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Biochemical investigation of anti-cancer activity of Tulbaghia violaceaSaibu, Gbemisola Morounke January 2012 (has links)
Natural products have been a source of many pharmaceutical drugs and a number of drugs that are currently used in the treatment of cancer are derivatives of compounds originally isolated from natural products. There is evidence that extracts of Tulbaghia violacea can be used to treat cancer. The activation of apoptosis in cancer cells is a target for the development of novel anti-cancer drugs since one of the characteristics of cancer cells is resistance to apoptosis due to the deregulation of biochemical pathways leading to apoptosis. In fact, many current anti-cancer drugs exert their
effects through the activation of apoptosis. Previous studies showed that extracts of T.violacea induce apoptosis in cancer cells and one study reported on the isolation of a compound (methyl-Ô-D-glucopyranoside), which is responsible for the pro-apoptotic activity of the T.violacea extract. Therefore the aim of this study was to investigate the anti-cancer activity of methyl-Ô-Dglucopyranoside and extracts prepared from T.violacea. In this study the pro-apoptotic activity of
methyl-Ô-D-glucopyranoside and extracts prepared from T.violacea were investigated on a panel of human cancer cell lines, which included HepG2, MCF7, H157, HT29 and the non-cancerous cell line, KMST6. The induction of apoptosis was evaluated by flow cytometry using several bioassays which measures biochemical events (caspase activation, phosphatidylserine externalisation and reactive oxygen species (ROS) production that is associated with the induction of apoptosis. The
results demonstrated that the effects of methyl-ï¡-D-glucopyranoside on cultured cells are transient and that the cells recover from the effects of methyl-ï¡-D-glucopyranoside. This suggested thatmethyl-Ô-D-glucopyranoside is not the compound responsible for the pro-apoptotic bioactivity in the T.violacea extract. This study also showed that cytotoxic and pro-apoptotic bioactivity of the leaf-extract was significantly higher in comparison to the tuber-extract. The bioactivity of the organic solvent extracts (dichloromethane, hexane, methanol and 50% methanol/water) of T.violacea leaves was also significantly higher than water extracts of T.violacea leaves. A comparison of the different organic extracts prepared from the T.violacea leaves showed that the highest activity was observed for the dichloromethane and hexane extracts. In an effort to identify the bioactive compound(s) the dichloromethane extract was subjected to Versaflash® column chromatography. However, due to problems experienced with the solubility of the dichloromethane
sub-fractions, these compounds could not be tested for their bioactivity. Palmitone (16-hentriacontanone) was identified as one of the major compounds present in the dichloromethane sub-fractions. This compound was previously shown to have anticonvulsant bioactivity but there is no evidence in the literature that it has anti-cancer or pro-apoptotic activities. Fingerprinting of the methanol extract showed the presence of long chain fatty acid derivatives, flavonoids and allicin derivatives in the methanol extract. Although, this study failed to isolate the pro-apoptotic bioactive
compound(s) present in the extracts of T.violacea, it confirmed that extracts of this plant induce apoptosis in cultured human cancer cell lines.
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Disease mechanisms in the C3H/HeJ Mouse Model of AlopeciaBarekatain, Armin 05 1900 (has links)
Alopecia areata (AA) is a chronic inflammatory disease of hair follicles manifesting as
patchy areas of hair loss on the scalp and body. Development of AA is associated with
pen- and intra-follicular inflammation of anagen stage hair follicles, primarily by CD4+
and CD8+ cells. We hypothesized that if cell-mediated cytotoxicy against hair follicles is
to be a component of the hair loss disease mechanism, increased expression of genes and
products typical of cytotoxic cells, as well as increased apoptosis activity within affected
hair follicles, would be expected to occur in the lesional skin compared to the normal
skin. Furthermore, we studied gene expression levels of multiple cytokines and
characteristic chemokines, using the C3FI/HeJ mouse model of AA. mRNA expression
levels of granzyme A, granzyme B, perform Fas, Fas ligand, TNF-cL, TNF-aRl and R2,
TRAIL, TRAILR, TRAMP, Thi-, Th2-, and Th17-associated cytokines, as well as
multiple chemokines were compared between the skin, draining lymph nodes, thymus
and spleens of normal and AA-affected mice using quantitative reverse transcriptase
PCR. FasL, granzyme A, granzyme B, pro- and anti-inflammatory cytokines were all
highly up-regulated in the skin of AA-affected mice. Immunohistochemical studies of the
skin revealed that, although greater numbers of granzyme B and FasL expressing cells
were present in AA affected skin, the cells were morphologically diffusely distributed
and not exclusively located within the focal pen- and intrafollicular infiltrate. The
majority of these cells were further characterized as mast cells, which were also found in
substantially greater numbers in the skin of mice with AA compared to their normal
haired controls. Almost no perform expressing cells were identified in AA affected
mouse skin and TUNEL staining suggested relatively limited apoptosis activity in hair
follicle keratinocytes. In conclusion, while granzymes and FasL may play important roles
in disease development, the profiles and patterns of expression are not consistent with
direct cell-mediated cytotoxic action against the follicular epithelium in chronic mouse
AA. Potentially, hair growth inhibiting cytokines may play a more dominant role in AA
development than previously thought. Furthermore, mast cells, with their increased
presence around hair follicles in the AA affected mouse skin and their ability to express
granzyme B and FasL, are suggested as potential key players in the pathogenesis of AA.
