Limon Otu

Bitki adı: Lemon Grass, herb
Bilimsel adı: Cymbopogon citratus
Diğer adları: Lemon Grass

LİMON OTU — > Oğul otu.[Türkçe Bitki Adları Sözlüğü, Turhan Baytop, 2007]


Cymbopogon citratus

Genel Bilgiler


Duke – Ethnobotany

Bilgi: Duke USEAGE: G | Leung
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Leung
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb28: 5
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Leung
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Leung
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Gupta
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Leung
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb22: 97
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Standley,Steyermark
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb22: 97
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Pittier
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Gupta
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Standley,1931
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Gupta
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Pittier
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Gupta
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb28: 5
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Gupta
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb28: 5
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb22: 97
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Standley,Steyermark
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb28: 5
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Gupta
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Liogier
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Liogier
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb22: 97
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Leung
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Burkill,1966
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Liogier
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Pittier
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | L
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb22: 97
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Woi.2
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Steinmetz
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Pittier
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Eb30: 109
Kaynak: James A. Duke
Bilgi: Duke USEAGE: G | Wong
Kaynak: James A. Duke

Bilimsel Araştırmalar

Acetaminophen (APAP) overdose is the leading cause of drug-induced acute liver failure in many developed countries. Mitochondrial oxidative stress is considered to be the predominant cellular event in APAP-induced liver injury. Accordingly, N-acetyl cysteine, a known scavenger of reactive oxygen species (ROS), is recommended as an effective clinical antidote against APAP-induced acute liver injury (AILI) when it is given at an early phase; however, the narrow therapeutic window limits its use. Hence, the development of novel therapeutic approaches that can offer broadly protective effects against AILI is clearly needed. To this end, it is necessary to better understand the mechanisms of APAP hepatotoxicity. Up to now, in addition to mitochondrial oxidative stress, many other cellular processes, including phase I/phase II metabolism, endoplasmic reticulum stress, autophagy, sterile inflammation, microcirculatory dysfunction, and liver regeneration, have been identified to be involved in the pathogenesis of AILI, providing new targets for developing more effective therapeutic interventions against APAP-induced liver injury. In this review, we summarize intracellular and extracellular events involved in APAP hepatotoxicity, along with emphatic discussions on the possible therapeutic approaches targeting these different cellular events.

Makaleyi görüntüle
Agonists of the nuclear receptor PPARγ are therapeutically used to combat hyperglycaemia associated with the metabolic syndrome and type 2 diabetes. In spite of being effective in normalization of blood glucose levels, the currently used PPARγ agonists from the thiazolidinedione type have serious side effects, making the discovery of novel ligands highly relevant. Natural products have proven historically to be a promising pool of structures for drug discovery, and a significant research effort has recently been undertaken to explore the PPARγ-activating potential of a wide range of natural products originating from traditionally used medicinal plants or dietary sources. The majority of identified compounds are selective PPARγ modulators (SPPARMs), transactivating the expression of PPARγ-dependent reporter genes as partial agonists. Those natural PPARγ ligands have different binding modes to the receptor in comparison to the full thiazolidinedione agonists, and on some occasions activate in addition PPARα (e.g. genistein, biochanin A, sargaquinoic acid, sargahydroquinoic acid, resveratrol, amorphastilbol) or the PPARγ-dimer partner retinoid X receptor (RXR; e.g. the neolignans magnolol and honokiol). A number of in vivo studies suggest that some of the natural product activators of PPARγ (e.g. honokiol, amorfrutin 1, amorfrutin B, amorphastilbol) improve metabolic parameters in diabetic animal models, partly with reduced side effects in comparison to full thiazolidinedione agonists. The bioactivity pattern as well as the dietary use of several of the identified active compounds and plant extracts warrants future research regarding their therapeutic potential and the possibility to modulate PPARγ activation by dietary interventions or food supplements.

Makaleyi görüntüle
Essential oils (EOs) have been long recognized for their antibacterial, antifungal, antiviral, insecticidal and antioxidant properties. They are widely used in medicine and the food industry for these purposes. The increased interest in alternative natural substances is driving the research community to find new uses and applications of these substances. EOs and their components show promising activities against many food-borne pathogens and spoilage microorganisms when tested in vitro. In food systems, higher concentrations of EOs are needed to exert similar antibacterial effects as those obtained in in vitro assays. The use of combinations of EOs and their isolated components are thus new approaches to increase the efficacy of EOs in foods, taking advantage of their synergistic and additive effects. The purpose of this review is to provide an overview on the antimicrobial efficacy of these combinations. A survey of the methods used for the determination of the interactions and mechanisms involved in the antimicrobial activities of these combinations are also reported.

Makaleyi görüntüle
Essential oils are aromatic and volatile liquids extracted from plants. The chemicals in essential oils are secondary metabolites, which play an important role in plant defense as they often possess antimicrobial properties. The interest in essential oils and their application in food preservation has been amplified in recent years by an increasingly negative consumer perception of synthetic preservatives. Furthermore, food-borne diseases are a growing public health problem worldwide, calling for more effective preservation strategies. The antibacterial properties of essential oils and their constituents have been documented extensively. Pioneering work has also elucidated the mode of action of a few essential oil constituents, but detailed knowledge about most of the compounds' mode of action is still lacking. This knowledge is particularly important to predict their effect on different microorganisms, how they interact with food matrix components, and how they work in combination with other antimicrobial compounds. The main obstacle for using essential oil constituents as food preservatives is that they are most often not potent enough as single components, and they cause negative organoleptic effects when added in sufficient amounts to provide an antimicrobial effect. Exploiting synergies between several compounds has been suggested as a solution to this problem. However, little is known about which interactions lead to synergistic, additive, or antagonistic effects. Such knowledge could contribute to design of new and more potent antimicrobial blends, and to understand the interplay between the constituents of crude essential oils. The purpose of this review is to provide an overview of current knowledge about the antibacterial properties and antibacterial mode of action of essential oils and their constituents, and to identify research avenues that can facilitate implementation of essential oils as natural preservatives in foods.

Makaleyi görüntüle
Essential oils are complex mixtures isolated from aromatic plants which may possess antioxidant and anti-inflammatory activities of interest in thye food and cosmetic industries as well as in the human health field. In this work, a review was done on the most recent publications concerning their antioxidant and anti-inflammatory activities. At the same time a survey of the methods generally used for the evaluation of antioxidant activity and some of the mechanisms involved in the anti-inflammatory activities of essential oils are also reported.

Makaleyi görüntüle

Kaynaklar ve Görseller

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