High Mountain Gaba Tea - Lu Shan 150g

High Mountain Gaba Tea - Lu Shan 150g

Finlandia Alchemy

  • $70.95
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The term ‘clouds & mist’ refers to blankets of nourishing mists that develop in the forests and valleys each day and provide a lush, moist environment for the forest, birds and tea gardens. Lu Shan is blessed with ample water from the Yangtze River and Lake Poyang. Rich hydration results in sweet, tender buds and leaves that are filled with abundant plant nutrient and sweetness. The deep green color of Lu Shan suggests this rich, unspoiled environment. The long, thin leaves speak to hand-processing skills that are second to none. This is an extremely well-made tea.

Lu Shan tea has a stunning aroma – it is full of vibrancy and spring life. If one has never tried a Chinese spring green tea before, this would be our recommendation of where to start.

Flavor: deep, rich, abundant sweetness

Aroma: pure, fresh, vegetal aroma of early spring plants

Liquor: clear amber-colored liquor tending towards a light moss green color

GABA tea is an all-natural source of GABA. It was discovered more than 20 years ago by Japanese researchers looking for a natural method to preserve food. They discovered that tea which is oxidized in a nitrogen-rich atmosphere has a higher concentration of GABA elements than any other type of tea. Oxidation refers to exposing tea leaves to the air after they have been picked. Black tea is 100% oxidized. Green tea is unoxidized - it is dried as soon as possible after picking. GABA tea production involves exposing fresh tea leaves to nitrogen instead of oxygen. The fresh tea is placed in stainless steel vacuum drums and the oxygen is removed and replaced with nitrogen. The tea leaves are exposed to this nitrogen-rich atmosphere for about 8 hours. The temperature must be kept above 40 degrees Celsius for the duration of the processing. This procedure produces the highest concentrations of natural GABA.

 

GABA- Gamma amino butyric acid

Gamma amino butyric acid (GABA) is one of the major inhibitory neurotransmitters in the central nervous system, balancing the excitatory effects of glutamate on neuronal activity. The inhibitory effects of GABA are generally considered to lessen anxiety, relax muscle tension, and have sedative-like effects. In addition, conditions such as anxiety, depression, insomnia, and epilepsy have all been associated with low GABA concentration or activity.

GABA has also been shown to cause a significant increase in alpha brain waves compared to control, indicative of a more relaxed state, as well as better concentration.

Increasing GABA activity is also a therapeutic target for many medications used in the treatment of insomnia, often by targeting GABA receptors. This has the effect of decreasing waking, shorten sleep latency, and increasing slow-wave sleep

References:

  1. Gajcy K, Lochyñski S, Librowski T. A role of GABA analogues in the treatment of neurological diseases. Curr Med Chem. 2010;17(22):2338-47.
  2. Kendell SF, Krystal JH, Sanacora G. GABA and glutamate systems as therapeutic targets in depression and mood disorders. Expert Opin Ther Targets. 2005:9:153-168.
  3. Nemeroff CB. The role of GABA in the pathophysiology and treatment of anxiety disorders. Psychopharmacol Bull. 2003:37:133-146.
  4. Abdou AM, Higashiguchi S, Horie K, et al. Relaxation and immunity enhancement effects of gamma aminobutyric acid (GABA) administration in humans. Biofactors 2006;26:201-208.
  5. Yoto A, Murao S, Motoki M, et al. Oral intake of -aminobutyric acid affects mood and activities of central nervous system during stressed condition induced by mental tasks. Amino Acids. 2012 Sep;43(3):1331-7. doi: 10.1007/s00726-011-1206-6.
  6. Yang Y, Koh D, Ng V, et al. Self perceived work related stress and the relation with salivary IgA and lysozyme among emergency department nurses. Occup Environ Med. 2002;59(12):836-841.
  7. Walsh JK, Salkeld L, Knowles LJ, et al. Treatment of elderly primary insomnia patients with EVT 201 improves sleep initiation, sleep maintenance, and daytime sleepiness. Sleep Med. 2010 Jan;11(1):23-30. doi: 10.1016/j.sleep.2009.07.012.

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