inflammation

Lion's Mane (Hericium erinaceus)

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What is Lion's Mane?

Lion's mane is a medicinal wood-rotting fungus with a characteristic growth pattern that resembles the shaggy mane of a lion.

The fungus prefers temperate forests in North America, Europe, and Asia where it thrives on living oak, beech, or conifer trees.

The medicinal benefit of lions mane primarily involve the nervous system. Modern applications use the mushroom for general cognitive health and as a natural nootropic substance.

This mushroom is also eaten as a delicacy — with a flavor similar to lobster when cooked with butter.

In recent years lion's mane has caught the eye of the nootropic community for its ability to up-regulate nerve growth factor.

Top Lion’s Mane Products

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Host Defense Lion’s Mane Capsules

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Host Defense Lion’s Mane Tincture

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Host Defense Stamets 7

 

How Is Lion's Mane Used?

Lion's mane is mainly used for neurodegenerative disorders like dementia and multiple sclerosis. It's also popular as a nootropic agent for supporting optimal cognitive function long term.

Most of the people using this fungus take it in the form of a powdered capsule or tincture on a daily basis. Like most medicinal mushrooms, the biggest benefit comes from using the herb on a regular basis over long periods of time — rather than short bursts for quick impact of effects.

 

Traditional Use of Lion’s Mane

Lion’s mane mushrooms have a long history of use in Eastern Asia — including China, Korea, and Japan. Each of these regions used the mushroom for treating neurological disorders, including neurasthenia, and age-related cognitive decline, as well as for general health.

 

Herb Details: Lion's Mane

Herbal Actions:

  • Antibacterial
  • Anticancer
  • Antidiabetic
  • Antioxidant
  • Cardioprotective
  • Hepatoprotective
  • Nervine
  • Immunomodulator

Weekly Dose

Part Used

  • Fruiting Body

Family Name

  • Hericiaceae

Distribution

  • North America, Europe, Russia, Mountainous regions of Asia

Constituents of Interest

  • Hericnones
  • Erinacines
  • Lactones
  • Polysaccharides

Common Names

  • Lion's Mane
  • Monkey's Head
  • Hedgehog Fungus
  • Pom Pom
  • Houtou (China)
  • Shishigashira (China)
  • Yamabushitake (Japan)

Pregnancy

  • Safe during pregnancy.

Duration of Use

  • Long term use acceptable and recommended.
 

Mycological Information

The Hericiaceae family of fungi are saprophytic (consumes dead wood), yet can be found growing on living trees as well. Many experts believe the mushroom has a mutualistic relationship with the tree for some time — helping it resist disease and infection, but will eventually consume the tree after it dies.

Hericium mushrooms normally grow in cooler, mountainous regions across the globe. It contains a number of species used medicinally and nutritionally.

Hericium spp. has characteristic "tooth" structures on its fruiting body, giving it a hair-like appearance.

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Pharmacology & Medical Research

+ Neuroprotective

Lion’s mane offers several different mechanisms to produce its overall neuroprotective benefits:

  1. Antioxidant and free-radical scavenging activity [6]
  2. Anti-inflammatory activity
  3. Nerve-growth factor stimulation (hericium and erinacenes)
  4. Reduction of endoplasmic reticulum stress-dependant cell death (dilinoleolyl-phosphatidylethanolamine (DLPE) [7]
  5. Attenuation of beta-amyloid-related cognitive decline in animals (dementia model) [8]
  6. Enhance mylenation of neurons [9, 10, 11]

In animal studies, lion’s mane has been shown to reduce the severity of damage after a stroke — effectively protecting the sensitive neurons from ischemic damage [6].

Clinical Trials:

Study: Mori et al., 2009 — Improving effects of the mushroom Yamabushitake (Hericium erinaceus) on mild cognitive impairment: a double‐blind placebo‐controlled clinical trial. [5]

This randomized, double-blind, placebo-controlled clinical trial involving 30 Japanese men and women with mil cognitive impairment found that after 16 weeks, the lion’s mane group had significantly increased cognitive scores. These improvements were noted as early as the 8 week checkup, and continued to improve compared to placebo over the rest of the 16-week trial.

The dose of lion’s mane used in this study was 1 gram of dried lion’s mane taken three times per day.

Unfortunately, 4 weeks after the trial concluded, the scores had significantly decreased — indicating that these effects are not permanent and the mushroom needs to be continued to remain effective.

+ Nootropic

A nootropic is a substance that improves cognition without causing harm. There are a lot of nootropic substances that range from herbs like lion’s mane or rhodiola, to synthetic or prescription drugs like Modafinil or Noopept.

Lion’s mane is thought to be a nootropic through its ability to promote nerve-growth factor (NGF) in the brain. NGF is the most potent growth factor for the cholinergic neurons. it influences everything from the proliferation, differentiation, and survival of neuronal cells in the brain [8, 12].

Reductions in NGF has been considered a major implication in conditions such as depression, substance abuse, Alzheimer’s disease, and Huntington’s disease [12].

There have been a lot of studies looking at the role of lion’s mane and nerve growth factor — most of which have concluded that lion’s mane applications directly lead to an increase in NGF. This research has been done both in vivo and in vitro [13, 14, 15, 16].

This effect is very important. We can give peptides like NGF to people to treat these neurodegeneration, but these peptides rarely cross the blood brain barrier [9]. Therefore, finding alternative ways to boost NGF or other peptides in the brain are of the utmost importance in the treatment, prevention, and management of neurodegenerative disorders.

+ Immunomodulation

Like many other medicinal mushrooms, lion’s mane contains a high concentration of polysaccharides with immunomodulatory effects.

A lot of this study has been done in vitro with dendritic immune cells. These cells serve as the antigen-presenting cells that act as central mediators for the immune response as a whole. They’re responsible for a lot of the tolerance formed by the immune system to help maintain homeostasis.

