Relative Free Radical Scavenging, Tyrosinase Inhibitory, and Anti-Inflammatory Potential of the Polar Peel decoctures of distinct Malus Species indigenous to Kashmir

Amit Gupta, Ashfaq Ahmad Shah, Akshita Rawat, Tanvi Parihar, Yashaswi Singh, Neha Pandey, Vijay Kumar
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Abstract

Apple, (Malus domestica, Brokh), is a vital source of phenolic and polyphenolic compounds whose accumulation in the different parts of the fruit depends upon various intrinsic and extrinsic factors. This study aimed to perform a comparative evaluation of phenolics of peels of three red-skinned (“Delicious”, “Maharaji”, “Royal delicious”), and one yellow-skinned (“Golden Delicious”) apple varieties incorporating preliminary secondary metabolite perusal followed by estimation of Total phenol and total flavonoid contents. Secondary phytocompounds being usually polar in nature were extracted from peels via the Soxhlet and hot maceration processes using different menstruum systems of varied polarity. Comparative assessment of Free radical scavenging, anti-pigmentation, and anti-inflammatory properties of all the decoctures was analyzed thereafter.Free radical scavenging capacity was analyzed via 2, 2-diphenyl-1-picrylhydrazyl assay.Tyrosinase inhibitory activity was assessed by studying the in vitro impact of decoctures on the monophenolase and diphenolase reactions of the enzyme tyrosinase. The anti-inflammatory potential of the samples was assessed by inhibition of hypotonicity-induced HRBC membrane lysis. TPC/TFC estimation was analyzed via spectrophotometry. Methanol crude peel extracts of all apple species revealed rich phytochemical content as per TPC/TFC analysis. In a dose-dependent manner, all the crude peel extracts demonstrated considerable free radical scavenging capacity with DPPH assay. Maharaji methanolic decocture revealed potent free radical scavenging activity by showing the lowest IC50 value while Royal delicious acetone extract showed the highest IC50 value when collated with the potent reference antioxidant ascorbic acid with an IC50value of 114.62µg/ml. Polarextract of Malus domestica var Maharaji revealed significant tyrosinase inhibitory activity by revealing IC50 of 8460.65µg/mlon L-Tyrosine substrate and IC50 of 7830.46 µg/ml on L-DOPA substrate. Malus peel compounds turn out to be more effective in diphenolase reaction and kojic acid acts more effectively in the monophenolase one.At various concentrations, the percentage of membrane stabilization for methanolic extracts and the reference NSAID diclofenac sodium was determined.The highest level of membrane stabilization wasshown by methanolic Maharaji and delicious apple peel extracts (83.76 % and 72.32% at a dose of 200 mg/ml respectively) when juxtaposed with standard NSAID showing 98.58 % inhibition at a concentration of 25 mg/ml. Methanol extracts of Malus domestica var Maharaji out performed the other Malus peel extracts in terms of all the parameters analyzed, according to the current study. So, this study is giving the highest pharmaceutical priority to the Malus domestica var Maharaji when it comes to human-health benign bioactive compounds, oxidative stress-related diseases, pigmentation disorders, and inflammatory diseases.
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克什米尔不同苹果品种极性果皮煎剂的相对自由基清除、酪氨酸酶抑制和抗炎潜力
苹果(Malus domestica, Brokh)是酚类和多酚类化合物的重要来源,其在果实不同部位的积累取决于各种内在和外在因素。本研究旨在通过初步的次级代谢物分析,对三种红皮苹果(“Delicious”、“Maharaji”、“Royal Delicious”)和一种黄皮苹果(“Golden Delicious”)果皮中的酚类物质进行比较评价,并对总酚和总黄酮含量进行估算。从果皮中提取极性次生植物化合物,采用索氏浸渍法和热浸渍法,采用不同极性的基质体系。比较评价各煎剂的自由基清除、抗色素沉着和抗炎作用。通过2,2 -二苯基-1-苦味酰肼法测定自由基清除能力。通过研究煎剂对酪氨酸酶单酚酶和二酚酶反应的体外影响,评价其酪氨酸酶抑制活性。通过抑制低渗诱导的HRBC膜溶解来评估样品的抗炎潜力。用分光光度法测定TPC/TFC。TPC/TFC分析表明,所有苹果品种的甲醇粗皮提取物均含有丰富的植物化学成分。在剂量依赖的方式,所有粗皮提取物显示相当大的自由基清除能力与DPPH测定。Maharaji甲醇煎液的IC50值最低,而Royal delicious丙酮煎液与抗坏血酸对照的IC50值最高,为114.62µg/ml。对L-DOPA底物的IC50为7830.46µg/ml,对l -酪氨酸底物的IC50为8460.65µg/ml。果皮化合物在二酚酶反应中更有效,而曲酸在单酚酶反应中更有效。在不同浓度下,测定了甲醇提取物和对照非甾体抗炎药双氯芬酸钠的膜稳定率。与浓度为25 mg/ml的标准非甾体抗炎药相比,甲醇Maharaji和美味苹果皮提取物的膜稳定性最高,分别为200 mg/ml时的83.76%和72.32%。根据目前的研究,国产苹果皮甲醇提取物在所有参数分析方面都优于其他苹果皮提取物。因此,当涉及到人类健康的良性生物活性化合物,氧化应激相关疾病,色素沉着障碍和炎症性疾病时,本研究将最高的药物优先权给予了家苹果var Maharaji。
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