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Chemical and biological investigation into some selected African indigenous medicinal plantsJelili Olalekan Babajide January 2009 (has links)
<p>African medicinal plants are commonly used throughout Africa to treat a variety of ailments including wounds and ulcers, cough and chest complaints, gingivitis, fever and gonorrhoea, indication all related to infection and inflammation. In screening several plant species from an inventory of common medicinal plants from both South and West Africa for diverse medicinal purposes, 6 plants were selected because of their interesting and useful ethnomedicinal values.</p>
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Screening of natural products and Alkylating agents for Antineoplastic ActivityKanyanda, Stonard Sofiel Elisa January 2007 (has links)
<p>Background and objectives: Apoptosis is a process in which a cell programmes its own death. It is a highly organized physiological mechanism in which injured or damaged cells are destroyed. Apart from physiological stimuli however, exogenous factors can induce apoptosis. Many anti-cancer drugs work by activating apoptosis in cancer cells. Natural substances have been found to have the ability to induce apoptosis in various tumour cells and these substances have been used as templates for the construction of  / novel lead compounds in anticancer treatment. On the other hand, alkylating agents such as cisplatin, cis- [PtCl2 (NH3) 2] have been widely used as antineoplastic agents for a  / wide variety of cancers including testicular, ovarian, neck and head cancers, amongst others. However, the use of cisplatin as an anticancer agent is limited due to toxicity and resistance problems. The aim of this present study was to screen the leaves of Rhus laevigata, a South African indigenous plant, for the presence of pro-apoptotic and  / anti-proliferative natural compounds and also to screen newly synthesised palladium based complexes (15 and 57) and a platinum based complex (58) for their antineoplastic  / activities tested against a panel of cell lines. Results. The results showed that crude methanol extracts from Rhus laevigata as well as the newly synthesised palladium based complexes (15 and 57) and a platinum based complex (58) induced apoptosis in the cell lines tested, as demonstrated by the externalization of phosphatidylserine, mitochondrial membrane permeabilization,caspase-3 activation, and DNA fragmentation. Caski (cervical cancer) and H157 (non small cell lung carcinoma) cell lines treated with the methanol extract from Rhus laevigata however, were more resistant to apoptosis induction. Among the metallocomplexes, complexes 15 and 57, palladium based complexes, were the most active. Conclusion: The methanol extract from the leaves of Rhus laevigata contain pro-apoptotic and antiproliferative natural compound(s), which need to be characterised and elucidated as they could provide the much-needed lead compounds in the fight against cancer. On the other hand the newly synthesized palladium complexes also need further evaluation to  / see if they can be used as anticancer agents that can overcome the problems associated with cisplatin.</p>
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The screening of phyto-pesticides for potential adverse effects on human healthShoko, Yeukai Phoebe January 2010 (has links)
<p>Pesticides are designed to control or eliminate pests such as insects, rodents, weeds,<br />
bacteria, and fungi. They are used at a global scale for agricultural produce. Although<br />
pesticides play a significant role in increasing food production and eliminating diseases,<br />
exposure to pesticides may be harmful to non-target organisms. As a result concern over<br />
safety and resistance to pesticides has increased and there is pressure to reduce use and<br />
search for more environmentally and toxicologically safe and efficacious pesticides. Most<br />
pesticides currently in use are synthetic / therefore an alternative to synthetic pesticides is<br />
the use of naturally occurring products/ botanicals with pesticidal properties.</p>
<p>Two plants indigenous to South African with pesticidal properties were chosen for this<br />
study. Dicerothamnus rhinocerotis (D. rhinocerotis) and Galenia africana (G. africana)<br />
have potential antifungal properties thus, may have potential use on agricultural produce<br />
as fungicides. Galenia africana and D. rhinocerotis extracts inhibit growth of B. cinerea<br />
(a fungal pathogen) at concentrations greater than 31.25 mg/ml and 125mg/ml<br />
respectively. A major consideration in approving pesticides for use is whether they pose<br />