Studies involving lions mane extracts have shown the fungus can stimulate the maturation of dendritic cells, induce dendritic cell activation, and modulate key T-helper (Th1) immune responses [17].

+ Anti-Inflammatory

Lion’s mane has been shown to influence a variety of inflammatory mediators, including:

Induces IL-1β expression through Nf-kB, NF-IL6, and activator protein 1 (AP-1) [18]

Induces iNOS gene expression to increase nitric oxide (NO) production in macrophages

Inhibits toll-like receptor 4 (TLR4)-JNK signalling on macrophages [19]

 

Phytochemistry of Lion’s Mane Mushrooms

Lion’s mane fruiting body and myclelia contain an exceptionally diverse range of unique bioactive substances — including polysaccharides, meroterpenoids (hericinones), cyathane diterpenoids (erinacines), steroids, alkaloids, and lactones.

The most significant constituents in terms of the mushrooms medicinal action are the hericenones and erinacines. Both of these substances have been shown to stimulate nerve growth factor in the central nervous system. This is thought to be the primary mechanism for which the fungus an improve the health and function of the nervous system.

 

Clinical Applications Of Lion's Mane:

Lion's mane has many uses, but the most well-known is as a neuroprotective, and nootropic benefits. It's useful for neurodegenerative disorders including multipple sclerosis, Alzheimer's disease, and Parkinson's disease.

Other uses include depression and anxiety, cancer, diabetes, gastrointestinal infection, and fatigue.

 

Cautions & Safety

Lion’s mane is a culinary mushroom that’s been used for both food and medicine by countless individuals over several hundreds of years. There are no expected short-term or long-term side effects from using the fungus.

Throughout the clinical research there have been no reports of serious side effects from using the fungus — including very high-potency extracts and long-term durations of use.

Caution advised with any blood clotting conditions or medications due to possible agonistic interactions — including haemophilia or other bleeding disorder, thrombocytopenia, or post-surgery. Lion’s mane may interact with blood thinners or anti-platelet medications.

 

Author:

Justin Cooke, BHSc

The Sunlight Experiment

(Updated April 2020)

 
 

Recent Blog Posts:

References

Stevia (Stevia rebaudiana)

Stevia is used as a sugar alternative and antidiabetic. The source of stevias sweetness comes from special phytochemicals known as glycosides. They are up to 160 times sweeter...

Cannabis (Cannabis sativa/indica)

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Cannabis Overview

Cannabis is well known for its psychoactive effects, causing temporary changes in visual and auditory perception.

The cannabis plant is also a rich source of medicinal compounds. Cannabinoids related to THC exert medicinal action through the endocannabinoid system — a critical component of homeostasis.

Many of these cannabinoids aren't psychoactive, and wont produce the 'high' associated with the plant in their isolated forms.

Compounds like CBD, have become especially popular as a supplement recently for its broad medicinal benefits.

There are plenty of uses for cannabis — however, product selection, strain choice, and cannabinoid profiles make a big difference in the effects produced by the plant. It's important to use the right type of cannabis for the job.

 

What is Cannabis Used For?

Using cannabis as medicine poses challenges due to the large variety of effects each cannabinoid possesses. Different cannabinoid and terpene ratios can produce different effect profiles.

The plant has many claimed benefits, and though a lot of them can be validated, it's not a miracle plant.

Cannabis is especially reliable for a few key symptoms:

  • Lowering various forms of inflammation
  • Improving microbiome diversity (through CB2 receptor activity)
  • Reducing nervous excitability
  • Reducing convulsions
  • Improving sleep onset and maintenance
  • Lowering pain

Using cannabis as medicine should be attempted with caution due to the degree of variability the plant produces in terms of effect profile. What this means is that some cannabis extracts will make symptoms like anxiety worse, while others can dramatically improve it.

Choosing the right strain or extract is of the utmost importance when using cannabis as medicine.

The effects of cannabis can be contradictory:

  • It's both a stimulant and a sedative
  • It increases appetite, and suppresses it
  • It increases immune activity, and suppresses inflamamtion

These effects all contradict themselves in most cases. The reason this happens is because the cannabinoids work through a regulatory pathway (endocannabinoid system) rather than on a particular organ function.

It's similar to how adaptogens like ginseng, ashwagandha, or reishi produce often contradictory or bidirectional results.

+ Indications

  • Anorexia
  • Cancer
  • Crohn's disease
  • Dystonia
  • Epilepsy
  • General anxiety disorder
  • Glaucoma
  • Gout
  • Insomnia
  • Menstrual cramping
  • Multiple Sclerosis
  • Neuropathic pain
  • Osteoarthritis
  • Rheumatoid Arthritis
  • Schizophrenia (Caution)
  • Social anxiety disorder
  • Substance abuse/addiction
  • Ulcerative colitis

+ Contraindications

  • Only use cannabis medicinally following the direction of a qualified medical practitioner.
  • Caution with anxious or depression.
  • May worsen symptoms of psychosis
  • Avoid use alongside medications unless first discussing with your doctor.

+ Potential Side-Effects

  • Apathy (long-term use)
  • Bronchitis (smoking)
  • Cough (smoking)
  • Depression
  • Dizziness
  • Dry eyes
  • Dry mouth
  • Eye reddening
  • Fatigue
  • Hallucinations
  • Headache
  • Heart palpitations
  • Hypertension/Hypotension
  • Increased appetite
  • Lightheadedness
  • Menstrual changes
  • Nausea/vomiting
  • Numbness
  • Paranoia
  • Tachycardia
 

Herb Details: Cannabis

Weekly Dose

Part Used

  • Leaves, flowers, seeds

Family Name

  • Cannabacea

Distribution

  • Worldwide

Herbal Actions:

  • Sedative/Stimulant
  • Anti-emetic
  • Anti-spasmodic
  • Anti-convulsant
  • Analgesic
  • Antinflammatory
  • Appetite Suppressant/Stimulant
  • Adaptogen
  • Anti-cancer
  • Antioxidant

Common Names

  • Cannabis
  • Marijuana
  • Hemp
  • Mary Jane
  • Herb

Pregnancy

  • Avoid use while pregnant and nursing.

