diptico a4 endolive ok - natacnatac is the global leading developer and manufacturer of value-added...
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![Page 1: Diptico A4 Endolive OK - NatacNATAC is the global leading developer and manufacturer of value-added Mediterranean herbal extracts, with a focus on olive tree and grapevine-derived](https://reader034.vdocument.in/reader034/viewer/2022042712/5f8c2aa0efb13304e5395c1e/html5/thumbnails/1.jpg)
NATAC is the global leading developer and manufacturer of value-added Mediterranean herbal extracts, with a focus on olive tree and grapevine-derived ingredients, and tailor-made formulations used by our customers to excel in their markets with unique ingredients for nutraceutical, food, feed, pharmaceutical and cosmetic applications. NATAC’s high quality ingredients are scientifically supported and adapted to the individual needs of our customers. Headquartered in Madrid, with 3 international branches for a global commercial presence.
KOSHER
NATAC, LLC2825 E Cottonwood Pkwy, Ste 500
Salt Lake City | UT | 84121 | USAwww.natacusa.com
NATAC CHILEKm 125 Camino a Pargua
Puerto Montt | Chilewww.natac.cl
NATAC CENTRAL OFFICESC/ Electrónica 7 | 28923 Alcorcón
Madrid | Spain(+34)918276470 | www.natac.es
www.endolivebynatac.com
www.endolivebynatac.comTHESE STATMENTS HAVE NOT BEEN EVALUATED BY THE FOOD AND DRUG ADMINISTRATION.
THIS PRODUCT IS NOT BEEN INTENTED TO DIAGNOSE, TREAT, CURE, OR PREVENT ANY DISEASE.
Technical InformationSpecificationPatented olive fruit extract containing
— 15% Oleanolic acid — 0,5% Tyrosol
— 10% Maslinic acid — 0,5% β-Sitosterol
— 5% Hydroxytyrosol
PatentsEP3007687; US2016143930; CA2915164; CN105530922; JP2016521717; WO2014198842; EP2305783;
US8361518; NZ590649; MX2011000786; JP5512671; ES2332977;CA2731917; AU2009273171
Dosage 200 mg/day
Suggested galenic formSoftgel capsules formulated with virgin olive oil as carrier. 2 capsules per day
Olive Fruit ExtractStudies performed by NATAC indicate that ENDOLIVE:
ENDOLIVE fulfills EFSA´s claim on olive polyphenols:"Olive oil polyphenols contribute to the protection of blood lipids from oxidative stress"
Natural Cardiovascular Protection
— Lowers serum glucose
— Increases HDL
— Controls systolic blood pressure
— Improves cardiac function
Reduces cardiovascular risk
EndoliveNatural Cardiovascular Protection
Endolive
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Clinical Studies: ENDOLIVE´s efficacy in treating cardiovascular disease was verified in a randomized
controlled trial in human volunteers. The efficacy of ENDOLIVE was proven in conferring cardiovascular
protection by decreasing relevant cardiovascular risk factors.
ENDOLIVE was administered to 30 subjects at a dosage of 200mg per day (100 mg softgel capsules
twice daily) for 8 weeks. The most representative results are summarized below.
BLOOD PRESSURE, CARDIAC FUNCTION & HDL CHOLESTEROL
PharmacokineticsENDOLIVE´s pharmacokinetic profile has been defined in human volunteers. Its bioavailability has been
reported in terms of oleanolic acid and maslinic acid. Significant amounts of triterpenes were found in
healthy subjects when ENDOLIVE was administered acutely at a dosage of 200mg.
The Burden of Cardiovascular DiseaseCardiovascular disease (CVD) is a significant,
ever-growing worldwide problem. Globally, CVD
accounts for 31% of all deaths and, the 80% of
them occur in developing nations where CVD is
expected to be the major cause of mortality by
2020. Not only is it a prime cause of mortality, but
is also the leading reason for disability-adjusted
life years lost globally.
