Tuesday, 1 July 2014

Oxytocin: An Aged Muscle Repair Assistant Agent?

Thesis 2014: Oxytocin , is FDA approved. Previously thought of a hormone for lactation and social behaviors  is advancing on a front driven by the realization that OCT receptors are throughout the body. Current studies are
  1. osteopenia, obesity feedback via hypothalamus stimulation via OCT injection
  2. thymus and t cell immunity axis
  3. muscle repair via stem cell stimulation
  4. 1 rat experiment- appears over expression of liver enzyme of oxytocinase is responsible for OCT destruction.


Muscle repair via stem cell stimulation

 
Careful here - "When the team looked closely at what was happening in the regenerating muscle cells, they found that oxytocin turns on a well-known cellular cascade that triggers growth and proliferation: the MAPK/ERK signaling pathway.  "
 
 
The Starting point
 
 http://www.ncbi.nlm.nih.gov/pubmed/24915299   Oxytocin is an age-specific circulating hormone that is necessary for muscle maintenance and regeneration.

Author information

  • 11] Department of Bioengineering, Stem Cell Center, QB3 Institute, UC Berkeley, Berkeley, California

Abstract

 
The regenerative capacity of skeletal muscle declines with age. Previous studies suggest that this process can be reversed by exposure to young circulation; however, systemic age-specific factors responsible for this phenomenon are largely unknown. Here we report that oxytocin-a hormone best known for its role in lactation, parturition and social behaviours-is required for proper muscle tissue regeneration and homeostasis, and that plasma levels of oxytocin decline with age. Inhibition of oxytocin signalling in young animals reduces muscle regeneration, whereas systemic administration of oxytocin rapidly improves muscle regeneration by enhancing aged muscle stem cell activation/proliferation through activation of the MAPK/ERK signalling pathway. We further show that the genetic lack of oxytocin does not cause a developmental defect in muscle but instead leads to premature sarcopenia. Considering that oxytocin is an FDA-approved drug, this work reveals a potential novel and safe way to combat or prevent skeletal muscle ageing.

Rate : 1microgram of OCT per gram of mouse ie 1miligram per kg of mouse ie 80mg per 80 kg mouse. Roughly equals  2mg per 80kg human using surface area multiplier.

Low Oxytocin,  Liver and Oxytocinase Activity


from this paper J Endocrinol. 2014 Feb 10;220(3):333-43.

Hypooxytocinaemia in obese Zucker rats relates to oxytocin degradation in liver and adipose tissue.

 http://www.ncbi.nlm.nih.gov/pubmed/24389591

 "Obese Zucker rats displayed a marked reduction in plasma oxytocin levels. Elevated liver and adipose tissue oxytocinase activity was noticed in obese Zucker rats. Hypothalamic oxytocin gene expression was not altered by the obese phenotype. OXTR mRNA and protein levels were upregulated in the adipose tissue of obese animals in contrast to the reduced OXTR protein levels in skeletal muscle. Our results show that obesity is associated with reduced plasma oxytocin due to increased peptide degradation by liver and adipose tissue rather than changes in hormone synthesis. This study highlights the importance of the oxytocin system in the pathogenesis of obesity and suggests oxytocinase inhibition as a candidate approach in the therapy of obesity."


Osteopenia and Obesity
Endocrinology. 2014 Apr;155(4):1340-52.

Oxytocin reverses ovariectomy-induced osteopenia and body fat gain.

http://www.ncbi.nlm.nih.gov/pubmed/24506069
Thus, OT constitutes an effective strategy for targeting osteopenia, overweight, and fat mass redistribution without any detrimental effects in a mouse model mimicking the menopause


Treatment of Obesity and Diabetes Using Oxytocin or Analogs in Patients and Mouse Models


http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658979/

 Here, based on a randomized pilot clinical trial, we report that intranasal oxytocin administration over an 8-week period led to effective reduction of obesity and reversal of related prediabetic changes in patients.
Figure 2
Human data




 http://iv.iiarjournals.org/content/24/2/157.full.pdf

 

Abstract.
Background: It has been shown that the
neurohypophyseal peptide oxytocin is present in the human
thymus and in vitro it can mimic interleukin (IL)-2 action in
the induction of interferon-γ production.he present results support the hypothesis that neuropeptides
may act as a link in the network between the immune and the
neuroendocrine systems
 http://www.ncbi.nlm.nih.gov/pubmed/19479077

 PLoS One. 2009 May 22;4(5):e5668. doi: 10.1371/journal.pone.0005668.

