Vitam Horm. 2011 ; 86: 217-237. doi:10.1016/B978-0-12-386960-9.00009-5.
Sif Hansdottir, MD, MS and Martha M. Monick, Ph.D.
Dept of Medicine, University of Iowa Carver College of Medicine and Veterans Administration Medical Center, Iowa City, IA 52242
I, Henry Lahore, have been using Vitamin D topically with great success for many years.
In general local application of Vitamin D appears to be at least 10 times better than if taken orally
Just a few weeks ago (Oct, 2016) I wondered if Vitamin D could be applied locally to the lungs
There are many low-cost ($10-30) nebulizers on Amazon which put a very fine mist with ultrasonics -115KHz) , 0.5 to 5 micrometer
New version in 2017 own 10 inhalers as of June 2019 them in 2018
It might be possible to just put some water-soluble vitamin D powder into water in an atomizer
A Vitamin D inhaler/atomizer/nebulizer might be very useful for some kinds of respiratory problems -such as
Asthma, Pneumonia, Wheezing, COPD, Respiratory Tract Infections, respiratory allergies, second-hand smoke, . .
3 million molecules of Vitamin D per alveoli (500 million alveoli in lungs, 1.5 trillion molecules in 40 IU of Vit D)
Update Nov 2016: Inhaled Vitamin D water from purchased nebulizer - lungs feel much better in < 1/2 hour.
Dec 4: continuing to use it daily. Guess: I inhale 500 IU of vitamin D in 30 seconds
Powder of 50,000 IU Vitamin D capsule dissolved in 5 tablespoons of water
Pour off or filter the water thru a coffee filter so as to keep the cellulose from clogging the inhaler
Update 2018 - switched to using Vitamin D Emulsion
2 parts water to 1 part Vitamin D emulsion ==> inhaler
1 of the sources of Vitamin D emulsion Amazon
Update 2019: >10 companies making nebulizers and >10 companies making Vitamin D emulsions
Surface area of lungs + nose = 8X more than the small intestines
|Nasal passages which include microvilli||160|
|Small Intestines - where oral Vitamin D is absorbed||30|
See also VitaminDWiki
- Who said vitamin D could not be patented
- Has details on 2012 International patent for inhaling Vitamin D POWDERS - no apparent conflict with Vitamin D emulsions/liquids
- Perhaps drugs such as inhaled vitamin D can get directly to the brain – March 2018
- Largest cause of infant deaths is respiratory infections, which is associated with low vitamin D – April 2011
- Antimicrobial implications of vitamin D – Oct 2011
- Respiratory infections cut in half by 20,000 IU weekly vitamin D if initially deficient – RCT March 2015
- Childhood asthma still reduced 4 months after 800 IU of Vitamin D daily - RCT Feb 2016
- COPD reduced by 40 percent with monthly 100,000 IU of vitamin D – RCT Jan 2015
Wonder how many days it would take to reduce Asthma or COPD if Vitamin D were inhaled?
- Inhaled vitamin D helped lungs of new-born (rats) – Dec 2016
This is the paper which got me thinking about inhaled vitamin D
- Lung cells activate Vitamin D, without liver or kidney – Nov 2016
- Vitamin D sprayed inside cheeks 2X more response (poor gut) – RCT Oct 2015
- Topical vitamin D might be more bio-available than oral – Oct 2015
See also VitaminDWiki - activation outside of the lungs, liver-kidneys
- Vaginal Vitamin D reduced vaginal infections - Jan 2014 another local application
- Malignant melanoma may be reduced by skin-activated vitamin D – Nov 2016
- The eyes can also activate vitamin D – Feb 2014
- PhD Dissertation - Local production of active vitamin D inhibits Prostate Cancer – Oct 2012
- Kidney not essential for Vitamin D3 activation – fungi can do it – Jan 2014
- Bones can activate vitamin D – July 2013
- Perhaps even mitochondria can activate vitamin D – April 2013
- Eczema (Atopic Dermatitis) treated by 1600 IU of vitamin D – meta-analysis Dec 2016
- Itchy skin (pruritus) due to kidney disease was treated with topical vitamin D – April 2015
- Topical Vitamin D uses – Review March 2014
- Dental implants 10 percent better with topical vitamin D (in dogs) – Sept 2015
Emulsions on VitaminDWiki
Breathing category starts with the following
- Search VitaminDWiki for "Respiratory Tract Infection" 482 items as of Sept 2017
- Search VitaminDWiki for Pneumonia 1,360 items as of July 2019
- Search VitaminDWiki for BRONCHITIS 272 items as of July 2019
- Search VitaminDWiki for ASTHMA in title 184 items - June 2018
- COPD Overview
- Search VitaminDWiki for Wheeze 1150 items as of Dec 2018
- Search VitaminDWiki for "air pollution" 554 items as of May 2018
- Cystic Fibrosis category listing has
34 items along with related searches
- Air Pollution reduces Vitamin D
Note: Air Pollution reduces UVB and keeps people indoors, both reduce Vitamin D
- Smoking reduces vitamin D
Supplementing with Vitamin D will improve the health of smokers and might decease craving
- Overviews at VitaminDWiki: Allergy Lung Cancer TB Asthma Influenza Colds and flu Pneumonia Respiratory infections
Vitamin D can be converted to an activated form in most cell tissues: no gut, liver, or kidney needed
Our understanding of vitamin D metabolism and biological effects has grown exponentially in recent years and it has become clear that vitamin D has extensive immunomodulatory effects.
The active vitamin D generating enzyme, 1a-hydroxylase, is expressed by the airway epithelium, alveolar macrophages, dendritic cells and lymphocytes indicating that active vitamin D can be produced locally within the lungs.
Vitamin D generated in tissues is responsible for many of the immunomodulatory actions of vitamin D.