an unreasonable risk to humans and to the environment. Toxicity studies are required to<br />
determine the safety of the plant extracts.</p>
<p>The purpose of this study was to evaluate potential toxicity of ethanol extracts of D.<br />
rhinocerotis and G. africana, which is important when designing practices to reduce or<br />
eliminate excess exposure to them. Natural plant products with pesticidal properties could<br />
provide an alternative to synthetic pesticides and may thus effectively reduce resistance<br />
levels.<br />
<br />
<br />
  / </p>
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Le récepteur de l'IL-7 sur les cellules NK matures humaines : nature et fonctionMichaud, Annie January 2008 (has links)
Mémoire numérisé par la Division de la gestion de documents et des archives de l'Université de Montréal
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Self-healing Poly(methyl methacrylate) Bone Cement Utilizing Embedded Microencapsulated 2-Octyl Cyanoacrylate Tissue AdhesiveBrochu, Alice January 2013 (has links)
<p>Extending the functional lifetime of acrylic poly(methyl methacrylate) (PMMA) bone cement may reduce the number of revision total joint replacement (TJR) surgeries performed each year. We developed a system utilizing an encapsulated water-reactive, FDA-approved tissue adhesive, 2-octyl cyanoacrylate (OCA), as a healing agent to repair microcracks within a bone cement matrix. The proposed research tested the following hypotheses: (1) reactive OCA can be successfully encapsulated and the resulting capsules thoroughly characterized; (2) the static mechanical properties of the PMMA composite can be improved or maintained through inclusion of an optimal wt% of OCA-containing capsules; (3) PMMA containing encapsulated OCA has a prolonged lifetime when compared with a capsule-free PMMA control as measured by the number of cycles to failure; and (4) the addition of capsules to the PMMA does not significantly alter the biocompatibility of the material. Based on the experiments reported herein, the primary conclusions of this dissertation are as follows: (1) functional OCA can be encapsulated within polyurethane spheres and successfully incorporated into PMMA bone cement; (2) lower wt% of capsules maintained the tensile, compressive, fracture toughness, and bending properties of the PMMA; (3) inclusion of 5 wt% of OCA-containing capsules in the matrix increased the number of cycles to failure when compared to unfilled specimens and those filled with OCA-free capsules; and (4) MG63 human osteosarcoma cell proliferation and viability were unchanged following exposure to OCA-containing PMMA when compared with a capsule-free control.</p> / Dissertation
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Investigating the Relationship Between Structure, Ice Recrystallization Inhibition Activity and Cryopreservation Ability of Various Galactopyranose DerivativesTokarew, Jacqueline 31 May 2011 (has links)
The goal of our research is to generate cryopreservation agents derived from antifreeze
glycoproteins. One postulated mechanism of cell cryo-injury is ice recrystallization. It is known that simple saccharides and cryopreservation agents (DMSO) display ice recrystallization inhibition (IRI). This study assessed the cytotoxicity and cryopreservation ability of these sugars in relation to their IRI. It was determined that compounds with greater IRI have increased cytotoxicity yet confer cryoprotection. To further investigate how structure is affecting IRI activity, several galactopyranoside derivatives were synthesized. A series of deoxy and α-Callyl-
deoxy galactopyranoses were prepared. Testing determined that removal of any hydroxyl
group removes IRI. 3-deoxy-β-thiophenyl galactose was also synthesized and had surprisingly better IRI than β-thiophenylgalactose. Also, 6-azido galactose had similar IRI to 6-deoxy galactose. Lastly, a series of β- thioalkylgalactosides was synthesized and testing gave contradicting results which suggest that predicting IRI based on hydrophilicity is more complicated than initially hypothesized.
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Baltymų frakcijų, praturtintų lektinais, išskirtų iš Urtica dioica L. žolės, antimutageninio, citotoksinio ir antioksidacinio aktyvumo tyrimas / Investigation of antimutagenic activity, cytotoxicity and antioxidant activity in lectin-enriched protein fractions from herb of Urtica dioica LStaršelskytė, Rasa 30 June 2014 (has links)
R. Staršelskytės magistro baigiamasis darbas/ mokslinė vadovė prof. N. Savickienė;
Konsultantės: dr. Annabella Vitalone, prof. Gabriela Mazzanti, dr. Antonella Di Sotto;
Lietuvos sveikatos mokslų universiteto, Farmacijos fakulteto, Farmakognozijos katedra. – Kaunas.
