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Spices

Spices are aromatic and flavorful plant-derived substances used to enhance the taste and aroma of foods.
They are commonly derived from the seeds, fruits, roots, or bark of various plants and have been used in culinary and medicinal applications for centuries.
Spices can add depth, complexity, and nuance to dishes, and may also possess antioxidant, anti-inflammatory, and antimicrobial properties.
Common examples include black pepper, cinnamon, ginger, turmeric, and chili peppers.
Spices play a key role in many cuisines around the world and can be an important component of a healthy, balanced diet when used in moderation.
Reserach into the potential health benefits and optimal culnary applications of spices is an area of active study.

Most cited protocols related to «Spices»

Data used in this manuscript are either artificial (Figure 2), or from studies of HIV-specific T cell representation in infected subjects collected in our laboratory. Standard intracellular cytokine staining assays were used. As all data are purely for illustration of algorithms and displays, thus no information about the subjects nor assay results is provided. All human samples were collected under NIAID IRB approval. Flow cytometry data was analyzed using FlowJo v9.1 (TreeStar, Inc., Ashland, OR). Background subtraction and formatting of exported data from FlowJo was performed with Pestle v1.6.2 (see below). Statistical analysis and display of multicomponent distributions was performed with SPICE v5.1 (freely available from http://exon.niaid.nih.gov/spice/).
Publication 2011
Biological Assay Cytokine Exons Flow Cytometry Homo sapiens Protoplasm Spices T-Lymphocyte
A significant power of SPICE is the ability to easily navigate complex data to show distributions and calculate statistics on subsets of measurements grouped, overlaid, or compared on the basis of different categorical descriptors. Many such descriptors are not necessarily part of the exported flow cytometry data, such as demographic or other patient information. To facilitate the analysis of such datasets, we created the data pre-processing program. Pestle handles such functions as background subtraction (e.g., for functional data), editing of the primary dataset, creation of additional categorical variables (such as “number of functions”), and merging other databases to provide additional categorical descriptors for each sample. Pestle is freely available by request from MR.
Publication 2011
Flow Cytometry Patients Spices
The 14-page questionnaire was designed to capture the habitual food intake among Norwegian adults the preceding year. The FFQ was an extended and revised version of the semi-quantitative food-frequency questionnaire used in the Norwegian nation wide survey NORKOST 1997 (NFFQ). The original NFFQ was a validated, 180 items optical readable FFQ, developed to cover 100% of the total EI of the population [3 -6 (link)]. Based on our extensive screening of antioxidant content in foods and beverages [7 (link)], the NFFQ was updated and revised with questions about food products and food categories assumed to be important sources of antioxidant intake in Norway. The new FFQ included 270 food items, grouped together according to the Norwegian meal pattern. Additional questions were added concerning intake of several food categories. In detail, 19 questions about berries, 4 questions about fruit, 6 questions about vegetables, 2 questions about chocolate, 3 questions about coffee and 2 questions about tea were added. Questions concerning the variable intake of berries due to seasonal variations were included. Furthermore, 10 questions were added about nuts and seeds and 27 questions about spices and herbs. The options of frequency of consumption of particular food items varied from several times a day to never/seldom, with portion sizes based on typical household units: slices, glasses, cups, pieces, spoons and teaspoons. When frequency was answered but not portion size, the food item was given the smallest portion size. When portion size was answered but not frequency, the food item was given the value zero. One participant was excluded from the study because a substantial amount of the questions in the FFQ were left unanswered. The dietary questions totaled 11 pages of the questionnaire whereas the last 3 pages were dedicated to questions concerning dietary supplements, smoking, physical activity and past and present illnesses and medication. The answered FFQs were scanned and the image files translated into data files using the Cardiff Teleform 2006 software.
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Publication 2010
Adult Antioxidants Berries Beverages Chocolate Coffee Diet Dietary Supplements Eating Eyeglasses Food Fruit Households Nuts Pharmaceutical Preparations Plant Embryos Spices Vegetables Vision
The present work proposes a novel analytical tool for complex combinatorial datasets. It is essentially theoretical, but makes use of three experimental datasets to illustrate the power of the analysis. One experimental dataset was derived from a previously published study. [11] Of note, pie charts presented in Figure 3 derive from this study. The pro-inflammatory IL-17A- and IL-22-secreting CD4+ T cell responses of 25 healthy individuals were analyzed as previously described. [15] (link) Similarly, HIV-specific responses of 26 untreated HIV-infected patients were analyzed by the same technical approach as previously described by us for CMV-specific responses. [38] (link) The methodologies behind the datasets are therefore only briefly described here. Peripheral Blood Mononuclear Cells (PBMCs) were purified and stimulated with either 1 µg/ml PMA and 1 µg/ml Ionomycin (Sigma-Aldrich, France), EBV peptide antigen (5 µM) or HIV-gag p17 overlapping peptides (5 µM each) at 37°C. Cytokine secretion was blocked with 2.5 µg/ml monensin and 5 µg/ml brefeldin A (Sigma-Aldrich). After 16 h of stimulation, cells were incubated with directly conjugated anti-CD4-APC/Cy7 (BD Biosciences, San Jose, CA), anti-CD8-Alexa405 (Caltag, Burlingame, CA) and when appropriate PE-conjugated EBV peptide-MHC class I tetramer. Cells were permeabilized with Cytofix/Cytoperm™ (BD Biosciences) and stained with anti-cytokine antibodies for 20 minutes at room temperature. Finally, 106 cell events were analyzed on a BD LSRII apparatus using FACSDiva (BD Biosciences) and FlowJo (TreeStar Inc) softwares. Polyfunctionality analysis was performed using Pestle Version 1.6.2 and Spice Version 4.2.3 (Mario Roederer, ImmunoTechnology Section, VRC/NIAID/NIH). [25]
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Publication 2012
Anti-Antibodies Antigens Brefeldin A CD4 Positive T Lymphocytes Cells Cytokine Genes, MHC Class I IL17A protein, human IL25 protein, human Inflammation Ionomycin Monensin P17 peptide Patients PBMC Peripheral Blood Mononuclear Cells Peptides secretion Spices Tetrameres
We used the high-resolution spatiospectral numerical phantom described in (30 (link)) for our simulation study. The phantom has 128 × 128 matrix size and 512 time points sampled at a bandwidth of 1200 Hz, and contains spatial distributions of commonly observed 1H metabolites (see (30 (link)) for a more detailed description). We generated (k, t)-space measurements from this phantom with or without field inhomogeneity effects introduced through a coregistered in vivo ΔB0 map according to Eq. [1]. A simulated full data set without the field inhomogeneity effects was used as the gold standard to compare three acceleration methods: (i) SPICE, (ii) low-resolution CSI, and (iii) EPSI (7 (link)). The effect of field inhomogeneity was included for all three schemes, which were set up to have the same acquisition time. Additional noise was added into the simulated EPSI data to account for the SNR difference due to different readout bandwidths. The field inhomogeneity corrected conjugate phase (CP) algorithm (31 ) was used to obtain the CSI and EPSI reconstructions, which are compared with the corresponding SPICE reconstructions.
Publication 2014
Acceleration Gold Reconstructive Surgical Procedures Spices

