Medical Benefits Of Honey Biology Essay

Medical Benefits Of Honey Biology EssayHoney is a sticky solution which is made by worker lambbees. Nectar is a normal sweet material which is described as a whole works exudation that is gathered by making lovebees and combined with certain secretion for the mark of ripening and maturation.1 The main source of dear is f pocket-sizeer nectar which, afterwardwards collection , is modified and stored in passioncombes in order to be employ as nourishment for the young brood.2 inveterate displease handling is costly and complicated. It is estimated that 1% of the population of both the United Kingdom and United States sport a continuing ulcer, in the company of displease treatment bell in Britain only approximately about 1 billion sequester per year. The debrokerrative better is always excruciating, malodorous gate for expansionist contagious disease and a potential repository for antibiotic drug resistant bacteria.3Its difficult for patients to meet chronic lesion s for a long time and this could have effect on the patients quality of life, work prospects, relationships, and continual pain. Zumla and Lulat ( 1982 ) described that the ancient Egyptians remembered employment of edulcorate in 500 of 900 remedies. Hippocrates recognized the worth of honey as a unit of the diet, mix it with vinegar for pain, water for thirst, and water with contrary other(a) medical substances for acute fever.4 on that point ar numerous study conducted and shown made result in several fibres of wounds. Chronic wounds be casing high up incidence of hospital admission and the development of biofilms that inhabits the ameliorate in this wounds. genus Pseudomonas argonosa one of the main bacteria that dalliances in the chronic wound healing. Manuka honey has approve to be the therapeutic treatment among the ether type of honey which inhabits the development of the biofilms in give wounds.In this study, I have compargond among microtiter carapace and Cal gary base and there effectiveness pr regular(a)tive and inhibition of manuka honey. I believe that they were many patients in Oman who have diabetic chronic wound and there ar not getting good results for their cases which end them with imputative lamps. I have selected this topics because that the use of manuka honey will contri barelye enhancing the wound healing in chronic wounds.Treatment of wounds using honeyThe medical letter on medicating wounds with honey has been consulted recently in expert wound- business organization journals, with a thin on the medical indication and the clinical face. In this stage, scientists are considered on the therapeutic effectuate notice when honey is taken as a wound dressing.5There were many reports in the medical journals that show the different type of wounds has been treated successfully with honey abrasions, fistula, amputations, tail end ulcers in lepers, abscesses , infected wounds arising from arising from trauma, bed sores, large septic wounds, burns, burst abdominal wounds following cesarian delivery, level ulcers, malignant ulcers, sickle cell ulcers, skin ulcers, pottycrum, cervical ulcers, running(a) wounds, chilblains, cracked nipples, cuts, tropical ulcers ,wounds to the abdominal wall and perineum, varicose ulcers, diabetic foot ulcers and other diabetic ulcers.5Honey tail assembly founder a damp wound environment and cigaret prevent or clear existing wound infections. Its can derided wounds and remove malodour, it reduces oedema and exudates, prevents and minimises hypertrophic scarring and hastens healing. Some honeys are in stock(predicate) in the form of sterile product licensed for the use in wound fretfulness in Australia, Canada, the European Union, Hong Kong, mod Zealand ant the USA.6The type of honey which is normally used in the modern products is prepared specifically for wound management. It should be filtered, gamma irradiated and CE marked. The quantity of honey which can be used in the dressing is enough to cover the wound push through or fill the cavity or sinus, although It can crossroad the wound margins. In the UK, wound treat honey is available in liquid form, in simple dressing form ( tulle or embellish ) or in alginate dressings and the dressing may need to be changed periodical initially until the level of exudates reduces with time the period between dressing changes can be extended.PROPERTEES OF CHRONIC WOUNDSThe process of acute wound healing has been divide into four steps coagulation, inflammation, cell proliferation and repair of the matrix, and epithelialization and remodeling. The signs of an infected wound are tumor, rubor, dolor, calor, and function laesa. Other amount have been suggested, like less percutaneous oxygen tension ( TcPO2 ), presence of necrotic tissue, foul order, pan, wound submit down, or simply lack of healing.The clinical endpoint for infection has been proposed if cv bacteria/g tissue are present, the wou nd is colonized whereas higher up 105 bacteria/g tissue it is infected.The susceptibility of colonizing bacteria to generate themselves and proliferate in a biofilm due to the weak of successful antibiotic therapy. Chronic wounds divide into miscellaneous groups much(prenominal)(prenominal) as venous oarlock ulcers, diabetic foot ulcers, and pressure level ulcers. Each