Insulin sensitization: Enhances glucose uptake in adipocytes via Akt phosphorylation, independent of insulin .
Lipid metabolism: Correlates inversely with BMI, LDL cholesterol, and triglycerides .
Key pathways:
Inhibits TNF-α-induced COX-2 expression via JNK suppression .
Reduces NADPH oxidase activity → Decreases vascular oxidative stress .
Data from ELISA studies showing mean serum concentrations: 486 ng/ml (men), 434 ng/ml (women) .
ELISA specificity: Recognizes epitopes between residues 264–313 with <0.1% cross-reactivity to omentin-2 .
Matrix effects: Heparin plasma shows 103% recovery vs serum; avoid EDTA/citrate samples .
Metabolic disorders: Phase I trials exploring omentin supplementation in T2DM .
Cardiovascular disease: Preclinical models show 40% reduction in neointimal hyperplasia .
Inflammatory bowel disease: Murine studies demonstrate mucosal healing acceleration .
Human Intelectin-1/Omentin is derived from a preproprecursor that is 313 amino acids in length. The protein structure consists of:
An 18 amino acid signal sequence
A 280 amino acid mature segment (positions 19-298)
A 15 amino acid C-terminal segment
The mature protein has a molecular weight of approximately 34 kDa and is encoded by the gene with accession number Q8WWA0 . The protein is primarily produced by visceral adipose tissue, distinguishing it from many other adipokines that are predominantly expressed in subcutaneous adipose tissue .
Multiple validated techniques have demonstrated efficacy in detecting Omentin:
Immunohistochemistry/Immunofluorescence: Optimal concentrations range from 0.5-10 μg/mL using affinity-purified polyclonal antibodies. For example, sheep anti-human Intelectin-1/Omentin antibody at 5 μg/mL has shown specific staining in the cytoplasm of U937 human histiocytic lymphoma cells .
Tissue-specific localization: Fluorescent immunohistochemistry effectively identifies Omentin in goblet cells of the intestine, where it localizes to mucus granules .
Western Blotting: Recommended for protein quantification in tissue lysates.
ELISA: Primary method for measuring circulating levels in serum or plasma samples.
Multiple detection methods should be employed for cross-validation of results, particularly when investigating novel tissues or experimental conditions.
Omentin demonstrates distinct expression patterns across multiple tissues:
Intestinal tissues: Particularly in goblet cells of the ileum, where it localizes to mucus granules
Immune cells: Detected in the cytoplasm of U937 human histiocytic lymphoma cell line
Evolutionary conservation: Similar expression patterns observed in mouse intestine
This diverse expression profile suggests functions beyond metabolism, potentially including roles in mucosal immunity and intestinal barrier function.
Research consistently demonstrates significant relationships between Omentin levels and metabolic health:
The consistent inverse relationship between Omentin levels and metabolic disorders suggests its potential utility as a biomarker for metabolic health assessment .
Multiple lines of evidence establish Omentin's relationship with glucose homeostasis:
Decreased Omentin concentrations are observed in patients with impaired glucose regulation and diabetes (both type 1 and type 2) .
Inverse correlations exist between Omentin levels and insulin resistance markers .
Experimental Omentin-1 administration in high-fat diet-fed rats significantly decreased glucose, insulin, and HOMA-IR compared to untreated obese controls .
These findings suggest that Omentin likely improves insulin sensitivity through mechanisms that warrant further investigation in molecular signaling studies.
Emerging evidence supports dietary modification of Omentin levels:
Athonian-type fasting (AOF): Can significantly increase Omentin levels, which are known to decrease in obesity and type 2 diabetes .
Time-restricted eating (TRE): Shows effects on adipokine profiles including Omentin .
Energy restriction: Hypocaloric diets (1200-1500 kcal/day for women; 1500-1800 kcal/day for men) combined with time-restricted feeding windows demonstrate improvements in adipokine profiles .
These findings provide methodological guidance for researchers designing interventional studies targeting Omentin modulation.
Rat models have demonstrated particular utility in Omentin research:
Diet-induced obesity model: High-fat diet (60% fat, 21% carbohydrate, 18% protein, 5.1 calories/g) for 10 weeks successfully induces obesity and decreases Omentin levels, mimicking human pathophysiology .
Intervention protocol: Daily intraperitoneal injections of Omentin-1 (0.2 ml) for 14 consecutive days has shown efficacy in reversing metabolic alterations .
Control considerations: Vehicle-treated control groups receiving equivalent volumes of physiologic saline provide appropriate comparisons .
When designing animal experiments, researchers should include comprehensive metabolic assessments including glucose, insulin, lipid parameters, and tissue-specific analyses to fully characterize Omentin's effects.
The following validated protocols assess bone-related outcomes in Omentin research:
Macroscopic assessment: Examination of femur, tibia, and fibula morphology .
Quantitative measurements: Dry and ash weight of femur as indicators of bone mineralization .
Histological analysis: Longitudinal bone sections assess:
Molecular analysis: Gene expression studies of bone metabolism regulators using RT-PCR with primers:
These methodologies provide a comprehensive approach to characterizing Omentin's effects on bone metabolism.