Most recents protocols related to «Spices»

Fresh mutton hindleg meat and tail fat were obtained from a local commercial processor (Hohhot, China), and sausages were made with modifications to the method previously described47 (link). The sausage's ingredients were as follows: mutton hindleg meat (70%), mutton tail fat (30%), salt (2.5%), glucose (0.5%), sugar (1%), NaNO2 (0.01%), ascorbic acid (0.05%), pepper powder (0.2%), ginger powder (0.2%), spice powder (0.1%), corn starch (1%), and lactalbumin powder (0.5%). The ingredients were thoroughly mixed and filled into pig casings. The sausage diameter was approximately 3 cm, and length was approximately 20 cm. Control was fermented sausage without starter culture and the treatment was fermented sausage inoculated with L.fermentum 332 (the concentration of the starter culture was 4%, 106 CFU/g). For 24 h, fermentation was carried out at 30 °C and 95% relative humidity (day 1). This was known as the fermentation period. For four days, the sausages were placed in a 15 °C and 75–85% relative humidity environment (day 5). This stage was regarded as the drying period. Then, the sausages were transferred to an environment of 10 °C and 65% relative humidity for 6 days (day 11). This stage was regarded as the maturation period. After preparation, the samples were packed and stored at − 20 °C until further analyses. The sausages in both groups were sampled at various fermentation times (day 1, 5, and 11) to determine AI-2 activity, LAB viable count, physicochemical characteristics, and volatile flavor components.
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Publication 2023
Ascorbic Acid Carbohydrates Cornstarch Fermentation Flavor Enhancers Glucose Humidity Lactalbumin Meat Piper nigrum Powder Sodium Chloride Spices Tail Zingiber officinale
Process waters generated
during various steps of herring processing were collected at Sweden
Pelagic AB in Ellös, Sweden, as follows: (i) RSW from herring
storage on board a boat was collected in March 2020, (ii) salt brines
(13% NaCl) from presalting of herring skin-on fillets or deskinned
fillet pieces were collected in the North Sea (October 2018), and
(iii) marination brines into which the presalted herring is placed
and stored for up to 2 years: (a) salt marination brine (SMB), (b)
spice marination brine (SPB), and (c) vinegar marination brine (VMB).
Mussel (Mytilus edulis) processing
at Vilsund Blue, Nykobing Mors, Denmark, comprises four different
steps: boiling, removal of impurities through treatment with 15% salt
brine, vibration to remove the shells, and a final rinsing step to
remove salt residues. The four different process waters collected
for this study were boiling water (generated during boiling mussels),
juice (generated during dripping of the boiling water from mussels
when transferred on a belt to the next step), salt brine (generated
during brining with salt brine), and rinsing brine (generated while
mussels are rinsed to remove salt). Mussel process waters were sampled
in 2016 and 2017.
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Publication 2023
brine moira protein, Drosophila Mussels Mytilus edulis Skin Sodium Chloride Spices Vibration Vinegar

