Previous Page  2 / 5 Next Page
Information
Show Menu
Previous Page 2 / 5 Next Page
Page Background

Volume 7, Issue 3 (Suppl)

J Gastrointest Dig Syst, an open access journal

ISSN: 2161-069X

Gastro 2017

June 12-13, 2017

Page 24

conference

series

.com

June 12-13, 2017 Rome, Italy

11

th

Global

GastroenterologistsMeeting

Francesco Marotta, J Gastrointest Dig Syst 2017, 7:3(Suppl)

DOI: 10.4172/2161-069X-C1-048

Hormetic microbiota effect on the gut-based mechanism of metformin benefit

M

etformin is commonly used as the first line of medication for the treatment of metabolic syndromes, such as obesity and

type 2 diabetes (T2D). Recently, this compound has gained an increasing interest within the scenario of pro-longevity

medicine given also its peculiar increase in AMP-activated protein kinase (AMPK) thus beneficially affecting energy balance

by maintaining a proper cellular AMP/ATP ratio through the increase of ATP consumption and decreasing ATP production,

which is associated with AMPK activation. The gut microbiota is known to play an important role in harvesting energy

from food, metabolic processes and immune modulation. An increasingly body of evidences proves that its composition is

significantly associated with obesity, T2D, metabolic syndromes and other chronic diseases. Data show that when metformin

is administered to high fat diet (HFD) animals, the composition of the phylum

Bacteroidetes

significantly increases (over

75%) similar to that in the normal diet-(ND)-fed animals. Moreover, the composition of

Verrucomicrobia

in the HFDMet

group significantly increases, unlike what obtained by simple dietary change applied to HFD. In the HFD-Met group, the

abundances of the families

Bacteroidaceae

,

Verrucomicrobia

ceae, and some specific

Clostridia

change significantly vs. those

in the HFD and HFD-ND groups. Interestingly, metformin treatment also affects the composition of the gut microbiota in mice

fed a ND. The families

Rikenellaceae, Ruminococcaceae

, and

Verrucomicrobia

ceae, as well as

Alistipes

spp.,

Akkermansia

spp., and Clostridium spp., are more abundant in the ND-Met group than the ND group. All this is shedding new light on

the AMPK-independent pathway of metabolic improvement by metformin treatment through targeting the microbiota. It is

likely that metformin via changes in

Akkermansia

and lactobacilli bacteria regulation improves the metabolic profile of diet-

induced obesity by ameliorating low-grade tissue inflammation and also up-regulating the intestinal expression of several

endocannabinoids controlling inflammation, barrier function and peptide secretion in the gut. Till recently, a main hindrance in

bacterial stool culture is represented by the major bias that only a few gut bacteria can be properly detected and cultivated in the

laboratory. On the other hand, capillary sequencing or PCR-based approaches need culture medium with its inner complexities

of multiple separate analyses. In this scenario, a rising star is represented by the next-generation sequencing (NGS) which by

combining multiple samples in a sequencing run, is able to analyse the entire microbial community within a sample. Thus,

this unique ability enables to catalog resident organisms within the very complex gut poly-microbial bacterial communities to

make a DNA-stable sampling and producing a report intelligible to physicians and ideally endowed with a nutritionist and a

gastroenterologist commented interplay so to make it a valid diagnostic, a treatment-guided result and a follow up tool as well.

This has been quite recently achieved by a spin off dedicated geneticists and biologists (Next Genomics, Prato, Italy) using a

kit allowing small and 14-day stable sampling of 0,0001% accuracy. This test is currently used also in clinical center (MMC

Milano, Milan, Italy) identifying the enterotype and the presence of bacterial species correlated with diseases.

Biography

Francesco Marotta completed his MD and PhD with experience in Gastroenterology, Oxidative Stress, Aging and Nutrigenomics in USA, Cape-Town and Japan leading to

extensive publications. He is a Research Professor in Department of Nutrition, Texas Women University, USA. He is in Advisory Board Panel of the Center for Life Science

at Nazarbayev University, Kazakhstan and he is an External Examiner at McGill University, Canada and Osaka University, Japan. Currently, he serves as CMO at Milano

Medical Center for Healthy Aging and also at a prime international clinical set up in central-Asia.

fmarchimede@libero.it

Francesco Marotta

1

ReGenera Research Group for Aging Intervention, Italy

2

NextGenomics Research Lab, Italy