• 한국식품영양과학회지
• /
• 제42권4호
• /
• pp.587-594
• /
• 2013

생약재(백복령, 사인 및 창출) 추출물을 동량으로 혼합한 것에 와송 추출물을 첨가하여 만든 복합물이 당뇨쥐의 혈당강하 및 혈중 지질 성분 변화에 미치는 영향을 실험하였다. 정상군, 당뇨 대조군, 생약재 혼합물 급여군(D-MH), 생약재 혼합물과 와송 추출물의 1:1 복합물 급여군(D-MHOA) 및 1:3 복합물 급여군(D-MHOB)으로 구분하여 4주간 실험 사육하였다. 실험 사육 4주 후 체중의 증가량은 모든 실험군이 당뇨 대조군에 비해 증가되었으나, D-MHOB군에서만 유의적인 증가를 보였다. 실험 사육 기간 동안 공복 혈당은 실험 식이의 급여 2주 후부터 모든 실험군에서 대조군에 비해 유의적인 감소를 보였으며, 2~3주 동안에는 D-MH군과 D-MHOA군 간에 비슷한 수준이었다. 4주 후에는 D-MHOB군의 공복 혈당이 가장 낮았다. 내당능 측정 결과, 포도당 급여 60분에 모든 실험군에서 최고 혈당치를 보였으나, 생약재 혼합물 및 와송의 복합물 급여군이 대조군에 비해 유의적으로 개선되었다. 당화 헤모글로빈 함량은 정상군(3.9%)에 비해 대조군이 약 1.9배 증가되었으며, D-MH군에 비해 D-MHOA 및 D-MHOB군에서 유의적으로 감소되었다. 생약재에 대한 와송의 첨가량이 많을수록 혈청 총 지질 및 총 콜레스테롤 함량은 대조군에 비해 유의적으로 감소되었으나, HDL-C 함량은 D-MHOB군이 대조군에 비해 유의적으로 높았다. GPT 활성은 D-MHOB군이 여타의 실험군에 비해 유의적으로 낮았다. 생약재 혼합물 급여군에 비해서 와송 추출물의 첨가군에서 지질과산화물 함량은 감소되었으나 와송의 첨가량에 따른 유의차는 작았다. 항산화 활성은 와송의 첨가량에 따라 유의적으로 증가하였다. 따라서 와송은 생약재 혼합물에 첨가됨으로써 혈당 저하 및 지질 개선 효과를 증가시키는 것으로 확인되었다.

• 한국식품영양과학회지
• /
• 제34권7호
• /
• pp.973-979
• /
• 2005

한국에서 자생하는 흑송의 솔잎을 재료로 하여 항당뇨효능에 대한 생리 활성을 규명하고자 STZ로 당뇨를 유발시킨 흰쥐 에 솔잎증류액을 15일간 복강투여 후 체중, 혈당, OGTT, 혈액성분에 미치는 영향 및 간과 췌장의 조직병리학적 변화를 관찰하였다. 솔잎 투여군의 체중은 솔잎투여 6일째에 잠시 체중의 상승이 나타났을 뿐 그 이후에는 DM군에서와 같이 체중의 증가를 보이지 않았다. 공복혈당은 DM군에 비해 솔잎투여군에서 용량효과적으로 낮아지는 경향을 보였으며 15일째에 HP군에서 NC군의 수준으로 근접하였다. 구강내당능 검사결과 혈당곡선은 DM군에 비해 통계적 유의성은 없었으나 솔잎투여군에서 투여용량에 따라 감소경향을 보였다. 간기능관련지수로서 혈장내 total protein, albumin, AST는 솔잎투여에 따른 변화가 없었고, ALP와 ALT는 솔잎투여군 모두에서 DM군에 비해 감소하는 경향을 나타내었다. 신장기능 관련지수에서는 creatinine, uric acid, calcium, IP는 개선 경향이 관찰되지 않았으나, BUN에서는 DM과 비교시 솔잎투여군 모두에서 용량효과적으로 개선되는 경향을 보였다. 지질대사관련지수로서 total cholesterol, TG, HDL-C, LDL-C 농도는 모든 실험군간에 유의적인 차이를 보이지 않았다. 간 조직과 췌장조직 병리학적 관찰결과 간조직의 경우 DM군과 솔잎투여군의 일부에서 염증세포의 침윤이 부분적으로 관찰되었고 췌도세포에서는 DM군은 췌장실질의 괴사, 출혈성 병변, 지방세포의 괴사가 관찰되었으나 솔잎투여군 모두에서 DM군에 비해 억제되는 현상을 관찰할 수 있었다. 결론적으로 솔잎추출물 투여 에 의 괘 공복혈당이 낮아지고 당내성이 높아지는 경향을 보였고 간기능 지표 중 ALP와 ALT, 신장기능지표 중 BUN만이 솔잎 투여에 의한 개선효과를 나타내었으며, 혈중 지질 개선효과는 나타내지 않았다.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
• /
• 제36권5호
• /
• pp.392-401
• /
• 2010

