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Kava Root Extract

Kava Root Extract

Product Code: YSG-S-043
Used Part: Root
Active ingredient: Kavalactones
Specification: 10%-30%
Test Method: By HPLC
Appearance: Light yellow powder
Certifications: ISO, KOSHER, HACCP, HALAL...

PRODUCT INTRODUCTION

PRODUCT INTRODUCTION

Kava Root Extract Introduction

Kava root extract, which is also known as kava kava, is a plant from the South Pacific islands that belongs to the nightshade family. Pacific Islanders have involved it for many years as a stylized beverage to advance a condition of unwinding. Kava's calming and stress-relieving properties have recently garnered widespread attention.

The rhizomes of a perennial shrub in the South Pacific Islands yield kava root extract. Both the kava plant and its extracts are referred to as "kava," and it is typically consumed as a tablet or capsule containing either ethanolic or acetonic extracts. Kava's psychoactive kavapyrones, also known as kavalactones, are the plant's active ingredients.

 

 

 

Item No. Active Ingredients
YSG-S-043-10 Kavalactones ≥10.0%
YSG-S-043-20 Kavalactones ≥ 20.0%
YSG-S-043-30 Kavalactones ≥ 30.0%

kava root extract powder 002

kava root extract powder 001

Specification

Product Name Kava Root Extract Powder
Latin Name Piper Methysticum G.Forster.
Specification Kavalactones 10%--30%
CAS 9000-38-8
Appearance Light yellow powder
Bulk density 40-60g/100ml
Tapped density 60-90g/100ml
Particle size NLT 95% pass 80 mesh
Loss on drying ≤ 5.00%
Residue on Ignition ≤ 5.00%
Residual Solvent Ethanol<3000ppm
Total Heavy Metals ≤10ppm
Lead ≤3ppm
Arsenic ≤1ppm
Mercury ≤0.1ppm
Cadmium ≤1ppm
Pesticides residue ≤ 0.01mg/kg meet the requirement and its modifications
Total plate count ≤ 1000cfu/g
Yeast & Mould count ≤ 100cfu/g
Non-Irradiated, Non-GMO, Non-Allergen

Kava Root Extract Function

1) Disorders of Sleep

Kava root extract helped 24 people with insomnia caused by stress sleep better and less stressed. Kava extract was used to successfully treat sleep disturbances caused by anxiety, tension, and restlessness in 61 patients.

Kava blocks sodium and calcium ion channels, increases neurotransmitter binding to GABA-A receptors, inhibits monoamine oxidase B, and increases dopamine and noradrenaline, all of which could lead to sedative effects.

Although promising, there is insufficient evidence to support the use of kava in sleep disorders. To confirm these preliminary findings, additional clinical trials involving larger populations are required.

2) Sorrow

In a clinical preliminary on 60 individuals with summed up nervousness jumble, oral kava remove (250 mg kavalactones each day) decreased both tension and burdensome side effects. In a small study on 28 people with major depressive disorder, its combination with Saint John's wort improved depression but not anxiety or quality of life.

Mass kava extricate prompted a wonderful mental state while decreasing weakness and tension in human and creature studies. In cell models, kavalactones in kava decreased glutamate and slightly increased dopamine, serotonin, and GABA. Again, the outcomes look promising, but there have only been two brief clinical trials. To confirm the potential benefits of kava for people with depression, additional clinical research is required.

3) Menopausal Symptoms

Hot flashes, night sweats, insomnia, and increased anxiety and irritability are some of the perimenopausal and menopausal symptoms. In three clinical trials on 120 perimenopausal and menopausal women, kava root extract reduced anxiety, depression, irritability, and insomnia. It increased dopamine levels in the brain, inhibited monoamine oxidase-B, and activated GABA-A receptors.

Overall, there isn't enough evidence to say that kava helps with menopausal and perimenopausal mood symptoms. To confirm these findings, larger, more robust clinical trials are required.

4) Brain Function

In a small study on 20 people, a single dose of 300 mg of kava extract increased accuracy and performance on attention, visual processing, and working memory tasks. Kava kava root extract (200 mg, 3x/day) slightly improved word recognition performance in another study on 12 people.

The hippocampus, amygdala, and caudate nucleus of the brain are all areas of the brain where kava pyrones are in action. However, excessive use and prolonged use of kava can impair motor function. There is insufficient evidence to support the use of kava as a cognitive enhancer due to only two very small clinical trials. Clinical research needs to continue.

5) Drug Addiction Treatment

In a pilot study, cravings for addictive drugs were reduced in drug-dependent patients by using bulk kava extract. Dopamine-producing neurons in the reward system of the brain (nucleus accumbens) are the source of kava's anti-craving effects. Desmethoxyyangonin, a kava pyrone, may raise dopamine levels. We were unable to access a single pilot study for a critical analysis, so it is obvious that there is insufficient evidence to support the potential benefits of kava in the treatment of drug addiction. There is a need for more clinical research.

6. Animal and Cell Research

(Lack of Evidence) There is no clinical evidence that kava can be used to treat any of the conditions listed in this section. The current animal and cell-based research is summarized below, which should serve as a guide for future investigations. Nonetheless, the investigations ought not be deciphered as steady of any medical advantage.

Kava Root Extract Application

1.Health field:

Kava Root Extract can calm and relieve anxiety by reducing the excessive discharge of brain neurons.

2.Medical field:

Kava extract is often used as a raw material to be made into antibacterial and analgesic drugs.

 

★ Certificate:

All the ingredients are natural and approved BY ISO, KOSHER, HALAL, SC, HACCP approved.

YSG Certificates

★ The Best Kava Kava PowderSupplier:

Pls kindly to note that YSG current extraction process is water extraction and alcohol precipitation, all quality indicators are in line with the standards, including Pesticides ≤0,01 mg/kg fixed in the European regulation 396/2005, Benzo(a)pyrene≤10μg/kg and PAH(4) ≤50μg/kg fixed in the European regulation 1881/2006, etc. At the same time, the cargo will be sent to third-party laboratories for testing, such as Eurofins, SGS.

YSG

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