Romos universiteto La Sapienza, Fiziologijos ir farmakologijos katedra. – Roma.
Darbo tikslas: baltymų frakcijų, praturtintų lektinais, išskirtų iš Urtica doica L. žolės, antimutageninio, citotoksinio ir antioksidacinio aktyvumo įvertinimas.
Darbo uždaviniai:
1. Įvertinti Urtica dioica L. baltymų frakcijų įtaką Salmonella typhimurium ir Escherichia coli kamienų mutageniškumui, naudojant AMES testo metodą.
2. Ištirti Urtica dioica L. baltymų frakcijų citotoksiškumą HepG2 ląstelių proliferacijai, naudojant MTT dažo redukcijos reakcijos metodą.
3. Ištirti Urtica dioica L. baltymų frakcijų antioksidacinį aktyvumą, naudojant modelinius ABTS (2,2-azino-bis-(3-etilbenztiazolin-6-sulfono rūgšties)) ir superoksido radikalus.
Metodai:
1. Lektinais praturtintų baltymų frakcijų antimutageniškumas tiriamas AMES testo metodu (grįžtamosios mutacijos modeliu in vitro) su S9 metabolinės aktyvacijos sistema (supernatantu iš žiurkių (paveiktų fenobarbitalio/β-naftoflavono mišiniu) kepenų lątelių mitochondrijų) ir be S9 metabolinės aktyvacijos sistemos. Eksperimentui naudojami trys bakterijų kamienai: S. typhimurium TA98, S. typhimurium TA100 ir E. coli WP2uvrA.
2. Citotoksiškumas nustatomas MTT dažo redukcijos reakcijos metodu... [toliau žr. visą tekstą] / Rasa Staršelskytė master thesis/ Supervisor of the research paper: prof. Nijolė Savickienė1
Consultants: PhD Annabella Vitalone, prof. Gabriela Mazzanti, PhD Antonella Di Sotto2
1Department of Pharmacognosy, Faculty of pharmacy, Lithuanian University of Health Sciences, Lithuania
2Department of Physiology and Pharmacology, Sapienza University of Rome, Italy
Objective of work: evaluation of antimutagenicity, cytotoxicity and antioxidant activity of lectin-enriched protein fractions from herb of Urtica dioica L.
Main tasks:
1. To evaluate antimutagenic activity of lectin-enriched protein fractions by bacterial reverse mutation assay.
2. To determine cytotoxicity of lectin-enriched protein fraction by the tetrazolium dye (MTT) colorimetric assay.
3. To evaluate antioxidant activity of lectin-enriched protein fraction against ABTS-free radical and superoxide-radical.
Methods:
1. The antimutagenicity was studied in a bacterial reverse mutation assay (Ames test), both in the absence and presence of an exogenous metabolic activator S9 (the liver postmitochondrial supernatant of rats treated with the mixture phenobarbital/β-naphthoflavone to induce the hepatic microsomal enzymes). A set of three strains, S. typhimurium TA98, S. typhimurium TA100 and E. coli WP2uvrA, was used.
2. Cytotoxicity was determined by the tetrazolium dye (MTT) colorimetric assay in HepG2 human hepatoblastoma cell line.
3. The antioxidant activity was evaluated by ABTS-free radical scavenging activity test... [to full text]
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Hepatocyte Cytotoxicity Induced by Hydroperoxide (Oxidative Stress Model) or Dicarbonyls (Carbonylation Model): Prevention by Bioactive Nut Extracts or CatechinsBanach, Monica Sofia 16 December 2009 (has links)
Carbonyl and oxidative stress augment the development of diabetic complications. We evaluated the cytoprotectiveness of walnut and hazelnut extracts and catechins for decreasing cytotoxicity, lipid peroxidation, reactive oxygen species (ROS) formation, and protein carbonylation in cell death models of carbonyl and oxidative stress. Polar extracts (methanol or water) showed better cytoprotection than the non-polar (ethyl acetate) nut extracts against hydroperoxide-induced hepatocyte cell death and oxidative stress markers. Catechin flavonoids found in plants, including walnuts and hazelnuts, prevented serum albumin carbonylation in a carbonyl stress model (using glyoxal or methylglyoxal). Hepatocyte protein carbonylation and cell death were prevented and UV spectra data suggested a catechin:methylglyoxal adduct was formed. We conclude that (a) bioactive nut constituents in polar extracts were more protective than non-polar extracts against oxidative stress, and (b) catechins were effective under physiological temperature and pH, at preventing dicarbonyl induced cytotoxicity likely by trapping dicarbonyls or reversing early stage carbonylation.
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