group has their specific principles for treatment based on current knowledge of pathogenesis. Venous outgrowth ulcers are accelerate by malfunction of venous valves causing venous hypertension in the crural veins, raised pressure in capillaries, and edema. Venous pressure more than 45mmHg inevitably leads to development of a leg ulcer. The therapy of the venous leg ulcer is compression, which often heals the ulcer. Repetitive hinderance of the neurophatic is the main cause of diabetic foot ulcer and usually ischemic foot and treatment is offloading and restitution of circulation. Pressure ulcers are produced b y sustained or repetitive load on usually vulnerable scene of actions such as the sciatic tuberculum, sacral region, heels, and shoulders in the immobilized patient. Medicament is pressure relief with discharge mattresses, cushion seats, and ambulation of the patient. Chronic wounds in the form of to be stuck in the seditious step characterized by a continuing influx of neutrophils (polymorphonuclear neutrophils PMNs) that lanch cytotoxic enzymes, free oxygen radicals, and inflammatory brokers that cause wide collateral harm to the host tissue.The two responses cellular and humoral have a part in the inflammatory methed of chronic wounds. In the infection, (polymorphonuclear neutrophils PMNs) are detected in high amounts in chronic wounds. MMPs belong to a family of zincdependent endoproteinases that are involved in the degradation of extracellular matrix (ECM) components. They are maked by several different cells, for instance fibroblasts, macrophages, eosinophils, further in pa rticular the PMNs. MMP production is stimulated by cytokines, growth factors, and cell-cell contact. The MMPs go in in the first stage of the wound-healing process, by throw devitalized tissue, and are therefore believed to play an important berth in normal wound healing and remodeling. As for the repair stage, MMPs are important for angiogenesis, wound matrix contraction, migration of fibroblasts and keratinocytes, and epithelialization. However, many papers proposed that elevated levels of active MMPs impair wound healing. Consequently, wound care items have been real that aim at relieving the supposedly disadvantage effects of elevated MMPs in order to promote healing. In especially, infections with P. aeruginosa show altered amount of MMPs and MMP-regulating cytokines. Additionally, there are rarely any reports on antibody organic evolution against P. aeruginosa, with specific reference to chronic wounds.16Pseudomonas argonosa biofilm cellsBacterial biofilms are polycellul ar communities in which cells are an integral component within an extracellular matrix at close vicinity to one another. Biofilms are after linked to consentaneous surfaces but they converse to multicellular aggregates, flocks and grauls hanging in the aqueous material body in many habitats. It may produce foul, green-pigmented discharge and necrosis.7 Also they can be assimilation by single species or mixed species consortia.They are just about figure of definite features are required for the type of biofilm organisation 1 Attachment to the involving particular agglutinant proteins.2 Cell to cell covering fire involving proteins,extra-cellular DNA and polysaccharide in order for the cells to resist the hydrodynamic furiousnesss.3 Cell motility to enable the cells to crawl on the surface.The bulk of P.aeruginosa biofilm cells even at the early stage express a type that is recollecting of gene expression seen in the early stationary phase of planktonic cells by analysis base d of transcriptomics. This would in part demonstrate the high valuation reserve to antibiotics since a lot of drugs are comparatively ineffective against slow or non-growing stationary cells. Furthermore quorum sensing ( QS ) regulated gene expression as well contributes to biofilm tolerance. Davies et al. ( 1998) explained that a QS incomplete las I mutant of P.aeruginosa formalized biofilms that were much apt(p) to biocides. Also, biofilms constituted by a las R, rhlR double mutant of P.aeruginosa is more unfastened to killing by tobramycin and hydrogen peroxide than biofilms formed by a wild-type counterpart suggestive of biofilm specific QS controlled genes.8Biofilm developmentFirst, various species shift to develop similar structural and functional endpoint over biofilm formation, including the various stage of microcolony formation, matrix embedded mature biofilms, and tolerance to antimicrobial agent. Moreover, these species may or may not employ cell surface structures such as pili, flagella and LPS.Second, the use of various channel for biofilm formation and function extend also within a species like the development of tobramycin justification in P. aeruginosa.8The biofilm life cycle. 1 each cells populate the surface. 2 extracellular polymeric substance (EPS) is produced and attachment arrests irreversible. 3 4 biofilm architecture develops and matures. 