The effects of vitamin D within the lungs include increased secretion of the antimicrobial peptide cathelicidin, decreased chemokine production, inhibition of dendritic cell activation and alteration of T cell activation. These cellular effects are important for host responses against infection and the development of allergic lung diseases like asthma. Epidemiological studies do suggest that vitamin D deficiency predisposes to viral respiratory tract infections and mycobacterial infections and that vitamin D may play a role in the development and treatment of asthma. Randomized, placebo controlled trials are lacking but ongoing.
Section from the PDF
Humans get vitamin D through synthesis in the skin following UVB exposure and to a lesser extent from limited dietary sources. Vitamin D from the skin or diet is metabolized primarily in the liver to 25-hydroxyvitamin D3 (25D) (Ponchon, Kennan et al. 1969). 25Dis the “storage form” of vitamin D and is used to determine the vitamin D status of individuals.
The last and rate limiting step in the synthesis of “active” 1,25-dihydroxyvitamin D3 (1,25D) is catalyzed by the mitochondrial enzyme 1a-hydroxylase and is conventionally known to take place in the kidneys. Renal 1a-hydroxylase activity is under stringent regulation by parathyroid hormone, calcium, calcitonin, phosphorus and 1,25D itself (ZEHNDER, BLAND et al. 1999). Vitamin D is inactivated by the ubiquitous enzyme, 24- hydroxylase, whose expression is inducible by 1,25D, thus creating a negative feedback loop (Holick 2007). The biological effects of vitamin D are achieved through the regulation of gene expression mediated by the vitamin D receptor (VDR) (Baker, McDonnell et al. 1988). Active vitamin D binds to VDR and upon ligand binding, the receptor dimerizes with the retinoic X receptor (RXR) (MacDonald, Dowd et al. 1993). The VDR/RXR complex binds to vitamin D responsive elements (VDREs) within the promoter regions of vitamin D regulated genes (Sutton and MacDonald 2003).
It is increasingly recognized that localized synthesis of 1,25D rather than systemic production is responsible for many of the immune effects of vitamin D. Extra-renal expression of 1a-hydroxylase has been found in various cells of the immune system including alveolar macrophages (Adams, Sharma et al. 1983; Reichel, Koeffler et al. 1987), dendritic cells (Fritsche, Mondal et al. 2003; Hewison, Freeman et al. 2003; Sigmundsdottir, Pan et al. 2007) and lymphocytes (Chen, Sims et al. 2007; Sigmundsdottir, Pan et al. 2007) as well as in airway epithelia (Hansdottir, Monick et al. 2008) (Table 1). Locally formed 1,25D acts in an autocrine or paracrine fashion to modulate cell proliferation, cell differentiation and immune function (Bell 1998; Hewison, Burke et al. 2007; White 2008).
- Respiratory Epithelial Cells Convert Inactive Vitamin D to its Active Form Nov 2009 Full text online
- Active form of vitamin D actually counteracts the effects of cigarette smoke in the lab - March 2015
1α, 25-hydroxy vitamin D3 counteracts the effects of cigarette smoke in airway epithelial cells
Cellular Immunology, doi:10.1016/j.cellimm.2015.03.004
Ruhui Zhanga, Haijin Zhaoa, Hangming Donga, Fei Zoub, Shaoxi Caia, ,
a Department of Respiratory, Chronic Airways Diseases Laboratory, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China
b School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou 510515, China
Cigarette smoke extracts (CSE) alter calpain-1 expression via ERK signaling pathway in bronchial epithelial cells. 1α,25-dihydroxyvitamin D3 (1,25D3) inhibits cigarette smoke-induced epithelial barrier disruption.
This study was aimed to explore whether the 1,25D3 counteracted the CSE effects in a human bronchial epithelial cell line (16HBE). In particular, transepithelial electrical resistance (TER) and permeability, expression and distribution of E-cadherin and β-catenin, calpain-1 expression, and ERK phosphorylation were assessed in the CSE-stimulated 16HBE cells. The CSE induced the ERK phosphorylation, improved the calpain-1 expression, increased the distribution anomalies and the cleaving of E-cadherin and β-catenin, and resulted in the TER reduction and the permeability increase. The 1,25D3 reduced these pathological changes. The 1,25D3 mediated effects were associated with a reduced ERK phosphorylation.
In conclusion, the present study provides compelling evidences that the 1,25D3 may be considered a possible valid therapeutic option in controlling the cigarette smoke-induced epithelial barrier disruption.
PDF is available free at Sci-Hub 10.1016/j.cellimm.2015.03.004
- C. V. Pardeshi and V. S. Belgamwar, “Direct nose to brain drug delivery via integrated nerve pathways bypassing the blood-brain barrier: An excellent platform for brain targeting,” Expert Opinion on Drug Delivery, vol. 10, no. 7, pp. 957–972, 2013.
- W.-Y. Ong, S.-M. Shalini, and L. Costantino, “Nose-to-brain drug delivery by nanoparticles in the treatment of neurological disorders,” Current Medicinal Chemistry, vol. 21, no. 37, pp. 4247–4256, 2014.
- L. Illum, “Nasal drug delivery—possibilities, problems and solutions,” Journal of Controlled Release, vol. 87, no. 1-3, pp. 187–198, 2003.
- P. Khadka, J. Ro, H. Kim et al., “Pharmaceutical particle technologies: an approach to improve drug solubility, dissolution and bioavailability,” Asian Journal of Pharmaceutical Sciences, vol. 9, no. 6, pp. 304–316, 2014.
- V. Puri, “A study on nano emulsion (Emulgel),” International Journal of Advanced Pharmaceutical Sciences, vol. 1, no. 3, pp. 27–55, 2018
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