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Publication 2023
Coffee Condiments Food Spices
The study was approved by the Ethical Committee of the First Affiliated Hospital (Xijing Hospital) of the Fourth Military Medical University, with approved numbers KY20212173 and NCT05155358. All procedures relating to human participants were performed following the Declaration of Helsinki. All participants signed an informed consent form. The inclusion criteria were: male military personnel aged 18–35. The exclusion criteria were: participants who smoked, were injured, or had a history of gastrointestinal, lung, heart, or kidney diseases. Finally, 32 healthy male soldiers with an average age of (24.59 ± 5.36) years took part in this study. The participants received training in the same base for nearly 2 years, and their living environments were similar. All participants did not take any drugs 3 months before and during the experiments. The homogenization process was performed for 7 days with the same daily training and lives. Meals were served in the same cafeteria with a relatively fixed menu and no spicy food. Smoking and drinking were prohibited.
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Publication 2023
Food Heart Homo sapiens Kidney Diseases Lung Males Military Personnel Pharmaceutical Preparations Soldiers Spices
Data entry was done by using Microsoft Access and data analysis was done by STATA (version 14). Dietary diversity score was determined by adding the number of food categories consumed by each participant over the previous 24 hours. The questionnaire contained 16 food groups. The 16 food groups were—cereals; white roots and tubers; vitamin A-rich vegetables and tubers; dark green leafy vegetables; other vegetables; vitamin A-rich fruits, other fruits; organ meat; flesh meats; eggs; fish and seafood; legumes; nuts and seeds; milk and milk products; oils and fats; sweets, spices, condiments, and beverages. We combined certain food groups into a single food group for analytical purposes. We analyzed 9 food groups for measuring individual dietary diversity score. Dietary diversity score ranged from 0 to 9. According to the guideline, when we aggregated two food groups into one, any of the food group’s “Yes” answer is considered as “Yes” for that aggregated group and numbered as “1” for the respected group. According to the guidelines, there is no established cut-off point in terms of food groups to indicate adequate or inadequate dietary diversity [27 ]. For this, we calculated the mean dietary diversity score for analytical purpose.
Categorical variables were presented as frequency and percentage. Continuous variables were presented as mean with standard deviation. To see the relationship with the study group, we performed t-test for normally distributed data and Mann-Whitney test for skewed data. As the dietary diversity score was incomparable between the control and intervention arm at baseline, difference-in-difference (DID) analysis was performed to assess the effect of the intervention. During performing the DID we adjusted for adolescent’s age, adolescent girls’ father’s age, years of schooling of caregiver, adolescents’ father’s years of schooling, household’s monthly income, household head’s occupation and asset index.
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Publication 2023
Adolescent Adolescent Fathers Adolescents, Female Beverages Cereals Condiments Diet Eggs Fabaceae Fats Fishes Food Fruit Head of Household Households Meat Milk, Cow's Nuts Oils Plant Embryos Plant Leaves Plant Roots Plant Tubers Seafood Spices Vegetables Vitamin A Woman

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More about "Spices"

Spices are aromatic plant-derived substances used to enhance the taste and aroma of foods.
They are commonly derived from the seeds, fruits, roots, or bark of various plants and have been used in culinary and medicinal applications for centuries.
Spices can add depth, complexity, and nuance to dishes, and may also possess antioxidant, anti-inflammatory, and antimicrobial properties.
Common examples include black pepper, cinnamon, ginger, turmeric, and chili peppers.
Research into the potential health benefits and optimal culinary applications of spices is an active area of study.
Spices play a key role in many cuisines around the world and can be an important component of a healthy, balanced diet when used in moderation.
When it comes to conducting research on spices, tools like the LSRII flow cytometer, GolgiStop, LSRFortessa, Cytofix/Cytoperm, and GolgiPlug can be useful for analyzing the bioactive compounds and their effects.
The FACSDiva software, GraphPad Prism 5, Prism 8, Prism 6, and Prism 9 can also be leveraged for data analysis and visualization.
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