Cardiovascular Risks Factors: Behavioral risk factors
(unhealthy diet, physical inactivity, tobacco use
and harmful use of alcohol) may show up in
individuals as:
— High blood pressure.
— Elevated blood glucose.
— Elevated blood lipids.
— Overweight and obesity.
Proven Efficacy Preclinical Approach: Our preclinical studies prove ENDOLIVE´s potential cardiovascular benefits based on
the observed effects on hypertension, arterial function and remarkably improved cardiac function in
hypertensive rats.
Figure 4. Systolic blood pressure (SBP) (A), Serum glucose (B), Serum HDL-Cholesterol (C) and Cardiovascular risk score (Framingham Risk Score – 10 year risk prediction) (D) in Control and ENDOLIVE-treated subjects after 8 weeks of treatment. * p<0.05 vs Control.
References: Valero-Muñoz et al., Mol. Nutr. Food Res., 2014, Stewart et al., JRSM Cardiovasc Dis. 2017, WHO. Cardiovascular diseases (CVDs). 2016, Mahmood etal., The Lancet 2014, Wilson et al. Circulation 1998, Yusuf et al. The Lancet 2004.*Additional technical information available on request
Ole
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EndoliveNatural Cardiovascular Protection
Figure 1. Systolic blood pressure (SBP) in spontaneously hypertensive rats (SHR) and spontaneously hypertensive rats treated with ENDOLIVE (SHR+ENDOLIVE) after 8 weeks of treatment. * p<0.05 vs SHR
ENDOLIVE significantly lowers elevated systolic blood pressure in hypertensive rats. Hypertension is one of the major risk factors for cardiovascular disease. It generates functional and structural changes in the arterial wall and target organs (heart, kidney, brain).
ENDOLIVE reduces aortic Collagen I protein expression in hypertensive rats.The accumulation of collagen induces fibrosis which can lead to aortic wall stiffness and arterial dysfunction. It has been postulated as one of the most relevant vascular changes involved in the progression of hypertension.
ENDOLIVE improves cardiac function by decreasing elevated left ventricle end diastolic pressure in hypertensive rats.Not only vessels, but also heart is prime target for hypertensive damage. Uncontrolled hypertension accelerates the damage which results in eventual heart dysfunction.
Figure 2. Collagen I protein expression in spontaneously hypertensive rats (SHR) and spontaneouly hypertensive rats treated with ENDOLIVE (SHR+ENDOLIVE) after 8 weeks of treatment. * p<0.05 vs. SHR.
Figure 3. Left ventricle end diastolic pressure (LVEDP) in spontaneously hypertensive rats (SHR) and spontaneouly hypertensive rats treated with ENDOLIVE (SHR+ENDOLIVE) after 8 weeks of treatment. * p<0.05 vs SHR.
SBP
(mm
Hg
)
100
150
200
250
SHR ENDOLIVE40
60
80
100
120
2,0
3,0
4,0
5,0
SHR ENDOLIVE
Co
llag
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I re
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xpre
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n (%
)
SHR ENDOLIVE
LVED
P (m
m H
g)
1 ENDOLIVE lowered systolic blood pressure in hypertensive rats.
2 ENDOLIVE preserved arterial function in hypertensive rats.
3 ENDOLIVE improved cardiac function in hypertensive rats.
** *
A ENDOLIVE controlledhigh systolic blood pressure.
SBP
(mm
Hg
)
Glu
co
se (
µm o
l/L)
HD
L-C
hole
stg
ero
l(m
g/d
l)
Ca
rdio
vasc
ula
r ris
ksc
ore
(%
)
B
50
75
125
100
150
CONTROL ENDOLIVE40
60
100
80
120
CONTROL ENDOLIVE
ENDOLIVE lowered serumglucose.
C ENDOLIVE raised serumHDL-cholesterol.
D
38
40
42
44
46
CONTROL ENDOLIVE2
3
4
6
7
5
8
CONTROL ENDOLIVE
ENDOLIVE lowered cardiovascular risk score.
*
*
*