scholarly journals Improvement of dermal parameters in aged skin after oral use of a nutrient supplement

2018 ◽  
Vol Volume 11 ◽  
pp. 195-201 ◽  
Author(s):  
Flavia Addor ◽  
Juliana Cotta Vieira ◽  
Camila Abreu
Keyword(s):  
Nutrient Supplement ◽  
Aged Skin

Effects of Mixed Dietary Supplements on Total Plasma Homocysteine Concentrations (tHcy): A Randomized, Double-Blind, Placebo-Controlled Trial

2012 ◽  
Vol 82 (4) ◽  
pp. 260-266 ◽  
Author(s):  
Salah E. Gariballa ◽  
Sarah J. Forster ◽  
Hilary J. Powers
Keyword(s):  
Older Patients ◽  
Controlled Trial ◽  
Plasma Homocysteine ◽  
Acute Illness ◽  
Vitamin B ◽  
Total Plasma ◽  
Double Blind ◽  
Double Blind Placebo ◽  
Nutrient Supplement ◽  
Plasma Thcy

Background: Although a number of studies have reported raised total plasma homocysteine (tHcy) concentrations in free-living older people, there are no data on homocysteine response to a mixed nutrient supplement in older patients. A raised plasma homocysteine concentration in older patients is partly a reflection of their co-morbidity, including impaired renal function, and there is uncertainty about the extent to which dietary interventions can improve plasma tHcy. Aim: To determine the plasma tHcy response to dietary supplements during acute illness. Methods: Two-hundred and thirty-six hospitalized, acutely ill older patients, who were part of a randomized double-blind placebo-controlled trial, were assigned to receive a daily oral nutritional supplement drink containing 1.3 mg of vitamin B2, 1.4 mg of vitamin B6, 1.5 μg of B12, 200 μg of folic acid, or a placebo, for 6 weeks. Outcome measures were plasma tHcy concentration at baseline, 6 weeks, and 6 months. Results: The mean plasma tHcy concentration fell among patients given the supplements (mean difference 4.1 µmol/L [95 % C.I, 0.14 to 8.03), p = 0.043], but tHcy concentration increased between 6 weeks and 6 months, after patients stopped taking the supplements [mean difference -2.0 µmol/L (95 % C.I, -03.9 to -0.18), p = 0.033]. About 46 % of patients in the placebo group and 55 % of patients in the supplement group had hyperhomocysteinemia (>14 µmol/L) at baseline compared with 45 % and 29 % at the end of the treatment period. Conclusions: A mixed nutrient supplement containing physiological amounts of B vitamins significantly reduced plasma tHcy concentrations in older patients recovering from acute illness.

scholarly journals Correction: Martinez-Fernandez et al. Seasonal and Nutrient Supplement Responses in Rumen Microbiota Structure and Metabolites of Tropical Rangeland Cattle. Microorganisms 2020, 8, 1550

2021 ◽  
Vol 9 (5) ◽  
pp. 1053
Author(s):  
Gonzalo Martinez-Fernandez ◽  
Jinzhen Jiao ◽  
Jagadish Padmanabha ◽  
Stuart E. Denman ◽  
Christopher S. McSweeney
Keyword(s):  
Rumen Microbiota ◽  
Nutrient Supplement ◽  
Microbiota Structure

We have found one inadvertent error in our paper published in Microorganisms [...]

HSP47, a collagen-specific chaperone protein, is a limiting factor for type I collagen secretion in aged skin

2017 ◽  
Vol 86 (2) ◽  
pp. e92
Author(s):  
MinJu Pyo ◽  
Jun Sang Park ◽  
Young Hun Lee ◽  
Dong Hun Lee ◽  
Jin Ho Chung ◽  
...  
Keyword(s):  
Type I Collagen ◽  
Limiting Factor ◽  
Type I ◽  
Chaperone Protein ◽  
Collagen Secretion ◽  
Aged Skin

Neuropeptides and skin aging

2013 ◽  
Vol 16 (1) ◽  
Author(s):  
Rana Elewa ◽  
Evgenia Makrantonaki ◽  
Christos C. Zouboulis
Keyword(s):  
Human Skin ◽  
Inflammatory Cytokines ◽  
Vasoactive Intestinal Polypeptide ◽  
Skin Aging ◽  
Target Cells ◽  
Hormone Metabolism ◽  
Skin Cells ◽  
Calcitonin Gene ◽  
Aged Skin ◽  
Human Skin Cells

AbstractNeuropeptides (NP) are peptides that are released as chemical messengers from nerve cells. They act either in an endocrine manner, where they reach their target cells via the bloodstream or a paracrine manner, as co-transmitters modulating the function of neurotransmitters. To date approximately 100 different NP have been described in the literature. In recent years, several studies have documented that human skin expresses several functional receptors for NP, such as corticotropin-releasing hormone, melanocortins, β-endorphin, vasoactive intestinal polypeptide, neuropeptide Y and calcitonin gene-related peptide. These receptors modulate the production of inflammatory cytokines, proliferation, differentiation, lipogenesis and hormone metabolism in human skin cells. In addition, several NP are directly produced by human skin cells, indicating the complexity of understanding the real functions of NPs in human skin. In this review we address the possible effects of neuropeptides on the pathogenesis of aged skin.

scholarly journals Fabrication of Tamarindus indica seeds extract loaded-cream for photo-aged skin: Visioscan® studies

2017 ◽  
Vol 4 ◽  
pp. 339-345 ◽  
Author(s):  
Muhammad Khurram Waqas ◽  
Barkat Ali Khan ◽  
Naveed Akhtar ◽  
Farzana Chowdhry ◽  
Haroon Khan ◽  
...  
Keyword(s):  
Tamarindus Indica ◽  
Aged Skin

scholarly journals Inflammatory Molecules Associated with Ultraviolet Radiation-Mediated Skin Aging

