ライフサイエンスコーパス: epididymal

1 g-1 was induced in subcutaneous (9-fold) and epididymal (4-fold) fat pads from db/db mice treated for

2 , less hepatosteatatitis, and a reduction in epididymal adipocyte volume.

3 afficking kinetics of GLUT4 and GLUT1 in rat epididymal adipocytes were analyzed by a four-compartmen

4 In rat epididymal adipocytes, practically all of the major gluc

5 o suppress lipolysis from mesenteric but not epididymal adipocytes.

6 ody weight gain, more severe inflammation in epididymal adipose tissue (EAT), and aggravated insulin

7 fat diet (HFD) has major effects on visceral epididymal adipose tissue (eWAT).

8 GLUT4 and adiponectin protein expression in epididymal adipose tissue and increased blood glucose co

9 ced transcription of the adiponectin gene in epididymal adipose tissue but not in subcutaneous fat.

10 IL-6 and IL-10, and CXCL chemokines in white epididymal adipose tissue from both wt and AhRR Tg mice.

11 Epididymal adipose tissue from wild-type mice produced a

12 body fat content as well as the quantity of epididymal adipose tissue of male Wistar rats was decrea

13 ide palmitate in HC- versus CF-fed mice, the epididymal adipose tissue synthesized approximately 1.5-

14 in to stimulate leptin release from isolated epididymal adipose tissue was also enhanced in R6/2 mice

15 ed rates of in vivo triglyceride turnover in epididymal adipose tissue were measured using (2)H(2)O a

16 es of metabolite carbon atoms taken from rat epididymal adipose tissue, goosefish islet cells, Coryne

17 intracellular peptides in gastrocnemius and epididymal adipose tissue, which likely is involved with

18 ectin immunoprecipitated from adipocytes and epididymal adipose tissue.

19 f insulin to stimulate glucose metabolism in epididymal adipose tissue.

20 leptin mRNA at a level comparable to that in epididymal adipose tissue.

21 own-like adipocytes in subcutaneous, but not epididymal, adipose depots.

22 ssed adiposity levels, leptin mRNA levels in epididymal and inguinal white adipose tissue (EWAT and I

23 In epididymal and mesenteric adipose tissue of control rats

24 ue-Dawley rats to either surgical removal of epididymal and perinephric fat pads (VF-; n = 9) or a sh

25 Epididymal and perirenal adipocyte size was increased 20

26 reduction of approximately 60% in weight of epididymal and perirenal depots.

27 plasma leptin levels and a >50% reduction in epididymal and perirenal fat pad size.

28 into BAT resulted in profound reductions in epididymal and retroperitoneal WAT mass, without affecti

29 clamp as well as in adipocytes isolated from epididymal and subcutaneous adipose tissue.

30 ession also is significantly elevated in the epididymal and subcutaneous fat pads from ob/ob mice com

31 fat diet (HFD) upregulated pfn expression in epididymal and subcutaneous white adipose tissue (WAT) b

32 on, by recording CatSper currents from human epididymal and testicular spermatozoa, we show that CatS

33 Inguinal, epididymal, and retroperitoneal fat pads weighed less in

34 significantly smaller in HFpEF than in sham (epididymal AT, 7.59 versus 10.67 mg/g; inguinal AT, 6.34

35 matory cytokines TNF-alpha or osteopontin in epididymal ATMs of obese mice caused significant improve

36 in obese mice selectively silences genes in epididymal ATMs, whereas macrophages within lung, spleen

37 ructural defects were found in two-thirds of epididymal axonemes, with the most common abnormality be

38 a13, and Id2) in murine brown, inguinal, and epididymal (BAT, iWAT, and eWAT) adipose tissues.

39 Expansion of white adipose tissue-derived epididymal BK(L1/L1) preadipocytes and their differentia

40 Therewith, Trpv6 excision affects epididymal Ca(2+) handling and male fertility to the sam

41 Sperm extracted from the epididymal cauda showed strongly impaired motility chara

42 e employed expression screening of a hamster epididymal cDNA library to obtain the full-length sequen

43 Epididymal clear cells contain abundant V-ATPase in thei

44 In both kidney-intercalated cells and epididymal clear cells, cAMP induces V-ATPase apical mem

45 responding murine genes, indicating that the epididymal cluster is evolutionary conserved.

