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1.
Histol Histopathol ; 38(9): 989-997, 2023 Sep.
Article in English | MEDLINE | ID: mdl-36896890

ABSTRACT

AIMS: Pancreatic adenocarcinoma represents a therapeutic challenge due to the high toxicity of antineoplastic treatments and secondary effects of pancreatectomy. T-514, a toxin isolated from Karwinskia humboldtiana (Kh) has shown antineoplastic activity on cell lines. In acute intoxication with Kh, we reported apoptosis on the exocrine portion of pancreas. One of the mechanisms of antineoplastic agents is the induction of apoptosis, therefore our main objective was to evidence structural and functional integrity of the islets of Langerhans after the administration of Kh fruit in Wistar rats. METHODS: TUNEL assay and immunolabelling against activated caspase-3 were used to detect apoptosis. Also, immunohistochemical tests were performed to search for glucagon and insulin. Serum amylase enzyme activity was also quantified as a molecular marker of pancreatic damage. RESULTS: Evidence of toxicity on the exocrine portion, by positivity in the TUNEL assay and activated caspase-3, was found. On the contrary, the endocrine portion remained structurally and functionally intact, without apoptosis, and presenting positivity in the identification of glucagon and insulin. CONCLUSIONS: These results demonstrated that Kh fruit induces selective toxicity on the exocrine portion and establish a precedent to evaluate T-514 as a potential treatment against pancreatic adenocarcinoma without affecting the islets of Langerhans.


Subject(s)
Adenocarcinoma , Islets of Langerhans , Karwinskia , Pancreatic Neoplasms , Rats , Animals , Rats, Wistar , Karwinskia/toxicity , Caspase 3/metabolism , Glucagon/metabolism , Adenocarcinoma/drug therapy , Adenocarcinoma/metabolism , Fruit/toxicity , Pancreatic Neoplasms/drug therapy , Pancreatic Neoplasms/metabolism , Islets of Langerhans/metabolism , Insulin , Pancreatic Neoplasms
2.
Biofabrication ; 14(3)2022 04 21.
Article in English | MEDLINE | ID: mdl-35344936

ABSTRACT

Cancer continues to be a leading cause of mortality in modern societies; therefore, improved and more reliablein vitrocancer models are needed to expedite fundamental research and anti-cancer drug development. Here, we describe the use of a miniaturized continuous stirred tank reactor (mCSTR) to first fabricate and mature cancer spheroids (i.e. derived from MCF7 cells, DU145 cells, and a mix of MCF7 cells and fibroblasts), and then to conduct anti-cancer drug assays under continuous perfusion. This 3 ml mCSTR features an off-center agitation system that enables homogeneous chaotic laminar mixing at low speeds to support cell aggregation. We incubated cell suspensions for 3 d in ultra-low-attachment plates to allow formation of discoid cell aggregates (∼600µm in diameter). These cell aggregates were then transferred into mCSTRs and continuously fed with culture medium. We characterized the spheroid morphology and the expression of relevant tumor biomarkers at different maturation times for up to 4 weeks. The spheroids progressively increased in size during the first 5-6 d of culture to reach a steady diameter between 600 and 800µm. In proof-of-principle experiments, we demonstrated the use of this mCSTR in anti-cancer drug testing. Three drugs commonly used in breast cancer treatment (doxorubicin, docetaxel, and paclitaxel) were probed at different concentrations in MCF7-derived spheroids. In these experiments, we evaluated cell viability, glucose consumption, spheroid morphology, lactate dehydrogenase activity, and the expression of genes associated with drug resistance (ABCB1andABCC1) and anti-apoptosis (Bcl2). We envision the use of this agitated system as a tumor-on-a-chip platform to expedite efficacy and safety testing of novel anti-cancer drugs and possibly in personalized medicine applications.