5 single cells are released from the biofil.9Manuka honeyHoney has various antimicrobial factors. slightly 80% of honey content by weight is sugar and it is relatively acidic ( typical pH ranges from 3.2 to 4.5 ), making it unsuitable for microbial growth.6Manuka honey has been promoted to therapeutic advantage over other honeys which are grown in New Zealand and Australia.10 It is reported to have a high concentration of a trimethoxybenzoic acid and methylglyoxal 2-methoxybenzoic acid and methlglyoxal were linearly related in fresh manuka honey.11 late it has been documented that the an tibacterial activity of this honey is due to reactive methylglyoxal ( MG ) which is more concentrated ( up to 100 times ) in manuka honey compared others honeys.10 This led to the development of an industry standard phenol equivalent named crotchety manuka factor ( UMF ).11 Where MG is a strong protein-glycating agent and a honest harbinger of advanced glycation end products (AGEs), GM and AGEs play a role in the pathogenesis of weakening diabetic wound healing and can compensate the structure and the function of the target molecules. Along with MG, hydrogen peroxide, flavonoid and aromatic acids are present in natural honeys.10Hydrogen peroxide is produced in low concentration by the enzyme glucose oxidase which is present in the honey from bee hypopharyageal glayls. It is produced when honey is cut with the body fluids and the acidity of the honey is neutralised also the body fluids.If the honey is used as topically like a wound dressing, hydrogen peroxide is formed by dilutio n of the honey with body fluids.C6 H12 O6 + H2O + O2 C6 H12 O7 + H2O2The New Zealand beekeeping industry recognized that storage of manuka honey increased the UMF rank and thus also its market value. The colour of honey is linked to the word form of 1,2-dicarbonyl compounds output on non-enzymatic caramelisation or Maillard reactions see Figure 2.11Figure 2. master(prenominal) properties of manuka honey in the treatment of diabetic ulcers. The black arrow represents know action, the white arrows represent hypothetical mechanisms of action. MG methylglyoxal AGEs advanced glycation end products MRJP1 major(ip) royal jelly protein.3In addition, ripeness of stored honeys has been showed to increase the 5-hydroxymethylfurfural ( HMF ) amount. Another thing is that some beekeeper in New Zealand are heating the honey to ascertain the UMF activity which may raise HMF beyond the current international standard of 40mg/kg for culinary honeys.11The susceptibility of the honey to effect the action of the cells that are central to the wound healing method has been investigated by exposing monocytic cells to diluted honey and measuring the rate of release of cytokines that indicate cell activitation. Monocytes are precursors of macrophages, which are substantial cellular organizers of wound healing. Impaired healing is formed by numerous, complex factors which are not entirely understood at present, but it has been linked to reduced numbers of macroghages and inactive macrophages. The susceptibility of agents to stimulation such cells therefore has importance in estimate their wound healing potential.12There were a study published for comparison of desloughing efficacy after 4 hebdomads and healing outcomes after 12 weeks in sloughy venous leg ulcers treated with Manuka honey ( hurtcare 18+ ) vs. Standard hydrogel therapy ( Intrasite change ). The study shows 108 patients with venous leg ulcers having 50 wound area covered in slough, not taking antibiotic or immunosup pressant therapy were recruited from ascular centres, acute and community care hospitals and leg ulcer clinics. The efficacy of wound care 18+ to deslough the wounds after 4 weeks and its impact on healing after 12 weeks when campared with IntraSite Gel control was determined. The treatment was applied weekly for 4 weeks and follow up was made at week 12.From the results of the study it was demonstrated that at week 4, mean percentage of reduction in slough was 67% Wound Care 18+ vs. 52.9% Intra Site Gel (p = 0.054). Mean wound area covered in slough reduced to 29% and 43%, separately (p = 0.065). Median reduction in wound size was 34% vs. 13% (p = 0.001). At 12 weeks, 44% vs. 33% healed (p = 0.037). Wounds having 50% reduction in slough had greater probability of healing at week 12 (95% confidence interval 1.12, 9.7 risk ratio 3.3 p = 0.029). Infection developed in 6 of the WoundCare18+ group vs. 12 in the IntraSite Gel group.The WoundCare 18+ group had increased incidence of heal ing, effective desloughing and a lower incidence of infection than the control. Manuka honey has therapeutic value. This study confirmd that manuka honey may be considered by clinicians for use in sloughy venous ulcers.13Calgary Biofilm PlatesThe Calgary Biofim Plates was developed at the University of Calgary by their microbiologists. This Device now has a commercial name as The MBEC assay. It working by the idea of the microorganisms to grow on 96 pegs stick out down from a plastic lid. The MBEC assay plate has two parts. The hurrying part of the plate is polystyrene lid with 96 identical pegs. The mean surface area of each peg is 108.9mm2. The lid is inserted into the lower part of the plate a microtiter plate is set up to contain an inoculated growth medium. The plate is kept on a gyrorotary shaker in an incubator, which provides the shearing force that facilitates the formation of 96 biofilms on the peg lid. Biofilms take shape on the polystyrene pegs when planktonic bacteria adsorb to the surface. In the presence of shear, these bacteria become irreversibly attached and grow to form mature biofilms.14