46 collectively with testosterone to facilitate epididymal coiling by stimulating epithelial proliferati

47 This loss of epididymal coiling did not result from testosterone defi

48 chromocytomas, endolymphatic sac tumors, and epididymal cystadenomas.

49 We previously have shown that the epididymal cystatin CRES (cystatin-related epididymal sp

50 ns indicate that cSrc is essential for cauda epididymal development and suggest an essential role of

51 verexpression triggers male sterility due to epididymal dysfunction caused by epithelial disorganizat

52 lity, we assessed metabolism and measures of epididymal (e)WAT mitochondria and artery function in yo

53 intraperitoneal insulin tolerance tests, and epididymal (eAT) and inguinal subcutaneous AT (iAT) and

54 tiate an immune response if they escaped the epididymal environment.

55 murine subcutaneous (SC) or intra-abdominal epididymal (EP) white adipocytes.

56 odeling of the glycocalyx of spermatozoa and epididymal epithelial cells by endogenous sialidases aft

57 llent model to study the role of Sertoli and epididymal epithelial cells in the differentiation and m

58 on of miR-29a inhibited the proliferation of epididymal epithelial cells in vitro.

59 om defects in the functioning of Sertoli and epididymal epithelial cells.

60 rize the sialylation of the apical region of epididymal epithelial cells.

61 s also observed in primary cultures of mouse epididymal epithelial cells.

62 functions of the TRPV6(D541A) pore mutant in epididymal epithelial cells.

63 ms, CAII and CAIV, are distributed along the epididymal epithelium and appear with the onset of puber

64 ese males show extensive degeneration of the epididymal epithelium in the corpus region, rather than

65 We have shown that Bmp7 expression in epididymal epithelium is developmentally regulated.

66 cSrc is enriched in vesicles released by the epididymal epithelium known as epididymosomes.

67 requirement of different classes of BMPs for epididymal epithelium to survive and have significant im

68 Bmp8atm1 males also show degeneration of the epididymal epithelium, indicating a novel role for BMPs

69 ls in mice disrupts Ca(2+) absorption by the epididymal epithelium, resulting in abnormally high Ca(2

70 ay originate from sperm, instead of from the epididymal epithelium.

71 s mirrored by a lack of Ca(2+) uptake by the epididymal epithelium.

72 In terms of the cluster ancestry, epididymal expression possibly appeared in a PGDS-like l

73 veral strong bands on Western blots of human epididymal extracts from the caput and corpus regions.

74 plete their maturation; however, no specific epididymal factors that mediate this process have so far

75 ositol-3'-kinase (PI-3-kinase) expression in epididymal fat (26% decrease; P < 0.1).

76 <0.01) less retroperitoneal, mesenteric, and epididymal fat accumulation, compared to their ob/ob cou

77 ethylation of its promoter in progenitors of epididymal fat compared to Con offspring, which was corr

78 el was lower in human visceral fat and mouse epididymal fat compared with their subcutaneous fat.

79 at 6 mo) and had significantly more (P<0.01) epididymal fat content.

80 leasable and extractable LPL activity in the epididymal fat decreased by 75-80% in the diabetic group

81 lation of Foxa3 have a selective decrease in epididymal fat depot and a cell-autonomous defect to ind

82 rger cells (120-160 microm; P < 0.05) in the epididymal fat depot.

83 tissue (VAT) of lean mice, especially in the epididymal fat depot.

84 that regulates the selective enlargement of epididymal fat depots and suppresses energy expenditure

85 depot could affect vascular disease in mice, epididymal fat depots were transplanted into atheroscler

86 se in the diet, whereas [(3)H]NE turnover in epididymal fat did not respond to either monosaccharide.

87 in GLUT4 (54 +/- 5% of high-carbohydrate) in epididymal fat from rats on the high-fat diet for 3 week

88 During HFD feeding, epididymal fat initiates adipogenesis after 4 weeks, whe

89 Thus, the rapid increase in epididymal fat mass with the cessation of voluntary whee

90 Absolute and relative epididymal fat mass, mean cell volume, and amount of lip

91 NA methylation in the zfp423 promoter in the epididymal fat of OB/Obe offspring, which was correlated

92 in confined well-vascularized sites like the epididymal fat pad (EFP) improved graft outcomes, but on

93 Micro) in the confined and well-vascularized epididymal fat pad (EFP) site, a model of the human omen

94 ouse islets engrafted on the intra-abdominal epididymal fat pad ameliorated streptozotocin-induced hy

95 ia occurred in all mice after removal of the epididymal fat pad bearing the islet graft.

