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- Aloe Vera (Aloe vera, Xanthorrhoeaceae)
- Biactivity
- Clinical Efficacy
- Systematic Review
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Date:
02-29-2016 | HC# 081513-539
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Re: Systematic Review of the Bioactive Components and Clinical Effects of Aloe Vera Gel
Radha MH, Laxmipriya NP. Evaluation of biological
properties and clinical effectiveness of Aloe
vera: A systematic review. J Tradit
Complement Med. 2015;5(1):21-26.
Aloe
vera (Aloe vera, Xanthorrhoeaceae)
is a succulent plant that has been used in traditional medicine for over 2000
years. Many of the biological effects of aloe vera have been associated with
the phytochemicals found in the leaf pulp (clear gel found in the inner leaves).
Although the pulp contains mostly water, other components include vitamins,
minerals, polysaccharides, and secondary metabolites. In this systematic review,
the bioactive components of aloe vera gel and their clinical effects were
evaluated.
Wound healing and immunomodulatory
effects
Aloe
vera gel has been reported to have healing effects on burn wounds. These
effects have been attributed to mannose-6-phosphate, a compound that increases
wound contraction and collagen synthesis, and to polysaccharides that have been
shown to affect the healing process. In a clinical study, the gel healed wounds
earlier than a standard treatment (1% silver sulfadiazine cream). Aloe vera gel
has also been reported to have immunomodulatory effects. In particular, it has
been shown to reduce inflammatory markers when inflammation is induced in human
cells and in rats (following burn injury). Clinical studies also showed that it
decreased wound size and the healing period in patients with canker sores, and
reduced inflammation in patients with inflammatory bowel disease. Some of these
immunomodulatory effects are attributed to constituent polysaccharides,
anthraquinones, and chromone.
Intestinal
absorption, antidiabetic effects, and antioxidant activities
Fermented
aloe vera gel exhibited probiotic effects by inhibiting the growth of
pathogenic bacteria without harming healthy gut bacteria. The laxative effects
of the gel are attributed to the compound aloin. There are five phytosterols
identified in the gel that were found to reduce visceral fat accumulation,
alter glucose metabolism, and reduce the size of intestinal polyps. The gel was
also reported to enhance intestinal drug transport, as well as to have
antihyperglycemic and antihypercholesterolemic activities without toxic
effects, in patients with type 2 diabetes. These actions may be due in part to
the anthraquinone, aloe-emodin-8-O-glycoside,
and phytosterols. Some of the antidiabetic and cardioprotective effects of aloe
vera gel may be due to antioxidant activity, improved carbohydrate metabolism,
and anti-inflammatory responses. Some of the antioxidant effects of the gel are
attributed to vitamins E and C, phenolic compounds, and polysaccharides. The
more important induction of phase II drug-metabolizing enzymes in reducing
oxidative stress should also be noted.
Hepatoprotective,
cytoprotective, and anticancer effects
Phytosterols,
isolated from aloe vera, upregulated the breakdown of fatty acids in the liver.
Aloe vera gel extract prevented ethanol-induced fatty liver (steatosis) by
suppressing lipogenic gene expression. The anti-inflammatory activity of aloe
vera may also explain its hepatoprotective effects. Many of the anticancer
effects of aloe vera gel are attributed to anthraquinones (aloin and aloe-emodin).
Aloin has chemoprotective effects and has prevented angiogenic responses in
human endothelial cells. Anthraquinones from aloe vera gel also suppressed
breast cancer proliferation by targeting estrogen
receptor-α protein stability. Estrogenic effects of aloe vera may also be effective
for conditions such as polycystic ovary syndrome (PCOS). Other studies suggest
that anthraquinones from aloe vera may also have neuroprotective effects.
Antimicrobial and
antiulcer effects
Aloe
vera gel has been shown to have antibacterial, antifungal, and antiviral
activities. Many of these reported effects are attributed to anthraquinones,
which are structural analogs of the antibiotic tetracycline (a drug that
inhibits bacterial protein synthesis). The antimicrobial effects of aloe vera
gel polysaccharides may involve the stimulation of phagocytic cells that
destroy bacteria. Phenolic compounds and a 14 kDa protein from aloe vera also are
reported to have antimicrobial effects. Aloe vera gel also has antimicrobial
and cytoprotective effects that may be especially effective for the treatment
of ulcers. Studies have also demonstrated that the gel improves the immune
response (in patients with human immunodeficiency virus [HIV]) and prevents
virus absorption, attachment, and entry into the cell. Anthraquinones from the gel
have also been found to inhibit the replication of viruses and induce
expression of interferon alpha-2, a cytokine that stimulates antiviral
responses in the body.
Antihyperlipidemic
effects
Several
clinical trials have demonstrated that aloe vera gel reduces total cholesterol and low-density lipoprotein (LDL)
cholesterol, and increases high-density lipoprotein (HDL) cholesterol. Other research
suggests that the gel may not only be effective for the management of PCOS, but
it also manages metabolic complications (e.g., hyperlipidemia) associated with
this condition. Phytosterols may contribute to some of the antihyperlipidemic
effects of aloe vera gel.
Despite the numerous clinical studies
and reported biological effects of aloe vera gel, there are still some concerns
about adverse effects. Although this review did not elaborate on the adverse
effects reported in human studies, the authors point out that animal studies
suggest potential cancer risk, sperm damage, and hematological and central
nervous system effects. Adverse
events have been linked to non-decolorized aloe (carbon filtration) that is
high in latex-derived anthraquinones. Toxicological studies on aloe treated to
reduce or remove anthraquinones have demonstrated safety. The topical use of
aloe vera appears to be safe, and some of the promising internal uses should be
further evaluated for efficacy and safety.
—Laura M. Bystrom, PhD
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