Herbal Remedies and Their Possible Effect on the GABAergic System and Sleep.
Study Design
- अध्ययन प्रकार
- Systematic Review
- हस्तक्षेप
- Herbal Remedies and Their Possible Effect on the GABAergic System and Sleep.
- तुलनित्र
- Placebo
- प्रभाव की दिशा
- Positive
- पूर्वाग्रह का जोखिम
- Unclear
Abstract
Sleep is an essential component of physical and emotional well-being, and lack, or disruption, of sleep due to insomnia is a highly prevalent problem. The interest in complementary and alternative medicines for treating or preventing insomnia has increased recently. Centuries-old herbal treatments, popular for their safety and effectiveness, include valerian, passionflower, lemon balm, lavender, and Californian poppy. These herbal medicines have been shown to reduce sleep latency and increase subjective and objective measures of sleep quality. Research into their molecular components revealed that their sedative and sleep-promoting properties rely on interactions with various neurotransmitter systems in the brain. Gamma-aminobutyric acid (GABA) is an inhibitory neurotransmitter that plays a major role in controlling different vigilance states. GABA receptors are the targets of many pharmacological treatments for insomnia, such as benzodiazepines. Here, we perform a systematic analysis of studies assessing the mechanisms of action of various herbal medicines on different subtypes of GABA receptors in the context of sleep control. Currently available evidence suggests that herbal extracts may exert some of their hypnotic and anxiolytic activity through interacting with GABA receptors and modulating GABAergic signaling in the brain, but their mechanism of action in the treatment of insomnia is not completely understood.
Full Text
Figures
Tables
Table 1
| Latin and Common Name | Known Chemical Components | Known Effect on Sleep | Target | Model | References |
|---|---|---|---|---|---|
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| Alkaloids, terpenes, organic acids and their derivatives, valepotriates, and flavones | Reduces sleep latency, improves subjective measures | GABAA receptor | In vitro studies; clinical studies | [ | |
| Magnolol and honokiol | Promotes REM sleep | GABAA receptor | In vitro studies; i.p. administration in mice | [ | |
| Schizandrin B | Promotes sleep | GABAA receptor | i.p. administration in mice and male rats | [ | |
| Benzodiazepines | Reduces sleep latency | GABAA receptor | In vitro studies; i.p. administration in male mice | [ | |
| Nuciferine, alkaloids | Promotes sleep | GABAA receptor | In vitro studies | [ | |
| Oleic acid, β-Sitosterol, and Stigmasterol | Increases sleep quality | GABAA receptor | p.o. administration in male mice | [ | |
| Kavapyrones | Decreases sleep latency; no effect on NREM sleep | GABAA receptor (not benzodiazepine site) | p.o. administration in mice | [ | |
| Sanjoinine A, suanzaorentang | Improves sleep quality, prolonging sleep time and increasing NREM sleep | GABAA receptor; activation of GABA synthesis through enhanced expression of GAD; serotonin receptors | i.p. and p.o. administration in male rats | [ | |
| Apigenin, alkaloids, flavones | Reduces sleep latency, increases sleep duration | GABAA and GABAB receptors, (and possibly GABAC receptor) | In vitro studies; p.o. administration in mice | [ | |
| Withanolide A, withaferin A | Reduces sleep latency, improves sleep quality | GABAA and GABAC receptors | In vitro studies; clinical studies | [ | |
| Alkaloids | Improves sleep latency and duration | GABAA receptor; serotonin receptor | In vitro studies | [ | |
| Tenufolin | Increases sleep duration | Increases the levels of GABA and GABA transporter 1 | Zebrafish and rats | [ | |
| Rosmarinic acid | Improves sleep quality | Decreases the level of GABA transaminase | In vitro studies; i.p. administration in mice | [ | |
| Ginkgotoxin, flavonoids, terpenoids | Improves subjective sleep quality measures | Inhibition of GAD activity | Clinical studies | [ | |
| Hypericin, pseudohypericin, hyperoside, among others | Increases REM latency and deep sleep | Inhibition of GAD and GABA transporter activity | Clinical studies | [ | |
| Limonene, β-myrcene | Increases sleep duration | Serotonergic system; proposed interaction with GABA receptor binders, such as diazepam | p.o administration in male mice | [ | |
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| Yokukansan | Various | Decreases sleep latency, improves dream content in the REM behavior disorder | GABAA receptor | p.o. administration in male mice; clinical studies | [ |
| Suanzaorentang, a traditional Chinese medicine | Various | Increases NREM, no effect on REM sleep | GABAA receptor; serotonergic system | Clinical studies | [ |
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