Aloe Ferox Medicinal Properties - Anti-inflammatory

Inflammation is a non-specific immune response by the body to any type of injury. It is characterized by redness, heat, swelling and pain. According to Clayton (1993) the steps in inflammation are:

1. vasodilation that reduces blood pressure and increases blood flow (causing
   redness and heat)
2. followed by swelling due to an excessive amount of tissue fluid and
3. pain.

Vázquez (1996) demonstrated the anti-inflammatory effect of aloe ferox gel. It inhibited prostaglandin E2 production from arachidonic acid. While Yagi (1982) showed that the glycoprotein of aloe gel cleaved the bonds of the bradykinin molecule reducing pain and inflammation. In a later study (Bautista 2004) the antibradykinin effect was associated with the inhibition of prostaglandin synthesis.

Inflammation is also involved in conditions such as arthritis. Rheumatoid arthritis closely resembles adjuvant arthritis in rats and was studied by Davis (1992). According to this experiment aloe was injected and decreased inflammation (50%) and stimulated fibroblast growth repair.

Hanley (1982) showed when rat paws were injected with Aloe ferox it decreased inflammation (48%) and inhibited the immune response (72%). A subsequent study (Davis 1985) showed that when Aloe ferox was applied topically in a hydrophilic cream it reduced inflammation (39%) and subsequent arthritis (45%).

It has also been found that aloe has analgesic properties that can be ascribed to the presence of salicylates, which has an aspirin like effect (Shelton 1991).

Aloe Ferox Medicinal Properties - Anti-inflammatory

Inflammation is a non-specific immune response by the body to any type of injury. It is characterized by redness, heat, swelling and pain. According to Clayton (1993) the steps in inflammation are:

1. vasodilation that reduces blood pressure and increases blood flow (causing
   redness and heat)
2. followed by swelling due to an excessive amount of tissue fluid and
3. pain.

Vázquez (1996) demonstrated the anti-inflammatory effect of aloe ferox gel. It inhibited prostaglandin E2 production from arachidonic acid. While Yagi (1982) showed that the glycoprotein of aloe gel cleaved the bonds of the bradykinin molecule reducing pain and inflammation. In a later study (Bautista 2004) the antibradykinin effect was associated with the inhibition of prostaglandin synthesis.

Inflammation is also involved in conditions such as arthritis. Rheumatoid arthritis closely resembles adjuvant arthritis in rats and was studied by Davis (1992). According to this experiment aloe was injected and decreased inflammation (50%) and stimulated fibroblast growth repair.

Hanley (1982) showed when rat paws were injected with Aloe ferox it decreased inflammation (48%) and inhibited the immune response (72%). A subsequent study (Davis 1985) showed that when Aloe ferox was applied topically in a hydrophilic cream it reduced inflammation (39%) and subsequent arthritis (45%).

It has also been found that aloe has analgesic properties that can be ascribed to the presence of salicylates, which has an aspirin like effect (Shelton 1991).

Aloe Ferox Medicinal Properties

The healing properties of aloe have been known for millennia. The use of aloe was discovered on a Mesopotamian clay tablet (ca. 2100 BC). Aloes were listed in the Ebers papyrus (ca. 1500 BC) as an established cathartic.

Legend has it that aloe was an important part of the beauty regimen of the Egyptian queens, Nefertiti and Cleopatra. The Greek physician Dioscorides, while accompanying Nero’s army, mentioned aloe in his writing (ca 100 AD). Alexander the Great (356–323 BC) was persuaded by Aristotle to capture the island of Socrota in the Indian Ocean to secure its aloe supplies to treat his wounded soldiers (Bruce 1975).

Numerous Aloe species have been used medicinally but only Aloe ferox, Aloe perryi and Aloe vera have demonstrated any commercial importance (Grindlay 1986). Scientific literature now documents various medical applications.