96 This study indicates that the epididymal fat pad maybe a useful islet transplant site

97 eeded scaffolds were then implanted onto the epididymal fat pad of syngeneic mice with streptozotocin

98 The epididymal fat pad was evaluated as a site of islet tran

99 t affected until week 28 (decreased by 14%); epididymal fat pad weight also decreased (25%) at this t

100 yperleptinemia and reduction in food intake, epididymal fat pad weight declined 55% in wild-type but

101 air-fed group, a significant increase in the epididymal fat pad weight, BAT weight, and plasma leptin

102 A significant increase in the epididymal fat pad weight, interscapular brown adipose t

103 ell as lower hepatic triglyceride levels and epididymal fat pad weights than in SHR harboring mutant

104 3) Does short-term elimination of T cells in epididymal fat pad without disturbing the systemic T cel

105 o the devices, which were implanted into the epididymal fat pad(s) of streptozocin diabetic mice.

106 er visceral adipose tissue mass estimated by epididymal fat pad, associated with iron accumulation in

107 w as 50 islets, either intraportal or in the epididymal fat pad, displayed similar glucose tolerance

108 ic mass of syngeneic islets implanted in the epididymal fat pad, followed by a subrenal capsular impl

109 that for M-CPT I in RNA isolated from whole epididymal fat pad, this was reversed in purified adipoc

110 mia and increased homocysteine levels in the epididymal fat pad, which was associated with decreased

111 cally, adiponectin KO mice possessed smaller epididymal fat pads and showed reduced body weight compa

112 To determine the mechanism, epididymal fat pads from normal wild-type (+/+) and obes

113 Acute depletion of T cells from epididymal fat pads improved insulin action in young DIO

114 have greater deposits of s.c. fat and larger epididymal fat pads in comparison with wild-type mice.

115 PPARgamma-regulated genes were higher in the epididymal fat pads of Adipoq-LPL mice than control mice

116 .4-microm pore membranes when implanted into epididymal fat pads of rats.

117 adipocytes from SPARC-null versus wild-type epididymal fat pads were 252 +/- 61 and 161 +/- 33 micro

118 stablish feasibility of fat transplantation, epididymal fat pads were harvested from wild-type C57BL/

119 Incubation of epididymal fat pads with leptin or its i.v. injection in

120 ties, including low fertility, an absence of epididymal fat pads, and a tendency to develop blepharit

121 nd in primary adipocytes isolated from mouse epididymal fat pads, in response to acute activation of

122 ere found to have lower body weight, smaller epididymal fat pads, lower blood levels of nonesterified

123 n messenger RNA (mRNA) and protein levels in epididymal fat pads.

124 that GSK-3 activity increased twofold in the epididymal fat tissue and remained unchanged in muscle a

125 ntrast, GSK-3 activity did not change in the epididymal fat tissue of A/J mice, regardless of the typ

126 th reduced levels of the pP65 protein in the epididymal fat tissue, suggesting less activation of the

127 1 protein levels were significantly lower in epididymal fat tissues from db/db and high fat diet-indu

128 is associated with a prolonged overshoot in epididymal fat triacylglycerol synthesis.

129 The rate of triacylglycerol synthesis in epididymal fat was 4.2-fold greater in SED5 than in WL5,

130 C/EBPalpha protein levels in epididymal fat were 30% greater in SED5 than in WL5.

131 H2O content and wt of epididymal fat were increased by RSG and correlated to i

132 t and GSK3 phosphorylation and activities in epididymal fat were opposite to those of brain after str

133 trophy and interlelukin-6 gene expression in epididymal fat, along with the splenic proinflammatory p

134 quantified by magnetic resonance imaging and epididymal fat-pad weights.

135 dexamethasone prevented ATM accumulation in epididymal fat.

136 ependent and PPARalpha-independent manner in epididymal fat.

137 neal fat, but was without effect on GLUT4 in epididymal fat.

138 receptor type in islets, liver, kidney, and epididymal fat.

139 a, and an enhanced proinflammatory status of epididymal fat.

140 ce also exhibit adipocyte hypertrophy in the epididymal fat.