Subject(s)
Antineoplastic Agents , Breast Neoplasms , Antineoplastic Agents/pharmacology , Cell Line, Tumor , Cell Survival , Female , Humans , Printing, Three-Dimensional , Spheroids, Cellular
3.
Lipids Health Dis ; 17(1): 128, 2018 May 29.
Article in English | MEDLINE | ID: mdl-29843731

ABSTRACT

BACKGROUND: Excessive subcutaneous adiposity in obesity is associated to positive white adipocyte tissue (WAT) differentiation (adipogenesis) and WAT expandability. Here, we hypothesized that supplementation with the insulin inhibitor and mitochondrial uncoupler, Tyrphostin (T-AG17), in vitro and in vivo inhibits adipogenesis and adipocyte hypertrophy. METHODS: We used a 3T3-L1 proadipocyte cell line to identify the potential effect of T-AG17 on adipocyte differentiation and fat accumulation in vitro. We evaluated the safety of T-AG17 and its effects on physiological and molecular metabolic parameters including hormonal profile, glucose levels, adipogenesis and adipocyte hypertrophy in a diet-induced obesity model using C57BL/6 mice. RESULTS: We found that T-AG17 is effective in preventing adipogenesis and lipid synthesis in the 3T3-L1 cell line, as evidenced by a significant decrease in oil red staining (p < 0.05). In obese C57BL/6 mice, oral administration of T-AG17 (0.175 mg/kg for 2 weeks) lead to decreased fat accumulation and WAT hypertrophy. Further, T-AG17 induced adipocyte apoptosis by activating caspase-3. In the hepatocytes of obese mice, T-AG17 promoted an increase in the size of lipid inclusions, which was accompanied by glycogen accumulation. T-AG17 did not alter serum biochemistry, including glucose, insulin, leptin, free fatty acids, creatinine, and aspartate aminotransferase. CONCLUSION: T-AG17 promotes adipocyte apoptosis in vivo and is an effective modulator of adipocyte differentiation and WAT hypertrophy in vitro and in vivo. Therefore, T-AG17 may be useful as a pharmacological obesity treatment.


Subject(s)
Adipocytes, White/metabolism , Adipogenesis/drug effects , Lipid Metabolism , Nitriles/pharmacology , Obesity/drug therapy , 3T3-L1 Cells , Adipocytes, White/drug effects , Adipocytes, White/physiology , Animals , Apoptosis , Diet, High-Fat , Male , Mice , Mice, Inbred C57BL , Mice, Obese , Obesity/metabolism , Obesity/physiopathology , Uncoupling Agents/pharmacology
4.
Histol Histopathol ; 31(9): 1001-10, 2016 Sep.
Article in English | MEDLINE | ID: mdl-26877198

ABSTRACT

Karwinskia humboldtiana (Kh) is a poisonous plant that grows in some regions of the American continent. Consuming large amounts of Kh fruit results in acute intoxication leading to respiratory failure, culminating in death within days. There is evidence of histological damage to the lungs, liver, and kidneys following accidental and experimental Kh intoxication. To date, the microscopic effect of Kh consumption on the pancreas has not been described. We examined the early effects of Kh fruit on pancreatic tissue at different stages of acute intoxication in the Wistar rat. We found progressive damage confined to the exocrine pancreas, starting with a reduction in the number of zymogen granules, loss of acinar architecture, the presence of autophagy-like vesicles, apoptosis and inflammatory infiltrate. The pancreatic pathology culminated in damaged acini characterized by necrosis and edema, with a complete loss of lobular architecture. Interestingly, the morphology of the islets of Langerhans was conserved throughout our evaluations. Taken together, our results indicate the damage induced by a high dose of Kh fruit in the Wistar rat is consistent with an early acute necrotizing pancreatitis that exclusively affects the exocrine pancreas. Therefore, this system might be useful as an animal model to study the treatment of pancreatic diseases. More importantly, as the islets of Langerhans were preserved, the active compounds of Kh fruit could be utilized for the treatment of acinar pancreatic cancer. Further studies might provide insight into the severity of acute Kh intoxication in humans and influence the design of treatments for pancreatic diseases and acinar pancreatic cancer.