Impact of growth hormone (GH) deficiency and GH replacement upon thymus function in adult patients.

Abstract

BACKGROUND:

Despite age-related adipose involution, T cell generation in the thymus (thymopoiesis) is maintained beyond puberty in adults. In rodents, growth hormone (GH), insulin-like growth factor-1 (IGF-1), and GH secretagogues reverse age-related changes in thymus cytoarchitecture and increase thymopoiesis. GH administration also enhances thymic mass and function in HIV-infected patients. Until now, thymic function has not been investigated in adult GH deficiency (AGHD). The objective of this clinical study was to evaluate thymic function in AGHD, as well as the repercussion upon thymopoiesis of GH treatment for restoration of GH/IGF-1 physiological levels.

METHODOLOGY/PRINCIPAL FINDINGS:

Twenty-two patients with documented AGHD were enrolled in this study. The following parameters were measured: plasma IGF-1 concentrations, signal-joint T-cell receptor excision circle (sjTREC) frequency, and sj/beta TREC ratio. Analyses were performed at three time points: firstly on GH treatment at maintenance dose, secondly one month after GH withdrawal, and thirdly one month after GH resumption. After 1-month interruption of GH treatment, both plasma IGF-1 concentrations and sjTREC frequency were decreased (p<0.001). Decreases in IGF-1 and sjTREC levels were correlated (r = 0.61, p<0.01). There was also a decrease in intrathymic T cell proliferation as indicated by the reduced sj/beta TREC ratio (p<0.01). One month after reintroduction of GH treatment, IGF-1 concentration and sjTREC frequency regained a level equivalent to the one before GH withdrawal. The sj/beta TREC ratio also increased with GH resumption, but did not return to the level measured before GH withdrawal.

CONCLUSIONS:

In patients with AGHD under GH treatment, GH withdrawal decreases thymic T cell output, as well as intrathymic T cell proliferation. These parameters of thymus function are completely or partially restored one month after GH resumption. These data indicate that the functional integrity of the somatotrope GH/IGF-1 axis is important for the maintenance of a normal thymus function in human adults.

TRIAL REGISTRATION:

ClinicalTrials.gov NTC00601419.


HRV Early Explorations for AntiAging Clinicians

Wednesday, 25 June 2014

Plant Offal

Monday June 30th 2014
 
Dear M
 
It was a joy to see your face light up when I mentioned " Plant Offal" yesterday in Healesville!
 
naturally I cant find the actual story that used the term " plant offal"- its a good name
here are some links to that storyline....
 
 
and here is a link to a wonderful dementia  story airing on Australian Story now- both on Rupert Murdoch's tabloid paper out of the UK! 
 
Maybe Rupert should ask to become your new best friend.
 