Duration of Use

  • Long-term use acceptable. Recommended to take breaks periodically.

CYP450

  • CYP2C9
  • CYP3A4
 

Botanical Information

Cannabis plants are members of the Cannabacea family. This small family comprises only 11 different genuses, and about 170 species.

Some common members of the family are hops (Humulus spp.) and celtis (Celtis spp.). The celtis genus contains the largest collection of species by far, with over 100 different species. Cannabis and Humulus are the closest related genus' in the group by far.

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There are three species of cannabis:

1. Cannabis sativa

Cannabis sativa is a tall, fibrous plant. It's high in cannabinoids, terpenes, and other phytochemicals — giving it many uses medicinally.

Cannabis sativa is the most commonly cultivated species. There are hundreds, if not thousands of different phenotypes of this species — the most important being hemp — which is a non-psychoactive, high fiber plant valued as both a health supplement and textile. It's also used for food (seeds), and to make biodeisel.

There are also Cannabis sativa strains high in the psychoactive component — THC — which make it popular as both medicine and recreational intoxicant.

2. Cannabis indica

Cannabis indica grows as s shorter, bushier plant. It's hgiher in THC, and there are few low-THC phenotypes available for this plant.

This species of cannabis is most often used recreationally.

3. Cannabis ruderalis

Cannabis ruderalis is a small, herbaceus plant more closely related to Cannabis sativa than Cannabis indica. It's low in cannabinoids, and terpenes, as well as fiber — limiting its value to humans.

This species has the unique ability to initiate flower production irrelevant to day length. Plant breeders have started mixing the plant with other species to gain these benefits. This makes cultivation easier in areas where day length is too short or too long for optimal cannabis cultivation.

 

Phytochemistry

There are 421 compounds in the cannabis plant [1], at least 66 of these are cannabinoids — some sources report as many as 112.

The top 6 cannabinoids in the plant (CBD, CBG, CNN, THC, THCV, and CBC), account for the vast majority of the cannabinoid profile.

The phenotype of the cannabis used is the primary determining factor for the cannabinoid profile of each plant.

Hemp plants for example, contain much higher levels of CBD, and lower levels of THC. Marijuana strains are the opposite, contianing high THC, and lower CBD.

Depending on the strain, this can vary dramatically — and you can find almost any combination of cannabinoid possible.

comparing-CBD-from-hemp-and-marijuana.jpg
 

The Cannabinoids:

Cannabinoids are a class of phytochemical compounds resembling the structure of our naturally occurring ecosanoid endocannabinoids; anandamide, and 2-AG. There are roughly 66 of these compounds in the cannabis plant, and a few found in other species of plants as well — such as helichrysum and echinacea.

Although the cannabinoids are very similar, their binding activity varies a lot [14]. Some bind to CB1 receptors (located primarily in the central nervous system), others bind to CB2 receptors (found primarily in immune tissue). Some cannabinoids will even bind to both, or work by increasing the concentrations of naturally occurring endocannabinoids instead.

Due to the wide range of variability between each cannabinoid, it’s useful to go over them in greater detail individually.

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CBC.jpg

1. CBC

Cannabichromene

CBC is the third most abundant cannabinoid in the cannabis plant.

It’s non-psychoactive.

CBC is far less studied than the two preceding cannabinoids CBD, and THC, though early research is starting to suggest it’s even better for treating conditions like anxiety than the famed CBD.

CBC content can be increased in the cannabis plant by inducing light-stress on the plant [5].

CBC Medicinal Actions

  • Antidepressant

  • Mild sedative

Receptors Affected

  • Vanilloid receptor agonist (TRPV3 and TRPV4) [4]

 
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CBD.jpg

2. CBD

Cannabidiol

In many cases, CBD is the most abundant cannabinoid. Only selectively bred cannabis strains will have higher THC concentrations than CBD.

CBD is famed for many reasons. It offers a wide range of medicinal benefits, and has been well-studied and validated over the past two decades.

CBD oils, e-liquids, and edibles have become highly popular in recent years as more of this research is being released and translated for the general public.

CBD Medicinal Actions

  • Antinflammatory

  • Mild appetite suppressant

  • Lowers stress

  • Adaptogenic

  • Mild sedative

  • Anti-emetic

Receptors Affected

  • Adenosine (A2a) reuptake inhibitor [6]

  • Vanilloid pain receptors (TRPV1, TRPV2, TRPV3) [7]

  • 5HT1A receptor agonist (serotonin receptor) [6]

  • FAAH (–) [6, 7]

  • PPARγ nuclear receptor (+) [48]

  • Mg2+‐ATPase (−) [11]

  • Arylalkylamine N‐acetyltransferase (−) [44]

  • Indoleamine‐2,3‐dioxygenase (−) [45]

  • 15‐lipoxygenase (−) [46]

  • Phospholipase A2 (+) [11]

  • Glutathione peroxidase (+) [47]

  • Glutathione reductase (+) [47]

  • 5‐lipoxygenase (−) [46]

Metabolism

  • CYP1A1 (−) [40]

  • CYP1A2 & CYP1B1 (−) [40]

  • CYP2B6 (−) [41]

  • CYP2D6 (−) [42]

  • CYP3A5 (−) [43]

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CBG.jpg

3. CBG

Cannabigerol

CBG is an early precursor for many of the other cannabinoids including THC.

Plants harvested early will be high in this compound.

Many users report that strains high in CBG are less likely to cause anxiety, and are good for people experiencing acute stress.

This is likely due to its role in blocking the serotonergic effects of THC through the 5-HT1A serotonin receptors [9].

