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In addition to a significant decrease in hepatic lipid accumulation in the IOE group, which inhibited energy intake by propionate enrichment, hepatic lipids were also significantly reduced in the mice in the IOP group, which was largely enriched with butyrate. Compared with the IOE group, IOP had a stronger regulatory effect on hepatic metabolism and triglyceride metabolism and higher levels of TCA cycle in the host. In addition, butyrate has the ability to promote browning of white adipose tissue (WAT) to brown adipose tissue (BAT).^[@ref39],[@ref40]^ WAT stores energy, whereas BAT uses energy for heating and consequently host energy expenditure increases.^[@ref41],[@ref42]^ However, adipose tissue weight does not change after WAT browning.^[@ref43]^ Therefore, the weight of adipose tissue of mice in the IOP group dominated by butyrate was greater than that of the mice in the IOE group dominated by propionate.

In conclusion ([Figure [7](#fig7){ref-type="fig"}](#fig7){ref-type="fig"}C), the improvement of ob

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#!/usr/bin/env python
# -*- coding: utf-8 -*-

import datetime
import random

LEN = 5 
PREFIX = 'ct-dm-core-job-'

DIGITS = ''.join(str(x) for x in range(10))

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# Set Intel(R) Speed Shift Technology to Enabled
setup_var 0x4BC 0x1
# Set CFG Lock to Disabled
setup_var 0x4ED 0x0
# Set Above 4GB MMIO BIOS assignment to Enabled
# setup_var 0x79A 0x1

# Set EHCI Hand-off to Disabled
# setup_var 0x2 0x0
# Set XHCI Hand-off to Disabled

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#!/bin/bash

# You must accept the Oracle Binary Code License
# http://www.oracle.com/technetwork/java/javase/terms/license/index.html
# usage: get_jdk.sh <rpm|tar> <jdk_version>
# jdk_version: default 8
# rpm

EXT="rpm"
JDK_VERSION="8"