all the best!
j

Thursday, 12 June 2014

June 2014 resources

  1. endogenous testosterone and SHBG with glycated haemoglobin in middle-aged and older men
  2. Stomach exercises 
  3. Scooter 
  4. staking plan 
  5. monash bloating gut professor 
  6. gut mucus and bacteria 
  7. pancreas mitochonrdria fatty acids  
  8. IBS story book 
  9. hook worms and vit c in gut 
  10. csiro starplus starch 
  11. hospital trial of starplus 
  12.  Jane Plant breaST CANCER PLANT DIET
  13. fast stimulates stem cell immunity 
  14. carbohydrate activates mouth nerves 
  15. Noakes carb resistant 
  16. fibre wiki 
  17.  In Arabidopsis, a high concentration of salicylic acid activates a molecular signal transduction pathway that is identified by a gene called nim1 (also known as npr1 or sai1). The pathway results in heightened immunity to all pathogens in uninfected parts of the plant, sometimes for many days after the attack....
  18.  In many plant species, resistance to pathogen infec- tion increases as a function of age; this phenomenon is often termed age-related resistance...
  19. Thus to inhibit COX-2, high doses of aspirin are required because of the decreased sensitivity of COX-2 to aspirin... 
  20.  Grape Exosomes
  21. 100 squats a day 
  22. CSIRO saturated fats paper good 
  23. Oxytocin in old mice repair of muscle damage 
  24. GOS prebiotic supports old human microbiota 
  25. Adrenaline increases white blood cell increase and artery hardening
  26.  Hippocratic writings
  27. Trehalose aging blog watson 
  28. Trehalose forum useful 
  29. Trehalose supplier swanson should go to garhill 
  30. trehalose japanese pape well just eat mushrooms
  31. Promethease
  32. Nimble scooter
  33. hullo pulse test hrv
  34. Pulse test
  35. pulse test checklist
  36. mcguff paper on hrv
  37. vital connect
  38. sweetwater hrv 101
  39. dry bread for Chrohns
  40. what would cassanova do?
  41. heart rate variability and sports
  42. termite specialist
  43.  

Monday, 26 May 2014

Nitrite skin bacteria gemma

 http://www.nytimes.com/2014/05/25/magazine/my-no-soap-no-shampoo-bacteria-rich-hygiene-experiment.html?smid=pl-share
my-no-soap-no-shampoo-bacteria-rich-hygiene-experiment. 


Gemma says:
There was perhaps too much nitrogen in my original comment, so here goes some science to de-confuse the dear reader (on the interplay of sun, nitrogen, ammonia-oxidizing bacteria and CVD health):
Is sunlight good for our heart?
“We propose here that many of the beneficial effects of sunlight, particularly those related to cardiovascular health, are mediated by mechanisms that are independent of melatonin, vitamin D, and exposure to UVB alone. Specifically, we suggest that the skin is a significant store of nitric oxide (NO)-related species that can be mobilized by sunlight and delivered to the systemic circulation to exert coronary vasodilator and cardioprotective as well as antihypertensive effects (Figure 1). We further hypothesize that this dermal NO reservoir is a product of local production and dietary supply with nitrate-rich foods.
[...]
A recent human study has demonstrated that UVA irradiation can increase plasma nitrite levels by 40%. This is intriguing considering that in animal models, a similar increase in nitrite is associated with cardioprotection following I/R injury. Dietary nitrate intake (predominantly from green leafy vegetables) may provide an alternative source of nitrite.”
http://eurheartj.oxfordjournals.org/content/early/2010/03/09/eurheartj.ehq069.full

 Gemma says:
And now on the importance of the ammonia oxidising bacteria (AOB) living on the skin:
Soil bacteria, nitrite and the skin
“Mammals likely evolved with AOB on their skin, providing their host with nitrite by conversion of ammonia in providing their host with nitrite by conversion of ammonia in sweat with scalp, pubic and underarm hair providing a suitable niche due to enhanced sweat production, increased warmth, increased relative humidity and protection of light (the latter is important as ammonia monooxygenase activity is inhibited by light). Low NO increases androgen levels which increase growth of pubic hair, expanding the AOB niche thereby increasing NO/NOx production and absorption in a feedback loop.
The production of a suitable niche for these bacteria provides a rationale for non-thermal sweating (e.g., under stress) (to supply NO/nitrites, the location of body hair (near lymph nodes), why the skin of the scalp is thin and well vascularized (to enhance NO/nitrite absorption), any why the sweat glands are most abundant on the feet and palms (fro antimicrobial effects of acidified nitrite in surfaces in contact with soil).
http://www.researchgate.net/publication/227124248_Soil_bacteria_nitrite_and_the_skin
(full text available)