Introduction: Diabetes mellitus, as a major health problem for the elderly has been shown to alter the properties of the bone and impair bone healing around a titanium implant in both humans and animals. The aim of this study was to examine the effect of adipose-derived stem cells on the healing process around a titanium implant in streptozotocin-induced diabetic rats. Materials and Methods: Thirteen rats were divided into two groups: adipose-derived stem cells injected group and a control group. A titanium screw implant (diameter: 2.0 mm, length: 3.5 mm) was placed into both tibia of 13 rats: 13 right tibia as the control group and 13 left tibia as the experimental group. The rats were sacrificed at different intervals (1, 2, and 4 weeks) after implantation for histopathology observations and immunohistochemistric analysis. Results: The histopathological findings revealed earlier new formed bone in the experimental group than the control group. In particular, at 1 week after implantation, the experimental group showed more newly formed bone and collagen around the implant than the control group. In immunohistochemistric analysis, osteoprotegerin (OPG) expression in the experimental group increased early compared to that of the control group until 2 weeks after implantation. However, after 2 weeks, OPG expression in the experimental group was similar to OPG expression in the control group. The receptor activator of nuclear factor ${\kappa}B$ ligand (RANKL) expression in the experimental group increased early compared to that of the control group, and then decreased at 2 weeks. After 2 weeks, the level of RANKL expression was similar in both groups. Conclusion: These results suggest that adipose-derived stem cells in implantation can promote bone healing around titanium, particularly in diabetes mellitus induced animals.

• Reproductive and Developmental Biology
• /
• 제33권3호
• /
• pp.163-169
• /
• 2009

Many biological systems are regulated by an intricate set of feedback loops that oscillate with a circadian rhythm of roughly 24 h. This circadian clock mediates an increase in body temperature, heart rate, blood pressure, and cortisol secretion early in the day. Recent studies have shown changes in the amplitude of the circadian clock in the hearts and livers of streptozotocin (STZ)-treated rats. It is therefore important to examine the relationships between circadian clock genes and growth factors and their effects on diabetic phenomena in animal models as well as in human patients. In this study, we sought to determine whether diurnal variation in organ development and the regulation of metabolism, including growth and development during the juvenile period in rats, exists as a mechanism for anticipating and responding to the environment. Also, we examined the relationship between changes in growth factor expression in the liver and clock-controlled protein synthesis and turnover, which are important in cellular growth. Specifically, we assessed the expression patterns of several clock genes, including Per1, Per2, Clock, Bmal1, Cry1 and Cry2 and growth factors such as insulin-like growth factor (IGF)-1 and -2 and transforming growth factor (TGF)-${\beta}1$ in rats with STZ-induced diabetes. Growth factor and clock gene expression in the liver at 1 week post-induction was clearly increased compared to the level in control rats. In contrast, the expression patterns of the genes were similar to those observed after 5 weeks in the STZ-treated rats. The increase in gene expression is likely a compensatory change in response to the obstruction of insulin function during the initial phase of induction. However, as the period of induction was extended, the expression of the compensatory genes decreased to the control level. This is likely the result of decreased insulin secretion due to the destruction of beta cells in the pancreas by STZ.