CBG Medicinal Actions

  • Anti-anxiety

  • Adaptogenic

  • Mild sedative

Receptors Affected

  • A2-adrenoceptor antagonist [9]

  • CB1 and CB2 receptors agonist [9]

  • 5-HT1A receptors antagonist (serotonin receptor) [9]

  • Vanilloid receptor agonist (TRPA1) [8]

  • TRPM8 receptor antagonist [8]

 
cbn-cannabinol-header.jpg
CBN.jpg

4. CBN

Cannabinol

CBN is made from THC. As THC content breaks down with time, or heat, CBN levels increase overall.

Older harvested plants that have gone past their window of ripeness will be much higher in CBN.

It’s mostly non-psychoactive but may have some mild psychoactivity in some people.

Products or strains high in CBN will produce more of a heavy feeling and are best used for treating conditions like insomnia or anxiety.

This cannabinoid is potentially the most sedative of the group.

CBN Medicinal Actions

  • Sedative

  • Anti-anxiety

  • Appetite stimulant

Receptors Affected

  • CB1 receptor agonist [10].

Metabolism

  • CYP2C9

 
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THC.jpg

5. THC

Tetrahydrocannabinol

THC is the main psychoactive compound in the cannabis plant.

There are two main types:

  • Delta-8-THC — contained in very small amounts

  • Delta-9-THC — the most abundant form of THC in the cannabis plant

THC activates both CB1 and CB2 endocannabinoid receptors, causing changes in neurotransmitters like dopamine, norepinephrine, and most importantly, serotonin. It’s this change in neurotransmitter levels that produce the bulk of the high experienced by this compound.

Aside from its psychoactive effects, THC has medicinal benefits of its own.

It’s mentally stimulating and has some potent antidepressant effects through its euphoric effects.

THC Medicinal Actions

  • Appetite stimulant

  • Sedative (low doses)

  • Stimulant (high doses)

Receptors Affected

  • CB1 and CB2 agonist [11]

  • PPAR gamma receptor agonist [11, 15].

Metabolism

  • CYP2C9

 
thcv-Tetrahydrocannabivarin-header.jpg

6. THCV

Tetrahydrocannabivarin

THCV is the fraternal twin of THC.

It’s virtually identical except for one slight chemical difference — THCV is missing two carbon atoms.

This makes the effects of THCV very similar to THC — but is much weaker in its effects.

One study reported THCV as being 20-25% as strong as THC in its psychoactive effects [12].

There are others affected by this, including CBCV, and CBDV, though they are in far less concentrations.

tse-cannabinoid-family.jpg

THCV Medicinal Actions

  • Appetite suppressant

  • Euphoric

  • Antispasmodic

  • Paranoic

Receptors Affected

  • Vanilloid receptor agonist (TRPV3 and TRPV4) [13].

 
other-cannabinoids-header.jpg

7. Other Cannabinoids

There are also a lot of cannabinoids that can be found in much lower concentrations.

These make up the bottom 5% of the cannabinoid profile.

Few of these cannabinoids have many studies on them aside from chemical mapping to identify their structure.

We may see more research on these cannabinoids in the near future.

Some Novel Cannabinoids Include:

  • CBCV (cannabichromevarin)

  • CBDV (cannabidivarin)

  • CBE (cannabielsoin)

  • CBGM (cannabigerol monomethyl ether)

  • CBGV (cannabigerovarin)

  • CBL (cannabicyclol)

  • CBT (cannabicitran)

  • CBV (cannabivarin)

A Note On Synthetic Cannabinoids

There are also synthetic cannabinoids. These are compounds that are similar in shape and function to cannabinoids produced in our bodies, or in the cannabis plant.

It’s recommended that you stay far away from the synthetic cannabinoids — not only do they lack many of the medicinal actions of cannabis, they have the potential to cause serious harm.

The street drug known as “spice” is a combination of various synthetic cannabinoids. They were designed as an attempt to circumvent the legal hurdles preventing the sale of cannabis products for recreational use — and have since become a major cause of addiction and abuse.

+ Side-Effects of Synthetic Cannabinoid Use

  • Agitation and anxiety
  • Blurred vision
  • Chest pain
  • Death
  • Hallucinations
  • Heart attack
  • High blood pressure
  • Kidney failure
  • Nausea and vomiting
  • Paranoia
  • Psychosis
  • Racing heart
  • Seizures
  • Shortness of breath

+ List of Synthetic Cannabinoids

  • JWH-018
  • JWH-073
  • JWH-200
  • AM-2201
  • UR-144
  • XLR-11
  • AKB4
  • Cannabicyclohexanol
  • AB-CHMINACA
  • AB-PINACA
  • AB-FUBINACA
 
terpenes.jpg

Cannabis Terpenes

Terpenes are a class of compounds characterized by their volatile nature, and hydrocarbon-based structure. These are contained in high amounts in the essential oil of plants.

Terpenes have a very low molecular weight, and will evaporate under low temperatures. This, combined with their characteristic aromas is what gives many plants their scent. Conifer trees, fruits, and many flowers (including cannabis) all owe their aroma to their terpene profile.

Each plant can contains hundreds of different terpenes — many of which will even overlap into unrelated plant species. Cannabis shares terpenes with pine trees, many different flowers, citrus fruits, and nutmeg, among others.

Terpenes add flavor as well as additional medicinal benefits. Terpenes often have antibacterial, antiviral, antinflammatory, and anxiolytic effects.

+ List of Cannabis Terpenes

  • A-humulene
  • a-Terpenine
  • Alpha Bisabolol
  • alpha-Terpineol
  • Alpha/Beta Pinene
  • Beta-Caryophyllene
  • Bisabolol
  • Borneol
  • Camphene
  • Caryophyllene oxide
  • D-Linalool
  • Eucalyptol (1, 8 cineole)
  • Geraniol
  • Guaiol
  • Isopulegol
  • Limonene
  • Myrecene
  • Nerolidol
  • p-Cymene
  • Phytol
  • Pulegone
  • Terpineol-4-ol
  • Terpinolene
  • Trans Ocimene
  • Valencene
  • ∆-3-carene
 

Pharmacokinetics/Pharmacodynamics

Cannabinoids work by mimicking the endocannabinoids anandamide and 2-AG.

