Research

Filfil Siyāh (Piper nigrum): Medicinal importance in perspective of Unani medicine and pharmacological studies

Authors:
  • Regional research institute of Unani Medicine, Srinagar, J&K
  • Regional research institute of unani medicine srinagar
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Abstract

Piper nigrum is a perennial climbing shrub from Piperaceae family. Piper nigrum is native of the Indo-Malaysian region. Fruits of the piper (Filfil Siyāh) are used in Unani Medicine for the treatment of asthma, dyspepsia, piles, flatulence, skin diseases, respiratory diseases, toothache, fevers, and leukoderma. It is also used as carminative, liver and Gastric tonic, aphrodisiac, expectorant, emmenagogue etc. A variety of phytoconstituent are isolated from Filfil Siyāh which include alkaloids, essential oils, fats, safrol, tannic acid, amids etc. Various pharmacological studies on the plant have been done like antimicrobial, hepatoprotective, antidepressant, digestive etc. The aim of the paper is to highlight the therapeutic applications as per description in Unani literature and scientific studies done on Piper nigrum.

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In this study an attempt is made to evaluate the antimicrobial activity of various extracts of fruits of different Piper. species available in the Aurangabad-Marathwada (Maharashtra State) region. Twenty eight extracts prepared from the fruits of four species, viz. Piper cubeba Linn. f., P. retrofractum Vahl syn. P. chaba Hunter non Blume, P. longum Linn. and P. nigrum Linn. were evaluated against bacterial pathogens, such as Staphylococcus albus, Salmonella typhi, Pseudomonas aeruginosa, Escherichia coli and Bacillus megaterium and one fungus, Aspergillus niger. Compared to Streptomycin all the extracts exhibited a good antibacterial activity. Some of the extracts showed antifungal activity as well.
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The aim of this study was to investigate the effect of Piper nigrum L. root extracts on carbon tetrachloride (CCl 4)-induced rat liver injury. Among the three different extracts (water, ethanol and chloroform extract), ethanol extract exhibits the highest hepatoprotective activity (p < 0.05). When using the ethanol extract at a dose of 120 mg/ kg to treat the CCl 4 -intoxicated rat, the activities of alanine transaminase (ALT) and aspartate transanimase (AST) in rat serum decreased to 65.7 and 84.5%, respectively. At the same time, the lipid peroxidation (MDA) decreased to 52.3% and glutathione (GSH) increased to 55.8% in the rats liver homogenate, as compared with those of the CCl 4 positive control rats. The hepatoprotective effect of ethanol extract was also supported by the histopathological observations. Moreover, the ethanol extract was studied for its in vitro antioxidant activity using the methods of ferric thiocyanate (FTC) and thiobarbituric acid (TBA). The findings indicate that the ethanol extract of P. nigrum L. root is an efficient hepatoprotective and antioxidant agent against CCl 4 -induced liver injury.
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Hyperactivation of the hypothalamic-pituitary-adrenal axis and the associated hippocampal atrophy were observed in patients with depression, which could be ameliorated by the treatment with antidepressants. Therefore, neuroprotection has been proposed to be one of the acting mechanisms of antidepressant. Our previous studies have showed that treating mice with piperine produced antidepressant-like effect in animal models of behavioral despair. This study aimed to examine the protective effect of piperine treatment on corticosterone-induced neurotoxicity in cultured rat pheochromocytoma (PC12) cells. The results showed that piperine co-treatment revealed a differential effect on the cytotoxicity of corticosterone and had its maximum inhibitory effect at 1 μM. Piperine (1 μM) co-treatment also significantly decreased intracellular reactive oxygen species level, and enhanced superoxide dismutase activity and total glutathione level in corticosterone-treated PC12 cells. In addition, piperine (1 μM) co-treatment was found to reverse the decreased brain-derived neurotrophic factor (BDNF) mRNA level caused by corticosterone in PC12 cells. The results suggest that piperine exerts a neuroprotective effect on corticosterone-induced neurotoxicity in PC12 cells, at least in part, via the inhibition of oxidative stress and the upregulation of BDNF mRNA expression. This neuroprotective effect may be one of the acting mechanisms accounts for the in vivo antidepressant activity of piperine.
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