• Anatomy and Cell Biology
• /
• 제57권3호
• /
• pp.446-458
• /
• 2024

The study aims to compare the action of Pleurotus cornucopiae and glibenclamide on alloxan-induced diabetes and ascertain how an aqueous extract of the edible mushroom regulates the expression of nuclear factor erythroid 2-related factor 2 (Nrf2), oxidative stress biomarkers and renal toxicity in a diabetic male Wistar rat model. Twenty-five adult male Wistar rats were randomly grouped into five groups with five rats per. Group 1 and those in the treatment groups received normal feed and water ad libitum. Group 2 received intraperitoneal administration of alloxan monohydrate (150 mg/kg body weight). Group 3 received alloxan monohydrate and glibenclamide (5 mg/kg body weight bwt), group 4 received alloxan monohydrate plus the extract (250 mg/kg bwt) and group 5 received alloxan monohydrate plus the extract (500 mg/kg bwt). The administration of glibenclamide plus the extract was oral for 14 days. Glibenclamide and the extract lowered blood glucose level, catalase, and glutathione peroxidase activities, increased the superoxide dismutase (SOD) activity in rats with alloxan induced diabetes. The extract at 500 mg/kg bwt reduced the plasma urea and sodium concentration in the treated rats. The extract and glibenclamide could detoxify alloxan and restore its induced renal degeneration and glomeruli atrophy, intra renal hemorrhage and inflammation and oxidative biomarkers through activation of Nrf2 expression. The drug glibenclamide and P. cornucopiae have appreciable hypoglycemic activity and potential to restore the normal renal architecture in the rats, hence they offer similar curative effects. Additionally, the extract at 500 mg/kg bwt activated SOD and Nrf2 expression more than glibenclamide in rats with alloxan-induced diabetes.

• Nutrition Research and Practice
• /
• 제18권5호
• /
• pp.633-646
• /
• 2024

BACKGROUND/OBJECTIVES: Cladophora glomerata extract (CGE), rich in polyphenols, was reported to exhibit antidiabetic and renoprotective effects by modulating the functions of protein kinases-mediated organic anion transporter 1 (Oat1) and 3 (Oat3) in rats with type 2 diabetes mellitus (T2DM). Nevertheless, the antioxidant effects of CGE on such renoprotection have not been investigated. This study examined the mechanisms involved in the antioxidant effects of CGE on renal organic anion transport function in an in vivo study. MATERIALS/METHODS: Diabetes was induced in the rats through a high-fat diet combined with a single dose of 40 mg/kg body weight (BW) streptozotocin. Subsequently, normal-diet rats were supplemented with a vehicle or 1,000 mg/kg BW of CGE, while T2DM rats were supplemented with a vehicle, CGE, or 200 mg/kg BW of vitamin C for 12 weeks. The study evaluated the general characteristics of T2DM and renal oxidative stress markers. The renal organic transport function was assessed by measuring the para-aminohippurate (PAH) uptake using renal cortical slices and renal inflammatory cytokine expression in the normal diet (ND) and ND + CGE treated groups. RESULTS: CGE supplementation significantly reduced hyperglycemia, hypertriglyceridemia, insulin resistance, and renal lipid peroxidation in T2DM rats. This was accompanied by the normalization of high expressions of renal glutathione peroxidase and nuclear factor kappa B by CGE and vitamin C. The renal anti-inflammation of CGE was evidenced by the reduction of tumor necrosis factor-1α and interleukin-1β. CGE directly blunted sodium nitroprusside-induced renal oxidative/nitrosative stresses and mediated the PAH uptake in the normally treated CGE in rats was particularly noteworthy. These data also correlated with reduced nitric oxide production, highlighting the potential of CGE as a therapeutic agent for managing T2DM-related renal complications. CONCLUSION: These findings suggest that CGE has antidiabetic effects and directly prevents diabetic nephropathy through oxidative/nitrosative stress pathways.

• Nutrition Research and Practice
• /
• 제5권3호
• /
• pp.205-213
• /
• 2011

Exercise training (ET) and selenium (SEL) were evaluated either individually or in combination (COMBI) for their effects on expression of glucose (AMPK, PGC- $1{\alpha}$, GLUT-4) and lactate metabolic proteins (LDH, MCT-1, MCT-4, COX-IV) in heart and skeletal muscles in a rodent model (Goto-Kakisaki, GK) of diabetes. Forty GK rats either remained sedentary (SED), performed ET, received SEL, ($5\;{\mu}mol{\cdot}kg$ body $wt^{-1}{\cdot}day^{-1}$) or underwent both ET and SEL treatment for 6 wk. ET alone, SEL alone, or COMBI resulted in a significant lowering of lactate, glucose, and insulin levels as well as a reduction in HOMA-IR and AUC for glucose relative to SED. Additionally, ET alone, SEL alone, or COMBI increased glycogen content and citrate synthase (CS) activities in liver and muscles. However, their effects on glycogen content and CS activity were tissue-specific. In particular, ET alone, SEL alone, or COMBI induced upregulation of glucose (AMPK, PGC-la, GLUT-4) and lactate (LDH, MCT-1, MCT-4, COX-IV) metabolic proteins relative to SED. However, their effects on glucose and lactate metabolic proteins also appeared to be tissue-specific. It seemed that glucose and lactate metabolic protein expression was not further enhanced with COMBI compared to that of ET alone or SEL alone. These data suggest that ET alone or SEL alone or COMBI represent a practical strategy for ameliorating aberrant expression of glucose and lactate metabolic proteins in diabetic GK rats.