Endocannabinoids-anandamide-2-ag.jpg

Learn more about cannabinoid metabolism.

 

Clinical Applications of Cannabis

As an herb, cannabis is very useful. It works through a set of receptors most other plants don’t interact with — the endocannabinoid system.

The endocannabinoid system plays a major role in maintaining homeostasis. This gives cannabis an effect profile similar to adaptogens — but through different mechanisms.

Cannabis is similar to adaptogens in that it offers a bidirectional effect profile — which means it can both increase, and decrease tissue function according to its homeostatic baseline.

But cannabis isn’t quite an adaptogen because it can’t increase the bodies resistance to stress, and doesn’t appear to exert any action on the hypothalamus or adrenal glands directly.

Although cannabis has broad actions and therefore can provide benefit to a wide range of body systems — choosing the right product, strain, and phenotype for the job is critical.

An experienced herbalist or naturopath using cannabis will take into account the cannabinoid profile, terpene content, and anecdotal effects of each strain or CBD product being used.

Unlike other herbs, you have to be very particular about the type of cannabis being used for each condition.

What Constitutes “Medicinal” Cannabis?

There’s a big difference between using cannabis because “it’s healthy”, and using it as a therapeutic agent aimed at treating a specific disease process.

Although it can be used as both, daily supplementing cannabis or extracts like CBD don’t constitute medical cannabis.

However, you can use cannabis to address the symptoms, or underlying causes for some conditions.

 

Cautions:

Caution advised whenever using cannabis due to the potential for intoxicating side-effects. Without careful consideration of cannabinoid profile, some strains, or cannabis products may make symptoms for certain conditions worse — especially anxiety, psychosis, bipolar disorder, and insomnia.

 

Author

Justin Cooke, BHSc

The Sunlight Experiment

(Updated Jan 2019)

 

Recent Blog Posts:

References:

  1. Sharma P, Murthy P, Bharath M.M.S. (2012). Chemistry, Metabolism, and Toxicology of Cannabis: Clinical Implications. Iran J Psychiatry 2012; 7:4: 149-156

  2. Aizpurua-Olaizola, O., Soydaner, U., Öztürk, E., Schibano, D., Simsir, Y., Navarro, P., ... & Usobiaga, A. (2016). Evolution of the cannabinoid and terpene content during the growth of Cannabis sativa plants from different chemotypes. Journal of natural products, 79(2), 324-331.

  3. Shevyrin, V. A., & Morzherin, Y. Y. (2015). Cannabinoids: structures, effects, and classification. Russian Chemical Bulletin, 64(6), 1249-1266.

  4. De Petrocellis, L., Orlando, P., Moriello, A. S., Aviello, G., Stott, C., Izzo, A. A., & Di Marzo, V. (2012). Cannabinoid actions at TRPV channels: effects on TRPV3 and TRPV4 and their potential relevance to gastrointestinal inflammation. Acta physiologica, 204(2), 255-266.

  5. De Meijer, E. P. M., Hammond, K. M., & Micheler, M. (2009). The inheritance of chemical phenotype in Cannabis sativa L.(III): variation in cannabichromene proportion. Euphytica, 165(2), 293-311.

  6. Nelson, K., Walsh, D., Deeter, P., & Sheehan, F. (1994). A phase II study of delta-9-tetrahydrocannabinol for appetite stimulation in cancer-associated anorexia. Journal of palliative care.

  7. Bisogno, T., Hanuš, L., De Petrocellis, L., Tchilibon, S., Ponde, D. E., Brandi, I., ... & Di Marzo, V. (2001). Molecular targets for cannabidiol and its synthetic analogues: effect on vanilloid VR1 receptors and on the cellular uptake and enzymatic hydrolysis of anandamide. British journal of pharmacology, 134(4), 845-852.

  8. De Petrocellis, L., Vellani, V., Schiano-Moriello, A., Marini, P., Magherini, P. C., Orlando, P., & Di Marzo, V. (2008). Plant-derived cannabinoids modulate the activity of transient receptor potential channels of ankyrin type-1 and melastatin type-8. Journal of Pharmacology and Experimental Therapeutics, 325(3), 1007-1015.

  9. Cascio, M. G., Gauson, L. A., Stevenson, L. A., Ross, R. A., & Pertwee, R. G. (2010). Evidence that the plant cannabinoid cannabigerol is a highly potent α2‐adrenoceptor agonist and moderately potent 5HT1A receptor antagonist. British journal of pharmacology, 159(1), 129-141.

  10. Farrimond, J. A., Whalley, B. J., & Williams, C. M. (2012). Cannabinol and cannabidiol exert opposing effects on rat feeding patterns. Psychopharmacology, 223(1), 117-129.

  11. Pertwee, R. G. (2008). The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: Δ9‐tetrahydrocannabinol, cannabidiol and Δ9‐tetrahydrocannabivarin. British journal of pharmacology, 153(2), 199-215.

  12. Hollister, L. E. (1974). Structure-activity relationships in man of cannabis constituents, and homologs and metabolites of Δ9-tetrahydrocannabinol. Pharmacology, 11(1), 3-11.

  13. Pertwee, R. G. (2006). The pharmacology of cannabinoid receptors and their ligands: an overview. International journal of obesity, 30(S1), S13.

  14. Compton, D. R., Rice, K. C., De Costa, B. R., Razdan, R. K., Melvin, L. S., Johnson, M. R., & Martin, B. R. (1993). Cannabinoid structure-activity relationships: correlation of receptor binding and in vivo activitiesJournal of Pharmacology and Experimental Therapeutics265(1), 218-226.