Subject(s)
Acinar Cells/pathology , Islets of Langerhans/pathology , Karwinskia/toxicity , Pancreatitis, Acute Necrotizing/pathology , Animals , Disease Models, Animal , Immunohistochemistry , Rats , Rats, Wistar
5.
PLoS One ; 10(4): e0122489, 2015.
Article in English | MEDLINE | ID: mdl-25859853

ABSTRACT

BACKGROUND: Foams are high porosity and low density materials. In nature, they are a common architecture. Some of their relevant technological applications include heat and sound insulation, lightweight materials, and tissue engineering scaffolds. Foams derived from natural polymers are particularly attractive for tissue culture due to their biodegradability and bio-compatibility. Here, the foaming potential of an extensive list of materials was assayed, including slabs elaborated from whole flour, the starch component only, or the protein fraction only of maize seeds. METHODOLOGY/PRINCIPAL FINDINGS: We used supercritical CO2 to produce foams from thermoplasticized maize derived materials. Polyethylene-glycol, sorbitol/glycerol, or urea/formamide were used as plasticizers. We report expansion ratios, porosities, average pore sizes, pore morphologies, and pore size distributions for these materials. High porosity foams were obtained from zein thermoplasticized with polyethylene glycol, and from starch thermoplasticized with urea/formamide. Zein foams had a higher porosity than starch foams (88% and 85%, respectively) and a narrower and more evenly distributed pore size. Starch foams exhibited a wider span of pore sizes and a larger average pore size than zein (208.84 vs. 55.43 µm2, respectively). Proof-of-concept cell culture experiments confirmed that mouse fibroblasts (NIH 3T3) and two different prostate cancer cell lines (22RV1, DU145) attached to and proliferated on zein foams. CONCLUSIONS/SIGNIFICANCE: We conducted screening and proof-of-concept experiments on the fabrication of foams from cereal-based bioplastics. We propose that a key indicator of foamability is the strain at break of the materials to be foamed (as calculated from stress vs. strain rate curves). Zein foams exhibit attractive properties (average pore size, pore size distribution, and porosity) for cell culture applications; we were able to establish and sustain mammalian cell cultures on zein foams for extended time periods.


Subject(s)
Biocompatible Materials , Carbon Dioxide , Zea mays , Animals , Cell Culture Techniques , Cell Line , Humans , Materials Testing , Mice , Porosity , Temperature , Zein
6.
Cir. & cir ; 66(6): 219-22, nov.-dic. 1998. tab, ilus
Article in Spanish | LILACS | ID: lil-243058

ABSTRACT

Evaluamos el efecto de la adventectomía perivascular (AP) sobre las anastomosis de los vasos mesentéricos de un modelo animal canino. Se efectuaron anastomosis término-terminal en un grupo experimental con AP y en un grupo control sin AP. El diámetro de los vasos se midió con angiografía antes y después del procedimiento en cada grupo y se registró la permeabilidad de la anastomosis. Después del procedimiento la diferencia de los diámetros entre los dos grupos de significativa (t=-5.893, pó0.0001). En el grupo control después del procedimiento hubo una pérdida de más de 50 por ciento del diámetro y el 20 por ciento de los casos se ocluyó. En el grupo experimental la pérdida de su diámetro fue del 20 por ciento y todas las anastomosis se mantuvieron permeables. Se concluye que la AP es un método útil para evitar los fenómenos vosoespásticos por la manipulación, el flujo sanguíneo se mantiene y la anastomosis continúa permeable


Subject(s)
Animals , Dogs , Anastomosis, Surgical/methods , Angiography , Laparotomy , Laparotomy/instrumentation , Microsurgery , Microsurgery/instrumentation , Data Interpretation, Statistical , Sympathectomy , Abdomen/surgery
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