Sunday, 18 May 2014

Grace Conversations

l
l
  1. GI stool 2200
  2. Mitoq10 intro
  3. Cambridge digestion of starch
  4. Dalton Hamstring Strech
  5. Organic straved beetroot have better anti cancer effect
  6. Amla for dog pancreatitis
  7. Salicin for skin and gut
  8. DHL for 23and me
  9. Arab plant circadian cycle salicin midnight
  10. Polly matzinger forum cnacer
  11. bolon cancer relapse
  12. Banana mitogen
  13. Grace slide show UK colon cancer
  14. CAPP aspirin
  15. Boots No 7’s new Protect & Perfect Advanced Serum,
  16. Shao Ping sour dough
  17. Browning white fat cells
  18. Pot Citrate Beetroot powder melbourne
  19. Beetroot Bread
  20. Fusobacterium colon cancer dental
  21. Ultrasound cheap for blood flow to brain ebay 160$
  22. GDF11
  23. thesis gene-scfa-fat
  24. broccli helps colitis DSS attack
  25. Thiamin lonsdale 


1 to 20 of 22

Selected: 11
1.
Paterson JR, Srivastava R, Baxter GJ, Graham AB, Lawrence JR.
J Agric Food Chem. 2006 Apr 19;54(8):2891-6.
PMID:
16608205
[PubMed - indexed for MEDLINE]
2.
Baxter GJ, Graham AB, Lawrence JR, Wiles D, Paterson JR.
Eur J Nutr. 2001 Dec;40(6):289-92.
PMID:
11876493
[PubMed - indexed for MEDLINE]
3.
Baxter GJ, Lawrence JR, Graham AB, Wiles D, Paterson JR.
Ann Clin Biochem. 2002 Jan;39(Pt 1):50-5.
PMID:
11853189
[PubMed - indexed for MEDLINE]
4.
Lawrence JR, Peter R, Baxter GJ, Robson J, Graham AB, Paterson JR.
J Clin Pathol. 2003 Sep;56(9):651-3.
PMID:
12944546
[PubMed - indexed for MEDLINE]
Free PMC Article
5.
Duthie GG, Kyle JA, Jenkinson AM, Duthie SJ, Baxter GJ, Paterson JR.
J Agric Food Chem. 2005 Apr 20;53(8):2897-900.
PMID:
15826036
[PubMed - indexed for MEDLINE]
6.
Paterson J, Baxter G, Lawrence J, Duthie G.
Proc Nutr Soc. 2006 Feb;65(1):93-6. Review.
PMID:
16441948
[PubMed - indexed for MEDLINE]
7.
McCreadie RG, Kelly C, Connolly M, Williams S, Baxter G, Lean M, Paterson JR.
Br J Psychiatry. 2005 Oct;187:346-51.
PMID:
16199794
[PubMed - indexed for MEDLINE]
Free Article
8.
Paterson SG, Robson JE, McMahon MJ, Baxter G, Murphy MJ, Paterson JR.
Ann Clin Biochem. 2006 Sep;43(Pt 5):369-71.
PMID:
17022878
[PubMed - indexed for MEDLINE]
9.
Wood A, Baxter G, Thies F, Kyle J, Duthie G.
Mol Nutr Food Res. 2011 May;55 Suppl 1:S7-S14. doi: 10.1002/mnfr.201000408. Epub 2011 Feb 23. Review.
PMID:
21351247
[PubMed - indexed for MEDLINE]
10.
Mitra A, Hannay D, Kapur A, Baxter G.
Prim Health Care Res Dev. 2011 Oct;12(4):329-34. doi: 10.1017/S1463423611000193.
PMID:
22284947
[PubMed - indexed for MEDLINE]
11.
Shaukat A, Grau MV, Church TR, Baxter G, Barry EL, Summers R, Sandler RS, Baron JA.
Cancer Epidemiol Biomarkers Prev. 2011 Apr;20(4):679-82. doi: 10.1158/1055-9965.EPI-10-1135. Epub 2011 Feb 9.
PMID:
21307305
[PubMed - indexed for MEDLINE]
Free PMC Article