  15. Burstein, S. (2005). PPAR-γ: a nuclear receptor with affinity for cannabinoids. Life sciences, 77(14), 1674-1684.García-Arencibia, M., González, S., de Lago, E., Ramos, J. A., Mechoulam, R., & Fernández-Ruiz, J. (2007). Evaluation of the neuroprotective effect of cannabinoids in a rat model of Parkinson's disease: importance of antioxidant and cannabinoid receptor-independent properties. Brain research, 1134, 162-170.

  16. Martín-Moreno, A. M., Reigada, D., Ramírez, B. G., Mechoulam, R., Innamorato, N., Cuadrado, A., & de Ceballos, M. L. (2011). Cannabidiol and other cannabinoids reduce microglial activation in vitro and in vivo: relevance to Alzheimers′ disease. Molecular pharmacology, mol-111.

  17. Dirikoc, S., Priola, S. A., Marella, M., Zsürger, N., & Chabry, J. (2007). Nonpsychoactive cannabidiol prevents prion accumulation and protects neurons against prion toxicity. Journal of Neuroscience, 27(36), 9537-9544.

  18. Malfait, A. M., Gallily, R., Sumariwalla, P. F., Malik, A. S., Andreakos, E., Mechoulam, R., & Feldmann, M. (2000). The nonpsychoactive cannabis constituent cannabidiol is an oral anti-arthritic therapeutic in murine collagen-induced arthritis. Proceedings of the National Academy of Sciences, 97(17), 9561-9566.

  19. Specter, S., Lancz, G., & Hazelden, J. (1990). Marijuana and immunity: tetrahydrocannabinol mediated inhibition of lymphocyte blastogenesis. International journal of immunopharmacology, 12(3), 261-267.

  20. Klein, T. W., Kawakami, Y., Newton, C., & Friedman, H. (1991). Marijuana components suppress induction and cytolytic function of murine cytotoxic T cells in vitro and in vivo. Journal of Toxicology and Environmental Health, Part A Current Issues, 32(4), 465-477.

  21. McCoy, K. L., Gainey, D., & Cabral, G. A. (1995). delta 9-Tetrahydrocannabinol modulates antigen processing by macrophages. Journal of Pharmacology and Experimental Therapeutics, 273(3), 1216-1223.

  22. Coffey, R. G., Yamamoto, Y., Snella, E., & Pross, S. (1996). Tetrahydrocannabinol inhibition of macrophage nitric oxide production. Biochemical pharmacology, 52(5), 743-751.

  23. Formukong, E. A., Evans, A. T., & Evans, F. J. (1988). Analgesic and antiinflammatory activity of constituents ofCannabis sativa L. Inflammation, 12(4), 361-371.

  24. Watzl, B., Scuderi, P., & Watson, R. R. (1991). Marijuana components stimulate human peripheral blood mononuclear cell secretion of interferon-gamma and suppress interleukin-1 alpha in vitro. International journal of immunopharmacology, 13(8), 1091-1097.

  25. Srivastava, M. D., Srivastava, B. I. S., & Brouhard, B. (1998). Δ9 tetrahydrocannabinol and cannabidiol alter cytokine production by human immune cells. Immunopharmacology, 40(3), 179-185.

  26. Pan, H., Mukhopadhyay, P., Rajesh, M., Patel, V., Mukhopadhyay, B., Gao, B., ... & Pacher, P. (2009). Cannabidiol attenuates cisplatin-induced nephrotoxicity by decreasing oxidative/nitrosative stress, inflammation, and cell death. Journal of Pharmacology and Experimental Therapeutics, 328(3), 708-714.

  27. Mecha, M., Feliú, A., Iñigo, P. M., Mestre, L., Carrillo-Salinas, F. J., & Guaza, C. (2013). Cannabidiol provides long-lasting protection against the deleterious effects of inflammation in a viral model of multiple sclerosis: a role for A2A receptors. Neurobiology of disease, 59, 141-150.

  28. Notcutt, W., Langford, R., Davies, P., Ratcliffe, S., & Potts, R. (2012). A placebo-controlled, parallel-group, randomized withdrawal study of subjects with symptoms of spasticity due to multiple sclerosis who are receiving long-term Sativex®(nabiximols). Multiple Sclerosis Journal, 18(2), 219-228.

  29. Woerly, S., Marchand, R., & Lavallée, G. (1991). Interactions of copolymeric poly (glyceryl methacrylate)-collagen hydrogels with neural tissue: effects of structure and polar groups. Biomaterials, 12(2), 197-203.

  30. Wade, D. T., Collin, C., Stott, C., & Duncombe, P. (2010). Meta-analysis of the efficacy and safety of Sativex (nabiximols), on spasticity in people with multiple sclerosis. Multiple Sclerosis Journal, 16(6), 707-714.

  31. Brady, C. M., DasGupta, R., Dalton, C., Wiseman, O. J., Berkley, K. J., & Fowler, C. J. (2004). An open-label pilot study of cannabis-based extracts for bladder dysfunction in advanced multiple sclerosis. Multiple Sclerosis Journal, 10(4), 425-433.

  32. Barnes, M. P. (2006). Sativex®: clinical efficacy and tolerability in the treatment of symptoms of multiple sclerosis and neuropathic pain. Expert opinion on pharmacotherapy, 7(5), 607-615.

  33. Leung, L. (2011). Cannabis and its derivatives: review of medical use. The Journal of the American Board of Family Medicine, 24(4), 452-462.

  34. Grotenhermen, F., & Müller-Vahl, K. (2012). The therapeutic potential of cannabis and cannabinoids. Deutsches Ärzteblatt International, 109(29-30), 495.

  35. Kwiatkoski, M., Guimaraes, F. S., & Del-Bel, E. (2012). Cannabidiol-treated rats exhibited higher motor score after cryogenic spinal cord injury. Neurotoxicity research, 21(3), 271-280.