141 sion of Egr1 while decreasing ATGL levels in epididymal fat.

142 showed significantly reduced body weight and epididymal fat.

143 oliferator-activated receptor (PPAR)gamma in epididymal fat; enzymes of fatty acid oxidation and thei

144 -induced glucose uptake in soleus muscle and epididymal fat; insulin inhibition of lipolysis was also

145 white adipose tissues including inguinal and epididymal fats and also in brown adipose tissue but not

146 Detection of epididymal flow is infrequent in postpubertal patients b

147 With current ultrasound imaging technology, epididymal flow was demonstrated not only in the head bu

148 Testicular and epididymal flow were analyzed retrospectively in 24 test

149 Examination of the epididymal fluid and spermatozoa from L68Q mice showed i

150 r these studies suggest that amyloids in the epididymal fluid can be cytotoxic to the maturing sperma

151 The addition of epididymal fluid from L68Q mice to WT spermatozoa result

152 ty compared with WT spermatozoa incubated in epididymal fluid from WT mice.

153 L68Q epididymal fluid that was depleted of cystatin C amyloid

154 both the maintenance of spermatogenesis and epididymal function and it further suggests that BMP8 an

155 mis, the role of Bmp7 in spermatogenesis and epididymal function cannot be revealed by simply examini

156 gate the role of Bmp7 in spermatogenesis and epididymal function.

157 ting a novel role for BMPs in the control of epididymal function.

158 , we studied the role of RNA interference in epididymal functions.

159 I from sperm results in an inability to bind epididymal glycoconjugates that normally maintain sperm

160 Rat androgen-regulated acidic epididymal glycoprotein (AEG), also known as Protein DE,

161 spermatocytes to Seritoli cells, and acidic epididymal glycoproteins that bind to sperm and have bee

162 aceptive approach frequently associated with epididymal granuloma and sperm autoantibody formation.

163 The mean resistive indexes for the right epididymal head, body, and tail were 0.55, 0.55, and 0.5

164 of mouse adipose cell-size distributions in epididymal, inguinal, retroperitoneal, and mesenteric fa

165 ts in spermatogenesis and in maintaining the epididymal integrity of the caput and caudal regions.

166 sions consisted of scrotal wall liposarcoma, epididymal leiomyosarcoma, and recurrent spindle cell ma

167 Epididymal leptin mRNA measured by Northern blot analysi

168 ervation of a cluster of five genes encoding epididymal lipocalins, differently regulated and regiona

169 Protein DE is secreted into the epididymal lumen and binds to sperm heads during their t

170 endogenous transglutaminase activity in the epididymal lumen catalyzed the formation of SDS-resistan

171 ropose that transglutaminase activity in the epididymal lumen may function as a mechanism of extracel

172 ing CRES are a component of the normal mouse epididymal lumen without any apparent cytotoxic effects

173 RES amyloid may also form in vivo within the epididymal lumen.

174 he appearance of numerous round cells in the epididymal lumen.

175 RES has the potential to form amyloid in the epididymal lumen.

176 , but not the viable, spermatozoa within the epididymal lumen.

177 ility of sperm and a significant increase in epididymal luminal Ca(2+) concentration that is mirrored

178 in abnormally high Ca(2+) concentrations in epididymal luminal fluid and in a dramatic but incomplet

179 he presence of multiple forms of CRES in the epididymal luminal fluid, including SDS-sensitive and SD

180 cessing of mouse fertilin beta occurs during epididymal maturation and involves changes in the cytopl

181 rement for sAC during spermatogenesis and/or epididymal maturation and reveal limitations inherent in

182 of sperm functionality is due to problems in epididymal maturation or to the absence of cSrc in sperm

183 After epididymal maturation, sperm capacitation, which encompa

184 is protein is acquired by sperm later during epididymal maturation.

185 succination of protein is also increased in epididymal, mesenteric, and subcutaneous adipose tissue

186 ng the literature's current understanding of epididymal morphogenesis, we will highlight some of the

187 te in this report that capacitation of cauda epididymal mouse sperm in vitro was accompanied by a tim

188 ion with contralateral testicular atrophy or epididymal obstruction.

189 eptin had no effect on leptin mRNA in either epididymal or retroperitoneal white adipose tissue (WAT)

190 trated into the posterior head domain during epididymal passage.