• 대한한방내과학회지
• /
• 제27권4호
• /
• pp.791-797
• /
• 2006

Objectives : The objective of the study was to observe the effects of different treatment lengths of Rhizoma Alismatis on diabetes mellitus. Methods : Rats were divided into three groups: normal(non-treated group), control (group administered saline for 4, 11, and 18 days), and RA (group administered 2.45mg/200g Rhizoma Alismatis for 4, 11, and 18 days). The experimental results were derived from the measurement of the levels of glucose, ALP, AST, ALT, creatinine and BUN in the serum from the rats on days 4, 11, and 18. Results : The glucose level in the serum significantly decreased on the 18th day. The ALP level in the serum did not show statistical significance. The GOT and GPT levels in the serum slightly decreased on the 4th, 11th, and 18th days, but did not show statistical significance. The creatinine level in the serum was unchanged for all of them. The BUN level in the serum did not show statistical significance. Conclusions : According to the above results, it is concluded that Rhizoma Alismatis has a therapeutic effect on diabetes mellitus with a longer period ofintake. As to influence upon the liver and kidney, there was no damage orside effects.

• 대한한의학회지
• /
• 제19권1호
• /
• pp.109-126
• /
• 1998

This experiment was performed in order to investigate the effect of Rosa rugosae Radix on hyperglycemia and diabetes in streptozotocin-induced rats. In this study, the experimental rats were divided into three groups: Control group, Group-A(Aqua-acupuncture group) and Group-B(Orally administ:ered group). Under the same condition, three groups were injected 50mg/kg of streptozotocin into abdomen for 3days. And then, Control group was administered water, Group-A was administered Rosa rugosae Radix aqua-acupuncture to S36, B20 and B21. Group-B was administered Rosa rugosae Radix water extract for 14days. Then kidney weight, serum glucose levels, BUN levels, creatinine levels and Langerhans islets were measured on 7th and 14th days. The obtained results are summarized as follows: 1. The kidney weight of control group was heavier than those of group-A and group-Bon 7th day. 2. The levels of serum glucose were decreased in group-A and group-B at l20minutes 14th day as compared with control group. 3. The levels of BUN were decreased in group-A and group-B as compared with control group. 4. In histological observations, Langerhans islets of control group showed disrupted or condensed nudei, and intercellular spaces between acini were enlarged. In the group-A and group-B, histological damages of the acini and Lagerhans islets were recovered as compared with control group. These results suggest that Rosa rugosae Radix can applied for the treatment of diabetes melitus.

• 한국식품영양과학회지
• /
• 제21권2호
• /
• pp.117-123
• /
• 1992

Nicotinamide의 항 당뇨작용을 연구할 목적으로 streptozotocin으로 당뇨병을 유발시킨 흰 쥐를 모델동물로 하여 수분섭취량과 체중, 혈당, 뇨당 및 혈중 in-sulin함량과 췌장중 효소변동을 형태학적인 측면과 함께 상호 비교 관찰하였다. Nicotinamide의 전처리로 STZ에 의해 유발되는 당뇨병시 나타나는 생리적 현상의 감소 및 혈당증가가 유의성있게 감소되었으며 혈중 insulin농도도 STZ에 의해 현저히 억제되던 것이 nice-tinamide의 전처리로 정상수준으로 회복되었다. 혈청중 lipase 및 trypsin활성은 STZ투여에 의해 증가되었으며, amylase활성은 대조군에 비해서 억제되었으나 nicotinamide의 전처리로 lipase, trypsin 및 amylase활성이 회복되었다. 췌장의 형태학적인 변화에서는 STZ 투여로 췌장소엽세포 및 췌관을 포함하는 외분비계의 조직에는 변화가 없으나 Langerhans's islet $\beta$세포가 심하게 파괴되었고 nicotinamide의 전처리로 $\beta$세포의 파괴가 현저하게 감소되었다.