2021 ◽  
Vol 22 (8) ◽  
pp. 3974
Author(s):  
Tuba M. Ansary ◽  
Md. Razib Hossain ◽  
Koji Kamiya ◽  
Mayumi Komine ◽  
Mamitaro Ohtsuki
Keyword(s):  
Ultraviolet Radiation ◽  
Air Pollutants ◽  
Skin Aging ◽  
Environmental Stressors ◽  
Oxygen Species ◽  
Delayed Wound Healing ◽  
Different Types ◽  
Aged Skin ◽  
Inflammatory Molecules ◽  
Complex Organ

Skin is the largest and most complex organ in the human body comprised of multiple layers with different types of cells. Different kinds of environmental stressors, for example, ultraviolet radiation (UVR), temperature, air pollutants, smoking, and diet, accelerate skin aging by stimulating inflammatory molecules. Skin aging caused by UVR is characterized by loss of elasticity, fine lines, wrinkles, reduced epidermal and dermal components, increased epidermal permeability, delayed wound healing, and approximately 90% of skin aging. These external factors can cause aging through reactive oxygen species (ROS)-mediated inflammation, as well as aged skin is a source of circulatory inflammatory molecules which accelerate skin aging and cause aging-related diseases. This review article focuses on the inflammatory pathways associated with UVR-mediated skin aging.

Photodamaged and aged skin

2018 ◽  
pp. 179-184
Author(s):  
Anne-Sophie Brillouet ◽  
Michael D. Southall
Keyword(s):  
Aged Skin

scholarly journals UVA Exposure Combined with Glycation of the Dermis Are Two Catalysts for Skin Aging and Promotes a Favorable Environment to the Appearance of Elastosis

2021 ◽  
Vol 2021 ◽  
pp. 1-13
Author(s):  
Hervé Pageon ◽  
Hélène Zucchi ◽  
Sylvie Ricois ◽  
Philippe Bastien ◽  
Daniel Asselineau
Keyword(s):  
Protein Expression ◽  
Biological Effect ◽  
Skin Aging ◽  
Chronological Aging ◽  
Advanced Glycosylation End Products ◽  
Uva Irradiation ◽  
Inflammatory State ◽  
Aged Skin

Skin aging is the result of superimposed intrinsic (individual) and extrinsic (e.g., UV exposure or nutrition) aging. Previous works have reported a relationship between UV irradiation and glycation in the aging process, leading, for example, to modified radical species production and the appearance of AGEs (advanced glycosylation end products) in increasing quantities, particularly glycoxidation products like pentosidine. In addition, the colocalization of AGEs and elastosis has also been observed. We first investigated the combination of the glycation reaction and UVA effects on a reconstructed skin model to explain their cumulative biological effect. We found that UVA exposure combined with glycation had the ability to intensify the response for specific markers: for example, MMP1 or MMP3 mRNA, proteases involved in extracellular matrix degradation, or proinflammatory cytokine, IL1α, protein expression. Moreover, the association of glycation and UVA irradiation is believed to promote an environment that favors the onset of an elastotic-like phenomenon: mRNA coding for elastin, elastase, and tropoelastin expression is increased. Secondly, because the damaging effects of UV radiation in vivo might be more detrimental in aged skin than in young skin due to increased accumulation of pentosidine and the exacerbation of alterations related to chronological aging, we studied the biological effect of soluble pentosidine in fibroblasts grown in monolayers. We found that pentosidine induced upregulation of CXCL2, IL8, and MMP12 mRNA expression (inflammatory and elastotic markers, respectively). Tropoelastin protein expression (elastin precursor) was also increased. In conclusion, fibroblasts in monolayers cultured with soluble pentosidine and tridimensional in vitro skin constructs exposed to the combination of AGEs and UVA promote an inflammatory state and an alteration of the dermal compartment in relation to an elastosis-like environment.

scholarly journals Peptide location fingerprinting reveals modification-associated biomarkers of ageing in human tissue proteomes

2020 ◽  
Author(s):  
Matiss Ozols ◽  
Alexander Eckersley ◽  
Kieran T Mellody ◽  
Venkatesh Mallikarjun ◽  
Stacey Warwood ◽  
...  
Keyword(s):  
Structural Modification ◽  
Protein Structures ◽  
Cytoskeletal Proteins ◽  
Structural Modifications ◽  
Location Fingerprinting ◽  
Age Related ◽  
Analysis Technique ◽  
Key Factor ◽  
Aged Skin ◽  
Novel Biomarkers

AbstractAlthough dysfunctional protein homeostasis (proteostasis) is a key factor in many age-related diseases, the untargeted identification of structural modifications in proteins remains challenging. Peptide location fingerprinting is a proteomic analysis technique capable of identifying structural modification-associated differences in mass spectrometry (MS) datasets of complex biological samples. A new webtool (Manchester Peptide Location Fingerprinter), applied to photoaged and intrinsically aged skin proteomes, can relatively quantify peptides (spectral counting) and map statistically significant differences to regions within protein structures. New photoageing biomarkers were identified in multiple proteins including matrix components (collagens and proteoglycans), oxidation and protease modulators (peroxiredoxins and SERPINs) and cytoskeletal proteins (keratins). Crucially, for many extracellular biomarkers, structural modification-associated differences were not correlated with relative abundance (by ion intensity). By applying peptide location fingerprinting to published MS datasets, (identifying biomarkers including collagen V and versican in ageing tendon) we demonstrate the potential of the MPLF webtool to discover novel biomarkers.

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