191 mutant mice, however, unlike in the testes, epididymal Pem expression required germ-cell-induced fac

192 Epididymal, perirenal, and inguinal WAT weighed 139-185%

193 by RT-PCR in the mouse WAT depots examined (epididymal, perirenal, s.c., and mammary gland) and in i

194 ghly expressed in s.c. preadipocytes than in epididymal preadipocytes.

195 ATP release was detected from the mouse epididymal principal cell line (DC2) and increased by ad

196 n human chromosome 20q 12-13.2 called Eppin (Epididymal protease inhibitor) that expresses three mRNA

197 s report we describe the discovery of Eppin (Epididymal protease inhibitor), a gene on human chromoso

198 known genes: two L1 repeat genes and rabbit epididymal protein 52.

199 b and contains nine exons encoding an 1120bp epididymal Protein DE mRNA.

200 el gene Rnase10 encoding a secreted proximal epididymal protein in the mouse results in a binding def

201 nalysis using PSG2 showed that certain sperm/epididymal proteins are undersulfated in Tpst2(-/-) mice

202 A phylogenetic analysis of the new epididymal proteins reveals their spread position in the

203 ke into adipose cells, we incubated isolated epididymal rat adipocytes with the globular domain of re

204 Microsurgical techniques for vasal-epididymal reconstruction and sperm retrieval have been

205 The fold of NGAL is most similar to the epididymal retinoic acid-binding protein, another lipoca

206 increased UCP-2 mRNA by more than 10-fold in epididymal, retroperitoneal, and subcutaneous fat tissue

207 oma, spermatic cord injury or contusion, and epididymal, scrotal, and urethral injuries.

208 Selective overexpression of Human epididymal secretory protein E4 (HE4) points to a role i

209 regulation of CAII and CAIV in the different epididymal sections of the knockout lines.

210 cted lateral mobility in both testicular and epididymal sperm (D < 10(-10) cm(2)/s).

211 ) or ADAM3 (cyritestin) are infertile; cauda epididymal sperm (mature sperm) from these mutant mice c

212 localized to the apical segment of the cauda epididymal sperm acrosome.

213 n, as well as percutaneous and microsurgical epididymal sperm aspiration.

214 ugh meiosis and spermiogenesis and generated epididymal sperm at approximately 50% of control levels,

215 e Jackson Laboratory are infertile, have low epididymal sperm concentrations, and produce sperm with

216 Normal epididymal sperm count, spermatozoa morphology, capacita

217 ificant reductions in serum testosterone and epididymal sperm count.

218 Diets that optimized testes mass and epididymal sperm counts (indicators of gamete production

219 e was almost normal, with testis weights and epididymal sperm counts being unaffected.

220 sterile and show reduced sperm motility and epididymal sperm counts.

221 wo types of voltage-gated Ca(2+) channels in epididymal sperm examined prior to capacitation.

222 Mutant epididymal sperm exhibit diminished motility.

223 Mutant epididymal sperm exhibited abnormal morphology, includin

224 Despite their sterility, some epididymal sperm from Tenr mutants have normal morpholog

225 Epididymal sperm from Tnp2-null mice showed an increase

226 gellar waveform analysis show that for mouse epididymal sperm in vitro, the resting flagellar beat fr

227 The addition of S-Ht31 to bovine caudal epididymal sperm inhibits motility in a time- and concen

228 suggest an essential role of this kinase in epididymal sperm maturation involving cSrc extracellular

229 During epididymal sperm maturation, the lipid content of the sp

230 e processing pattern observed in vivo during epididymal sperm maturation.

231 Moreover, epididymal sperm numbers were not affected in FABP9(-/-)

232 rincipal piece in testicular sperm, while in epididymal sperm p109 and p26 were present only in the p

233 Alkaline phosphatase treatment of epididymal sperm proteins demonstrated that p109 was a p

234 The pHi of mouse cauda epididymal sperm was determined from the fluorescence ex

235 d in the tail and acrosomal regions of mouse epididymal sperm, while TSSK2 was found in the equatoria

236 physiological membrane potentials in corpus epididymal sperm.

237 2 is a key element for stability of ADAM3 in epididymal sperm.

238 9.6% versus 33.2% +/- 7.5% (P = 0.0104) for epididymal sperm.

239 of structural head abnormalities in residual epididymal sperm.

240 ds, but condensation was still incomplete in epididymal sperm.