Aloe gel has demonstrated anti-inflammatory (Vázquez 1996, Bautista 2004), wound healing (Davis 1989, 1994, Heggers 1996), anti-tumour (Kim 1999, Pecere 2000), antiviral (McDaniels 1990a,b), anti-microbial (Wang 1998) and anti-diabetic (Reynolds 1999) activity.
It has also shown immune stimulating (Zhang 1996, Strickland 2001) and cholesterol lowering activity (Tizard 1989).

The active constituent in the aloe exudate (bitter) is the anthrones. They are degraded in the colon by bacteria to aloe-emodin, which function as a stimulant laxative (Blumenthal, 1998).

Studies have also demonstated aloe-emodin to be antiviral (Sydiskis 1991), an antioxidant (Yen, 2000), effective for liver cancer prevention (Kuo 2002) and inhibits neuroectodermal tumor cell growth (Pecere 2000).

Aloe Ferox Medicinal Properties

The healing properties of aloe have been known for millennia. The use of aloe was discovered on a Mesopotamian clay tablet (ca. 2100 BC). Aloes were listed in the Ebers papyrus (ca. 1500 BC) as an established cathartic.

Legend has it that aloe was an important part of the beauty regimen of the Egyptian queens, Nefertiti and Cleopatra. The Greek physician Dioscorides, while accompanying Nero’s army, mentioned aloe in his writing (ca 100 AD). Alexander the Great (356–323 BC) was persuaded by Aristotle to capture the island of Socrota in the Indian Ocean to secure its aloe supplies to treat his wounded soldiers (Bruce 1975).

Numerous Aloe species have been used medicinally but only Aloe ferox, Aloe perryi and Aloe vera have demonstrated any commercial importance (Grindlay 1986). Scientific literature now documents various medical applications.

Aloe gel has demonstrated anti-inflammatory (Vázquez 1996, Bautista 2004), wound healing (Davis 1989, 1994, Heggers 1996), anti-tumour (Kim 1999, Pecere 2000), antiviral (McDaniels 1990a,b), anti-microbial (Wang 1998) and anti-diabetic (Reynolds 1999) activity.
It has also shown immune stimulating (Zhang 1996, Strickland 2001) and cholesterol lowering activity (Tizard 1989).

The active constituent in the aloe exudate (bitter) is the anthrones. They are degraded in the colon by bacteria to aloe-emodin, which function as a stimulant laxative (Blumenthal, 1998).

Studies have also demonstated aloe-emodin to be antiviral (Sydiskis 1991), an antioxidant (Yen, 2000), effective for liver cancer prevention (Kuo 2002) and inhibits neuroectodermal tumor cell growth (Pecere 2000).

Links:

http://www.FeroxAloe.com/
http://www.Alofe.com/
http://aloeferox.webs.com/
http://aloeferox.talkspot.com/

Aloe Ferox introduction:

The Ferox Aloe plants used to make Ferox Aloe health products are robust plants. Ferox Aloe plants grow wild in their natural habitat and Ferox Aloe plants DO NOT require treatment with fertilizers, pesticides or fungicides which may impact on the quality of the final product. Ferox Aloe plants might be the most powerful plant known to man, the Ferox Aloe is definitely the strongest in the Aloe family.

Scientific tests carried out on Aloe ferox and Aloe vera plants, growing side by side at Kirstenbosch National Botanical Gardens, Cape Town, South Africa, showed that:

• After extraction, the juice of Aloe vera leaves decolourizes and loses viscosity much more rapidly than does the juice of Ferox Aloe. The gelly of Ferox Aloe does not require artificial stabiliza
• Juice expressed from the whole leaves of Ferox Aloe and Aloe vera were compared for their solid content by precipitation with acetone and centrifugation. Demonstrable solids in Ferox Aloe were consistently greater in volume than those obtained from Aloe vera.
• In comparison of unprocessed leaf juice, the amino-acid content of Ferox Aloe is at least three times greater than that of Aloe vera.