10.12.2012 Views

Encyclopedia of

Encyclopedia of

Encyclopedia of

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Ginger (Zingiber <strong>of</strong>ficinale) 245<br />

the knee as diagnosed by the American College <strong>of</strong><br />

Rheumatology classification criteria. [35] The primary<br />

efficacy variable was the proportion <strong>of</strong> responders<br />

experiencing a reduction in ‘‘knee pain on standing,’’<br />

using an intent-to-treat analysis. A responder was<br />

defined by a reduction in pain <strong>of</strong> 15 mm on a visual<br />

analog scale. During the 6-week treatment period,<br />

patients ingested 1 capsule twice daily <strong>of</strong> 255 mg<br />

ginger extract (EV.EXT 77, extracted from 2500–<br />

4000 mg <strong>of</strong> dried ginger rhizomes and 500–1500 mg<br />

<strong>of</strong> dried galanga rhizomes) or placebo. The percentage<br />

<strong>of</strong> responders experiencing a reduction in knee pain<br />

on standing was superior in the ginger extract group<br />

compared with the control group (63% vs. 50%;<br />

p ¼ 0.048). Analysis <strong>of</strong> the secondary efficacy variables<br />

revealed a consistently greater response in the<br />

ginger extract group compared with the control<br />

group, when analyzing mean values: reduction in<br />

knee pain on standing (24.5 vs. 16.4 mm; p ¼ 0.005)<br />

and reduction in knee pain after walking 50 ft (15.1<br />

vs. 8.7 mm; p ¼ 0.016). One group <strong>of</strong> adverse events<br />

showed a significant difference between treatment<br />

groups: Gastrointestinal (GI) adverse events were<br />

more common in the ginger extract group [116 events<br />

in 59 patients (45%)] compared with the placebo<br />

group [28 events in 21 patients (16%)]. None <strong>of</strong> the<br />

GI adverse events were considered serious by the<br />

investigators.<br />

Both <strong>of</strong> these studies suggest the strong need for<br />

dose escalation studies that can determine the most<br />

efficacious dose that it is still safe and well tolerated.<br />

Studies <strong>of</strong> longer duration are also required before<br />

more definitive conclusions can be drawn about the<br />

safety, tolerance, and effectiveness <strong>of</strong> ginger for<br />

osteoarthritis.<br />

Cardiovascular Effects<br />

In vitro research has shown that constituents in ginger<br />

have an inhibitory effect upon cholesterol biosynthesis.<br />

[36] Animal studies have demonstrated lipidlowering<br />

activity via enhancement <strong>of</strong> the activity <strong>of</strong><br />

hepatic cholesterol-7a-hydroxylase, the rate-limiting<br />

enzyme in bile acid biosynthesis, thereby stimulating<br />

conversion <strong>of</strong> cholesterol to bile acids, an important<br />

mechanism for eliminating cholesterol from the<br />

body. [37] A study in rabbits found that an orally administered<br />

ethanolic extract <strong>of</strong> ginger (200 mg=kg) reduced<br />

lipids after 10 weeks feeding <strong>of</strong> a cholesterol rich<br />

diet. The authors found that, at this dose, ginger<br />

produced results similar to those <strong>of</strong> gemfrimbrozil. [38]<br />

In contrast to the in vitro and animal data, a study <strong>of</strong><br />

patients with coronary artery disease found that 3 mo<br />

ingestion <strong>of</strong> 4 g=day dried ginger powder failed to<br />

lower blood lipids. [39]<br />

Ginger inhibits platelet aggregation in vitro, acting<br />

as a potent inhibitor <strong>of</strong> arachidonic acid, epinephrine,<br />

adenosine diphosphate (ADP), and collagen. A<br />

placebo-controlled study <strong>of</strong> 8 healthy males found<br />

that ingestion <strong>of</strong> 2 g <strong>of</strong> ginger caused a dose-dependent<br />

reduction <strong>of</strong> thromboxane synthetase and prostaglandin<br />

synthetase; however, no differences were<br />

found in bleeding time, platelet count, or platelet<br />

function between the placebo and control groups. [40]<br />

In patients with coronary artery disease (CAD),<br />

powdered ginger administered in a dose <strong>of</strong> 4 g=day<br />

for 3 mo did not affect ADP- and epinephrine-induced<br />

platelet aggregation. However, a single dose <strong>of</strong> 10 g<br />

produced a significant reduction in platelet aggregation<br />

induced by the two agonists. [39]<br />

Gastrointestinal Effects<br />

Ginger has long been valued in traditional medicine<br />

for a wide variety <strong>of</strong> gastrointestinal complaints.<br />

Researchers are beginning to explore possible scientific<br />

explanations for these historical uses. In vitro research<br />

indicates that constituents present in ginger have<br />

antiulcer activity. [41] Animal research demonstrates<br />

that ginger reduces the occurrence <strong>of</strong> gastric ulcers<br />

induced by nonsteroidal anti-inflammatory drugs<br />

(NSAIDs) and hypothermic restraint stress. [42] Cholagogic<br />

activity has been documented in rats with the<br />

acetone extract <strong>of</strong> ginger. [43]<br />

Helicobacter pylori (HP) is the primary etiological<br />

agent associated with dyspepsia, peptic ulcer disease,<br />

and development <strong>of</strong> gastric cancer. Novel, inexpensive,<br />

and safe approaches to the eradication <strong>of</strong> H. pylori<br />

are currently being sought. A methanol extract <strong>of</strong><br />

the dried, powdered ginger rhizome, fractions <strong>of</strong> the<br />

extract, and the isolated constituents, 6-, 8-, and 10gingerol<br />

and 6-shogaol, were tested against 19 strains<br />

<strong>of</strong> HP. [44] The extract inhibited the growth <strong>of</strong> all 19<br />

strains in vitro with a minimum inhibitory concentration<br />

(MIC) range <strong>of</strong> 6.25–50 mg=ml. One fraction <strong>of</strong><br />

the crude extract, containing the gingerols, was active<br />

and inhibited the growth <strong>of</strong> all HP strains with a<br />

MIC range <strong>of</strong> 0.78–12.5 mg=ml.<br />

DOSE<br />

As with many botanicals, dosage ranges vary widely<br />

in research and, especially, in the marketplace. The<br />

following are a few doses (serving sizes) found in the<br />

literature:<br />

Fresh or dried rhizome: 2–4 g daily. [45]<br />

Fluidextract: 1 : 1(g=ml) 0.25–1.0 ml 3 times daily;<br />

tincture 1 : 5(g=ml) 1.25–5.0 ml 3 times daily. [45]<br />

G

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!