  36. Chagas, M. H. N., Zuardi, A. W., Tumas, V., Pena-Pereira, M. A., Sobreira, E. T., Bergamaschi, M. M., ... & Crippa, J. A. S. (2014). Effects of cannabidiol in the treatment of patients with Parkinson’s disease: an exploratory double-blind trial. Journal of Psychopharmacology, 28(11), 1088-1098.

  37. Iuvone, T., Esposito, G., De Filippis, D., Scuderi, C., & Steardo, L. (2009). Cannabidiol: a promising drug for neurodegenerative disorders?. CNS neuroscience & therapeutics, 15(1), 65-75.

  38. Fernández‐Ruiz, J., Sagredo, O., Pazos, M. R., García, C., Pertwee, R., Mechoulam, R., & Martínez‐Orgado, J. (2013). Cannabidiol for neurodegenerative disorders: important new clinical applications for this phytocannabinoid?. British journal of clinical pharmacology, 75(2), 323-333.

  39. Yamaori, S., Kushihara, M., Yamamoto, I., & Watanabe, K. (2010). Characterization of major phytocannabinoids, cannabidiol and cannabinol, as isoform-selective and potent inhibitors of human CYP1 enzymes. Biochemical pharmacology, 79(11), 1691-1698.

  40. Yamaori, S., Maeda, C., Yamamoto, I., & Watanabe, K. (2011). Differential inhibition of human cytochrome P450 2A6 and 2B6 by major phytocannabinoids. Forensic Toxicology, 29(2), 117-124.

  41. Yamaori, S., Okamoto, Y., Yamamoto, I., & Watanabe, K. (2011). Cannabidiol, a major phytocannabinoid, as a potent atypical inhibitor for cytochrome P450 2D6. Drug Metabolism and Disposition, dmd-111.

  42. Yamaori, S., Ebisawa, J., Okushima, Y., Yamamoto, I., & Watanabe, K. (2011). Potent inhibition of human cytochrome P450 3A isoforms by cannabidiol: role of phenolic hydroxyl groups in the resorcinol moiety. Life sciences, 88(15-16), 730-736.

  43. Yamaori, S., Ebisawa, J., Okushima, Y., Yamamoto, I., & Watanabe, K. (2011). Potent inhibition of human cytochrome P450 3A isoforms by cannabidiol: role of phenolic hydroxyl groups in the resorcinol moiety. Life sciences, 88(15-16), 730-736.

  44. Koch, M., Dehghani, F., Habazettl, I., Schomerus, C., & Korf, H. W. (2006). Cannabinoids attenuate norepinephrine‐induced melatonin biosynthesis in the rat pineal gland by reducing arylalkylamine N‐acetyltransferase activity without involvement of cannabinoid receptors. Journal of neurochemistry, 98(1), 267-278.

  45. Jenny, M., Santer, E., Pirich, E., Schennach, H., & Fuchs, D. (2009). Δ9-Tetrahydrocannabinol and cannabidiol modulate mitogen-induced tryptophan degradation and neopterin formation in peripheral blood mononuclear cells in vitro. Journal of neuroimmunology, 207(1-2), 75-82.

  46. Takeda, S., Usami, N., Yamamoto, I., & Watanabe, K. (2009). Cannabidiol-2', 6'-dimethyl ether, a cannabidiol derivative, is a highly potent and selective 15-lipoxygenase inhibitor. Drug Metabolism and Disposition.

  47. Usami, N., Yamamoto, I., & Watanabe, K. (2008). Generation of reactive oxygen species during mouse hepatic microsomal metabolism of cannabidiol and cannabidiol hydroxy-quinone. Life sciences, 83(21-22), 717-724.

  48. Pertwee, R. G., Howlett, A. C., Abood, M. E., Alexander, S. P. H., Di Marzo, V., Elphick, M. R., ... & Mechoulam, R. (2010). International Union of Basic and Clinical Pharmacology. LXXIX. Cannabinoid receptors and their ligands: beyond CB1 and CB2. Pharmacological reviews, 62(4), 588-631.

Manuka (Leptospermum scoparium)

manuka-Leptospermum-scoparium-cover.jpg

What is Manuka?

In New Zealand, where manuka trees grow, the Maori consider male tea tree plants "Kanuka" and the female plants "Manuka". The plant is regarded very highly in this culture as a medicinal species.

The most well-known form of manuka is in manuka honey. This is a honey made by bees feasting primarily on manuka bushes. The honey has an impressive antibacterial profile when made from these plants. This is also reflected in the herb itself, which has been shown to have potent antibacterial, anti-fungal, and antiviral activity.

Most of the medicinal benefits of the plant come from its essential oil content, which can vary a lot depending on the region the plant was grown in.

 

What is Manuka Used For?

Internally, manuka is used to treat gastrointestinal conditions like diarrhea, colic, inflammatory bowel syndrome, and dysentery. It's also used for urinary tract infection, anxiety, and cold/flu infections.

Manuka is used topically for its antibacterial, and vulnerary actions. It's used to treat slow healing skin and bone injuries, bacterial infections, candida, and eczema. It can be gargled for gingivitis, or for general oral hygiene.

Manuka honey is another common form of the plant. It's become so popular worldwide, it's been standardised by the phenol content. This is expressed as a unique manuka factor (UMF) value set by the Active Manuka Honey Association (AMHA). Anything over UMF 5 is considered strong enough to kill MRSA.

 

Herb Details: Manuka

Herbal Actions:

  • Anti-inflammatory
  • Antibacterial
  • Antifungal
  • Antispasmodic
  • Anxiolytic
  • Diaphoretic
  • Diuretic
  • Febrifuge
  • Sedative
  • Astringent

Weekly Dose

Part Used

  • Leaves, Flowers, Bark

Family Name

  • Myrtaceae

Distribution

  • New Zealand

Constituents of Interest

  • Leptospermone
  • Sesquiterpenes
  • Tannins
  • Citronellal

Common Names

  • Manuka
  • Tea Tree
  • New Zealand Tea Tree

Quality

  • Neutral-Warm

Pregnancy

  • Unknown

Taste

  • Spicy

Duration of Use

  • Long term use is acceptable, but should be taken away from food.
 

