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Fennel seeds extract prevents fructose-induced cardiac dysfunction in a rat model of metabolic syndrome via targeting abdominal obesity, hyperuricemia and NF-κβ inflammatory pathway.

Tissue & cell
June 1, 2024
Azza Mohamad El-Wakf et al. (8 authors)
Journal ArticleAnimal Study
Study Details

Study Goal

The researchers aimed to investigate whether fennel seeds extract (FSE) could prevent cardiac dysfunction in rats with metabolic syndrome induced by a fructose-enriched diet.

Results Summary

FSE effectively alleviated fructose-induced hypertension, ECG abnormalities, cardiac hypertrophy, metabolic alterations, oxidative stress, inflammation, and histological damage in rats. The study suggests FSE may serve as a complementary supplement for preventing metabolic syndrome-related cardiac issues.

Population

Adult male Wistar rats (160-170 g) with fructose-induced metabolic syndrome.

Effective Dosage

200 mg/kg body weight.

Duration

3 months.

Interactions

None mentioned.

Extracted Claims (23)
InterventionDirectionEndpointPopulationDosageImpactClaim #
fennel seeds extract (FSE) (200 mg/kg BW)
decrease
fructose-induced hypertension
fructose fed rats
-
showed high ability to alleviate
#1
fennel seeds extract (FSE) (200 mg/kg BW)
decrease
ECG abnormalities
fructose fed rats
-
showed high ability to alleviate
#2
fennel seeds extract (FSE) (200 mg/kg BW)
decrease
cardiac hypertrophy
fructose fed rats
-
showed high ability to alleviate
#3
fennel seeds extract (FSE) (200 mg/kg BW)
decrease
metabolic alterations
fructose fed rats
-
showed high ability to alleviate
#4
fennel seeds extract (FSE) (200 mg/kg BW)
decrease
oxidative stress
fructose fed rats
-
showed high ability to alleviate
#5
fennel seeds extract (FSE) (200 mg/kg BW)
decrease
inflammation
fructose fed rats
-
showed high ability to alleviate
#6
fennel seeds extract (FSE) (200 mg/kg BW)
decrease
histological injury
fructose fed rats
-
showed high ability to alleviate
#7
fructose (60%) enriched diet
increase
hypertension
rats
-
exhibited
#8
fructose (60%) enriched diet
increase
abnormal ECG
rats
-
exhibited
#9
fructose (60%) enriched diet
increase
heart rate
rats
elevated
exhibited
#10
fructose (60%) enriched diet
increase
serum glucose
rats
elevated
exhibited
#11
fructose (60%) enriched diet
increase
insulin
rats
elevated
exhibited
#12
fructose (60%) enriched diet
increase
lipids
rats
elevated
exhibited
#13
fructose (60%) enriched diet
increase
insulin resistance
rats
-
exhibited
#14
fructose (60%) enriched diet
increase
abdominal obesity
rats
-
exhibited
#15
fructose (60%) enriched diet
increase
cardiac hypertrophy
rats
-
exhibited
#16
fructose (60%) enriched diet
increase
hyperuricemia
rats
-
exhibited
#17
fructose (60%) enriched diet
decrease
cardiac antioxidants (GSH, SOD, CAT)
rats
-
showed significant reduction in
#18
fructose (60%) enriched diet
increase
oxidative stress indices (NADPH oxidase, O2.-, H2O2, MDA, PCO)
rats
-
showed elevation in
#19
fructose (60%) enriched diet
increase
NF-κβ
rats
-
showed elevation in
#20
fructose (60%) enriched diet
increase
pro-inflammatory cytokines (TNF-α, IL-1β, IL-6)
rats
-
showed elevation in
#21
fructose (60%) enriched diet
increase
adhesion molecules (ICAM-1, VCAM-1)
rats
-
showed elevation in
#22
fructose (60%) enriched diet
increase
serum cardiac biomarkers (AST, LDH, CK-MB, cTn-I)
rats
-
showed elevation in
#23
Abstract

BACKGROUND: Metabolic syndrome (MetS) is commonly associated with increased risk of cardiac disease that affects a large number of world populations. OBJECTIVE: This research attempted to investigate the efficacy of fennel seeds extract (FSE) in preventing development of cardiac dysfunction in rats on fructose enriched diet for 3 months, as a model of MetS. MATERIALS & METHODS: Thirty adult Wistar male rats (160-170 g) were assigned into 5 groups including control, vehicle, FSE (200 mg/kg BW) and fructose (60%) fed rats with and without FSE. Following the last treatment, blood pressure, ECG and heart rate were measured. Next, blood and cardiac tissues were taken for biochemical and histological investigations. RESULTS: Feeding fructose exhibited characteristic features of MetS involving, hypertension, abnormal ECG, elevated heart rate, serum glucose, insulin, lipids and insulin resistance, accompanied by abdominal obesity, cardiac hypertrophy and hyperuricemia. Fructose fed rats also showed significant reduction in cardiac antioxidants (GSH, SOD, CAT) with elevation in oxidative stress indices (NADPH oxidase, O2.-, H2O2, MDA, PCO), NF-κβ, pro-inflammatory cytokines (TNF-α, IL-1β, IL-6), adhesion molecules (ICAM-1, VCAM-1) and serum cardiac biomarkers (AST, LDH, CK-MB, cTn-I). Histopathological changes evidenced by destruction of cardiac myofibrils, cytoplasmic vacuolization, and aggregation of inflammatory cells were also detected. Consumption of FSE showed high ability to alleviate fructose-induced hypertension, ECG abnormalities, cardiac hypertrophy, metabolic alterations, oxidative stress, inflammation and histological injury. CONCLUSION: Findings could suggest FSE as a complementary supplement for preventing MetS and associated cardiac outcomes. However, well controlled clinical studies are still needed.

Medical Subject Headings (MeSH)
AnimalsMetabolic SyndromeFructosePlant ExtractsMaleNF-kappa BSeedsRats, WistarRatsDisease Models, AnimalHyperuricemiaFoeniculumInflammationOxidative StressSignal Transduction
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality75/10
Citation Metrics
Total Citations1
Citations/Year1.0
Research Impact Scores
APT Score0.05
Weight Score1.25
Normalized Score0.69
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