241 nd cauda epididymis, but on only 6% of caput epididymal sperm.

242 ro" domain of the precursor) were present in epididymal sperm.

243 o-AKAP82 in condensing spermatids but not in epididymal sperm.

244 ibrous sheath preparations isolated from rat epididymal sperm.

245 CRES (cystatin-related epididymal spermatogenic), a member of the cystatin supe

246 e epididymal cystatin CRES (cystatin-related epididymal spermatogenic), cst8, a reproductive-specific

247 n vitro fertilization (IVF) that failed with epididymal spermatozoa alone.

248 etylneuraminic acid residues was detected in epididymal spermatozoa and epithelial cells using combin

249 tigate whether alterations of the sialome of epididymal spermatozoa and surrounding epithelial cells

250 ive form of pig zonadhesin from capacitated, epididymal spermatozoa comprises two covalently associat

251 rain, heart, liver, lung, and muscle, and in epididymal spermatozoa from adult mice.

252 In vitro studies showed that epididymal spermatozoa from L68Q mice were unable to fer

253 nuclear envelope and cytoplasmic droplet of epididymal spermatozoa.

254 of incompletely processed forms remained in epididymal spermatozoa.

255 iece of the flagellum between testicular and epididymal spermatozoa.

256 as localized to the principal piece of mouse epididymal spermatozoa; (2) mouse CABYR has two coding r

257 while the proximal centriole is lost during epididymal stage.

258 e tissues including perivascular, perirenal, epididymal, subcutaneous and brown adipose tissue.

259 hite and brown adipose depots were examined (epididymal, subcutaneous, perirenal, and interscapular).

260 3)H]NE turnover in IBAT, but increased it in epididymal, though not retroperitoneal, fat.

261 Changes that occur to mammalian sperm upon epididymal transit and maturation render these cells cap

262 osomes (vesicles that fuse with sperm during epididymal transit) carry RNA payloads matching those of

263 During the epididymal transit, polySia carriers were partially inte

264 dual loss of ADAM3 and ADAM6 proteins during epididymal transit.

265 on at multiple levels, enhances lipolysis in epididymal WAT (eWAT) because of the upregulation of gen

266 lerance, reduced insulin signaling in liver, epididymal WAT and heart, and downregulation of oxidativ

267 1 and fatty acid synthase protein levels in epididymal WAT of HFD-fed rats.

268 ght gain (as well as plasma lipid levels and epididymal WAT sizes in HFD-fed rats).

269 sis of intra-abdominal white adipose tissue (epididymal WAT) showed elevated expression of mRNA and p

270 regulated lipolysis and lipogenesis genes in epididymal WAT.

271 t, show no difference in the growth of their epididymal white adipose tissue (epiWAT) but they show e

272 Hepatic lipids extracted from mouse liver, epididymal white adipose tissue (eWAT) and subcutaneous

273 c mice overexpressing Tnmd develop increased epididymal white adipose tissue (eWAT) mass, and preadip

274 pase (HSL) in cultured adipocytes and in the epididymal white adipose tissue (EWAT) of C57BL/6 mice.

275 ucturally distinct PPARgamma agonists in the epididymal white adipose tissue (EWAT) of db/db mice, 33

276 In epididymal white adipose tissue (eWAT) of PDE3B KO mice

277 increased insulin singling in both liver and epididymal white adipose tissue (eWAT).

278 nd 12.4%, respectively, in the perirenal and epididymal white adipose tissue (PWAT, EWAT) compared to

279 DUSP5, an ERK1/2 phosphatase, was induced in epididymal white adipose tissue (WAT) in response to die

280 thesis leads to inhibition of lipogenesis in epididymal white adipose tissue (WAT), induction of brow

281 naling in liver and visceral adipose tissue (epididymal white adipose tissue [WAT]), reduced WAT infl

282 ch in depot utilisation from subcutaneous to epididymal white adipose tissue was associated with a wo

283 and enhanced MPO expression and activity in epididymal white adipose tissue, with an increase in bod

284 Epididymal white fat cells from cavin-1-null mice were s

285 through multisynaptic pathways to liver and epididymal white fat in mice using pseudorabies virus st

286 ment resulted in a decrease in abdominal and epididymal white fat pad weights, while interscapular br

287 ose (2-DG) uptake by the retroperitoneal and epididymal white tissue and IBAT, but skeletal muscle 2-