Botanical Information

Manuka is a member of the Myrtaceae family of plants. This family contains as many as 133 different genera, and around 3800 different species, many of which are medicinally relevant.

 

Clinical Applications Of Manuka:

Manuka is useful both internally and topically. It's been shown to be an effective antibacterial agent for various forms of bacteria (including Staphylococcus). It's also an effective anti-fungal and antiviral (including HSV). The antibacterial effects were the most notable, with only some chemotypes of Manuka showing potent anti-fungal benefits.

Manuka can be used for nearly any form of bacterial infections both topically and internally, as well as wounds, ulcers, and gastrointestinal inflammation or infection. It's also useful for skin inflammation like eczema or psoriasis. The muscle relaxant effects make it useful for injuries, muscle tension, colic, and insomnia.

 

Cautions:

Manuka is widely considered safe and there are no common side effects of the herb.

+ Contraindications

Avoid long-term use alongside food. Tannins may impede mineral absorption.

 

Author:

Justin Cooke, BHSc

The Sunlight Experiment

(Updated November 2018)

 

Recent Blog Posts:

Mullein (Verbascum thapsus)

mullein-verbascum-thapsus-cover.jpg

Mullein

Mullein is considered a staple in herbal medicine. It wasn't native to North America and was brought over by European settlers. Despite the new introduction of the herb, it was quickly adopted into use by the local native Americans and is even referred to commonly as Indian Tobacco.

Mullein is a very safe herb and offers benefits to a number of different systems in the body.

Out of all systems, mullein is most commonly used for respiratory and digestive system conditions. It's popular as an anti-catarrhal and for both soothing dry coughs, and eliminating catarrh with productive coughs. Although the entire plant can be used for either one, the leaves are generally preferred for dry coughs and the roots for productive coughs.

Mullein is as useful topically as it is internally for inflammation, muscle spasms, and infection.

 

What Is Mullein Used For?

Mullein is mainly used for treating respiratory infections and persistent coughs. Somewhat ironically, it's often smoked for its soothing effect on the lungs. It tends to increase moisture in the lungs, especially the leaves, making it especially useful for unproductive, dry coughs.

It's also used for gastrointestinal inflammation, parasitic infection, and muscle aches. It tends to have a humidifying effect throughout the body, providing a soothing effect, especially with dryness.

One of the most well-known uses for the herb is in the form of an infused oil for ear infections.

 

Herb Details: Mullein

Main Herbal Actions:

  • Anthelmintic
  • Anti-catarrhal
  • Antispasmodic
  • Astringent
  • Expectorant
  • Lymphatic
  • Antibacterial

Weekly Dose

Part Used

  • Leaf, root, and flower

Family Name

  • Scrophulariaceae

Distribution

  • Originates from Europe around the Mediterranean, but has spread all around Europe & North America

Constituents of Interest

  • Iridoid glycosides

Common Names

  • Mullein
  • Lady's Flannel
  • Gordolobo
  • Punchón
  • Candelaria

Quality

  • Root: Neutral, drying
    Leaf: Cool, moistening
    Flower: Cool

Pregnancy

  • Unknown

Taste

  • Salty

Duration of Use

  • Long term use is acceptable.
 

Botanical Information

Mullein belongs to the figwort family (Scrophulariaceae) — a family consisting or roughly 65 different genera and 1800 species.

The Verbascum genus itself contains around 250 different species.

Verbascum is a popular garden plant for its ability to thrive in dry, nutrient-poor soils, and for their incredibly long flower duration.

The herb is biennial — the first season growing in a rosette leaf pattern, the second with a large velvety flower spike. Some mullein plants can grow up to three meters tall.

 

Clinical Applications Of Mullein:

Although there are many ways to use mullein, it excels with treating respiratory tract conditions. The leaves are excellent for treating dry coughs, while the root is much better for productive wet coughs.

Mullein is useful as a topical treatment for skin irritations, and as an oil for ear infections, especially the more drying flower of the plant.

Mullein also makes for an excellent lymphatic, both internally and externally.

 

Cautions:

Caution advised when working with the fresh leaf of this plant, as it can cause contact dermatitis in some individuals.

 

Author:

Justin Cooke, BHSc

The Sunlight Experiment

(Updated November 2018)

 

Recent Blog Posts:

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Frankincense (Boswellia) is one of the best anti-inflammatory herbs in our arsenal. It directly inhibits both COX and 5-LOX enzymes responsible for activating inflammatory messengers. This makes frankincense useful for conditions that involve inflammation as an underlying factor — such as indigestion, arthritis, pain, muscle injuries, or skin irritation.

Saw Palmetto (Serenoa repens)

Saw palmetto is a member of the palm tree family. The seeds of this plant are used to treat a variety of male aging problems like BPH, male pattern baldness, respiratory...

Turmeric (Curcuma longa)

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Walnut (Juglans nigra)

Walnut is a very versatile tree. The bark is used as a potent astringent, and the green, unripe husks make for a great antiparasitic agent. The husks can be extracted and made into...

Chinese Skullcap (Scutellaria baicalensis)

Skullcap is one of the best nervines on earth. The Chinese variety still has these nervine qualities, but is the best species for its anti-allergic, and antinflammatory...

Peppermint (Mentha piperita)

Peppermints volatile oil contains a rich source of the characteristic menthol. this chemical is often used as a flavouring agent. It is also a great carminative, and...

Licorice (Glycyrrhiza glabra)

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Marshmallow (Althaea officinalis)

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Sarsaparilla (Smilax spp.)

Sarsaparilla is a root found growing all over the world. It has a long history of use in both China and the South American Amazon rainforest for much the same uses...