Based on established methodologies in Omentin studies:
Data distribution analysis:
Comparative analyses:
Longitudinal data:
Significance thresholds:
Research demonstrates significant effects of Omentin on bone health:
High-fat diet-induced obesity leads to significant bone loss in rat models, with decreased dry and ash weight of femur .
Omentin-1 treatment antagonizes this bone loss, with significantly higher dry and ash weight of femur in treated versus untreated obese rats .
Histological examination reveals that Omentin-1 treatment prevents:
These findings suggest potential therapeutic applications for Omentin in preventing obesity-associated bone disorders through mechanisms potentially involving mTORC1 and AMPK signaling pathways.
While the search results don't provide detailed information on inflammatory pathways, several inferences can be made:
Omentin exists within a network of over 600 cytokines (adipokines) produced by adipose tissue that are involved in various metabolic processes including inflammation .
Its inverse relationship with obesity and related disorders suggests potential anti-inflammatory properties, as these conditions are characterized by chronic low-grade inflammation .
Dietary interventions that increase Omentin (such as Athonian fasting) also reduce vaspin, an adipokine that increases in obesity and type 2 diabetes .
These relationships warrant further investigation into Omentin's potential anti-inflammatory mechanisms through carefully designed molecular signaling studies.
Based on current evidence, several promising research directions emerge:
Therapeutic potential in metabolic disorders:
Developing recombinant Omentin as a potential therapeutic agent
Identifying dietary or pharmacological approaches to enhance endogenous Omentin production
Investigating Omentin's effects on insulin signaling pathways
Bone metabolism applications:
Characterizing molecular mechanisms underlying Omentin's bone-protective effects
Assessing potential applications in osteoporosis and other bone disorders
Investigating interactions with established bone metabolism regulators
Cardiovascular applications:
Evaluating Omentin's effects on endothelial function and atherosclerosis
Investigating potential cardioprotective mechanisms
Methodological advances:
Developing standardized assays for Omentin measurement
Establishing reference ranges across different populations
Creating tissue-specific conditional knockout models
Several methodological considerations impact Omentin measurement:
Preanalytical variables:
Fasting status of subjects
Time of day for sample collection (potential circadian variation)
Sample processing time and temperature
Storage conditions and freeze-thaw cycles
Analytical variables:
Antibody specificity and cross-reactivity
Assay sensitivity and dynamic range
Calibration standards and quality controls
Inter-laboratory variability
Biological variables:
Age and sex of subjects
BMI and body composition
Metabolic health status
Concurrent medications
Researchers should standardize these variables and include appropriate controls to enhance measurement reliability and cross-study comparisons.
When faced with contradictory findings regarding Omentin, researchers should:
Evaluate methodological differences:
Sample collection methods
Assay techniques
Sample processing and storage conditions
Consider study population heterogeneity:
Age and sex distributions
Metabolic health status
Comorbid conditions
Apply appropriate statistical approaches:
Meta-analysis of multiple studies
Sensitivity analyses to identify sources of heterogeneity
Subgroup analyses to identify population-specific effects
Examine contextual factors:
Dietary patterns of study participants
Physical activity levels
Medication use that might influence adipokine levels
Ethical research practices in Omentin studies include:
Human studies:
Animal studies:
Following guidelines from the Institute of Laboratory Animal Resources
Obtaining approval from institutional animal care and use committees
Using appropriate numbers of animals with power calculations
Providing proper housing conditions (comfortable temperature, regular light/dark cycles, adequate space)
Data reporting:
Transparent reporting of methodology
Publication of negative results
Sharing of raw data when appropriate
These ethical principles ensure research integrity while maximizing scientific value and minimizing harm.
Omentin is a single, non-glycosylated polypeptide chain consisting of 298 amino acids, with a molecular mass of approximately 33.2 kDa . The protein is produced in Escherichia coli (E. coli) and is purified using proprietary chromatographic techniques . The amino acid sequence of Omentin includes regions that are crucial for its biological activity, such as the ability to increase insulin-stimulated glucose uptake .
Omentin is predominantly expressed in visceral adipose tissue rather than subcutaneous adipose tissue . It is found in the stromal vascular cells within the adipose tissue, rather than in the adipocytes themselves . This localization is significant because visceral fat is closely associated with metabolic diseases such as diabetes and cardiovascular diseases.
One of the key functions of Omentin is its role in glucose metabolism. It has been shown to increase insulin-stimulated glucose uptake in adipocytes, which suggests that it may have an insulin-sensitizing effect . Additionally, Omentin has been observed to increase Akt phosphorylation, a process that is crucial for glucose uptake and metabolism .
The recombinant form of Omentin is produced in E. coli and is supplied as a sterile, filtered colorless solution . The protein is formulated in a buffer containing 20mM Tris-HCL (pH 8), 0.4M Urea, and 10% Glycerol . For optimal stability, it is recommended to store the protein at 4°C if used within 2-4 weeks, or at -20°C for longer periods. Adding a carrier protein, such as 0.1% HSA or BSA, can further enhance its stability .
Omentin’s role in glucose metabolism and its potential insulin-sensitizing effects make it a promising target for research into metabolic disorders such as diabetes and obesity . Differences in Omentin expression have also been noted in patients with inflammatory bowel disease, although the significance of these findings is still under investigation .