract (SPM) presented an IC = 85.91 ± 0.24 µg/mL followed by the SPDCM fractions with IC = 182.50 ± 0.35 µg/mL, and n-Hexane fractions were reported to be the least active between the tested samples in comparison to ascorbic acid of IC = 67.14 ± 0.25 µg/mL for DPPH and IC of 69.96 ± 0.18 µg/mL for ABTS assay. In the in vivo activities, the SPM extract was the most effective with 55.14% inhibition as compared to diclofenac sodium with 70.58% inhibition against animals. The same SPM crude extract with 50.88% inhibition had the most analgesic efficacy as compared to aspirin having 62.19% inhibition. Hence, it was assumed from our results that all the tested samples, especially the SPM and SPDCM extracts, have significant capabilities for the investigated activities that could be due to the presence of the bioactive compounds. Further research is needed to isolate the responsible chemical constituents to produce innovative medications.
最近的一项研究旨在探索糙苏(唇形科)全草的各种提取物(甲醇提取物(SPM)、二氯甲烷提取物(SPDCM)、正己烷提取物(SPNH)和水提取物(SPAQ)),以进行植物化学评估、电喷雾电离液相色谱-质谱联用(ESI-LC-MS)化学分析、体外抗菌和抗氧化以及体内抗炎和镇痛潜力研究。定性检测表明,所有代表性成分均存在于分析样品中。在所检测的样品中,SPM提取物的总黄酮含量(TFC,78.2±0.22毫克槲皮素当量/毫克)和总酚含量(TPC,66.2±0.33毫克没食子酸当量/克)最高。SPM提取物进行了ESI-LC-MS分析以鉴定化学成分,结果显示有19种生物活性成分,这是首次从该植物中鉴定出来,主要成分是黄酮类化合物。分析样品对微生物具有相当强的抵抗能力。观察到SPM提取物有效,对细菌菌株的抑菌圈(ZOI)为17.8±0.04毫米,对[具体细菌菌株2]的抑菌圈为18.8±0.04毫米。此外,与标准左氧氟沙星(革兰氏阴性菌)和红霉素(革兰氏阳性菌)相比,SPM提取物对[具体细菌菌株3]的抑菌圈为19.4±0.01毫米,对[具体细菌菌株4]的抑菌圈为18.8±0.04毫米,标准左氧氟沙星和红霉素的抑菌圈分别为23.6±0.02毫米和23.2±0.05毫米。除此之外,与标准品抑菌圈为21.5±0.02毫米相比,SPD部分对所用真菌菌株有效,对[具体真菌菌株1]的抑菌圈为19.07±0.02毫米,对[具体真菌菌株2]的抑菌圈为18.87±0.04毫米。在二苯基苦味酰基自由基(DPPH)分析中,SPM提取物的清除能力最强,半数抑制浓度(IC)为78.75±0.19微克/毫升,其次是SPDCM部分,IC为140.50±0.20微克/毫升,具有自由基清除潜力。通过2,2'-联氮-双-3-乙基苯并噻唑啉-6-磺酸(ABTS)测定法,类似提取物(SPM)的IC = 85.91±0.24微克/毫升,其次是SPDCM部分,IC = 182.50±0.3微克/毫升,与抗坏血酸相比,在所测试的样品中,正己烷部分的活性最低,抗坏血酸在DPPH测定中的IC = 67.14±0.25微克/毫升,在ABTS测定中的IC = 69.96±0.18微克/毫升。在体内活性方面,与双氯芬酸钠对动物的抑制率70.58%相比,SPM提取物最有效,抑制率为55.14%。与阿司匹林抑制率62.19%相比,相同的SPM粗提取物抑制率为50.88%,具有最强的镇痛效果。因此,从我们的结果可以推测,所有测试样品,尤其是SPM和SPDCM提取物,对于所研究的活性具有显著能力,这可能归因于生物活性化合物的存在。需要进一步研究分离出起作用的化学成分以生产创新药物。