• 농약과학회지
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• 제10권2호
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• pp.76-83
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• 2006

비선택성 제초제인 glufosinate-ammonium(ammonium 4-[hydroxy-(methyl)phosphinoyl]-DL-homoalaninate, GLA, 상표명 : 바스타 액제)의 비표적생물에 대한 영향을 알아보기 위하여 지렁이와 토양미생물 및 작물에 대한 영향시험을 수행하였으며, 시험토양 중 GLA 및 그 대사산물인 3-MPP의 잔류성을 시험하였다. 토양중 지렁이에 대한 영향시험 결과 GLA가 288 mg a.i. $m^{-2}$ 약량으로 처리된 토양 중 지렁이의 치사체는 관찰되지 않았으며, 약제처리 후 시험기간 동안 지렁이 생체 중 또한 무처리에서 $9.076{\pm}0.55$ g에 비해 토양 표면처리구는 $8.046{\pm}0.37$ g, 토양혼화처리에서 $8.349{\pm}0.785$ g 으로서 체중증가율에서 GLA의 영향은 없는 것으로 판단된다. 그리고 토양 미생물에 대한 영향시험 결과 진균, 세균 및 방선균의 균수는 무처리구에서 각각 $3.7{\times}10^4$, $3.7{\times}10^5$, $3.7{\times}10^4$이었으며 144 mg a.i $m^{-2}$의 약량으로 처리된 시험구에서 진균은 $6.2{\times}10^4$, 세균은 $1.5{\times}10^6$, 방선균은 $5.7{\times}10^4$으로 무처리구와 같이 약제처리 후 시간의 경과에 따른 미생물수의 변화정도가 큰 차이를 보이지 않았다. 또한 토양에 처리된 GLA와 3-MPP의 잔류분석결과 검출한계는 두 화합물 모두 0.02 mg $kg^{-1}$이었으며 반감기는 사질식양토에서 30일 간격으로 2회 처리 시 15일이었다. 한편 감자밭과 배추밭의 고랑에 GLA를 처리한 후 두 작물의 생엽 중 카로티노이드 등의 생리생화학적 성분은 손제초구를 100%로 하여 비교해 본 결과 감자에서 $90.00{\sim}104.33%$이었으며 배추에서는 $99.0{\sim}112.67%$로 약제처리구에서 두드러진 차이를 나타내지 않았다. 이상의 결과에서 GLA는 지렁이와 토양 미생물에 아무런 영향을 미치지 않았고 토양 중 반감기도 15일 이내로 토양 중에 노출 시 매우 신속하게 분해 소실되어 그 위해성은 매우 낮은 수준인 것으로 판단되며, 작물 재배지에서 밭고랑의 잡초 방제를 위해 비산방지 기구를 이용하여 살포할 경우에는 재배 작물에 안전한 것으로 판단되었다.

• The Korean Journal of Pain
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• 제13권1호
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• pp.8-18
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• 2000

Background: Intraperitoneal (IP) and intrathecal (IT) administration of $\alpha$-amino-3-hydroxy-5-methyl-4-isoxazole-propionic (AMPA) and kainate (KA) receptor antagonist attenuate hyperalgesia in various models of persistent pain. The purpose of this study was to assess the effects of IP and IT LY293558, a novel AMPA/KA receptor antagonist on mechanical hyperalgesia after incision. Methods: Sprague-Dawley rats were anesthetized with halothane and underwent plantar incision. Two hours later, responses to mechanical stimuli were assessed using the response frequency to a nonpunctate mechanical stimulus and withdrawal threshold to calibrated von Frey filaments. One group of rats received vehicle, 5 or 10 mg/kg of LY293558 IP. In the other group, vehicle, 0.2, 0.5 or 2 nmol of LY293558 was administered IT. Ataxia and motor function were also evaluated. Results: Hyperalgesia was persistent in both the vehicle and 5 mg/kg group. IP administration of 10 mg/kg of LY293558 increased withdrawal threshold at 30 and 60 min after incision; deficits in rotorod performance were observed at 30, 60, 90 and 150 min. IT administration of 0.5 nmol of LY293558 increased the median withdrawal threshold at 30 and 60 min. Motor function was only impaired at 30 min. IT administration of 2 nmol produced hemiparesis. Again, inhibition of pain behaviors outlasted the effects on motor function. Conclusions: These data further suggest AMPA/KA receptors are important for the maintenance of pain behaviors caused by incisions. IT administration of LY293558 was more effective than systemic administration and reducing pain behaviors caused by a surgical incision.

• Preventive Nutrition and Food Science
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• 제13권1호
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• pp.54-59
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• 2008

This study was conducted to investigate the effect of pH on the formation of furfural compounds from glucose and fructose reacting with amino acid enantiomers in the Maillard reaction. Hydroxymethylfurfural (HMF) content was highest at pH 4.0, and decreased with increasing pH. HMF was significantly higher in glucose-based systems than fructose-based systems. Furfuryl alcohol (FFA) and 5-methyl-2-furaldehyde (MF) were not increased with increasing pH, and only small amounts were formed. In addition, 2-furaldehyde (F) was found to increase in the systems, as pH increased. However, the content was small and variable. 2,5-Dimethyl-4-hydroxy-3(2H)-furanone (DMHF) was only found in Glc/D-Asn, Glc/L-Lys and Fru/D-Lys system, but the content was not increased with increasing pH. 2-acetylfuran (AF) was higher in Glc (or Fru)/L-Lys and Glc (or Fru)/D-Lys systems at pH 7.0. However, at pH 4.0, the content of AF was higher in the Glc (or Fru)/Gly and Glc (or Fru)/L-Asn systems. Therefore, this study aimed to observe the effect of pH, sugars and amino acid enantiomers on the production of furfural and related compounds by the Maillard reaction. A clear tendency was observed for some classes of compounds to be more easily formed at higher or lower pH. HMF was more readily formed at lower pH, while FFA, F, DMHF and MF were inhibited by acidic conditions. Particularly, compounds like FFA, F and MF were not affected by pH changes. In addition, DMHF and MF were only formed in L-Lys and D-Lys system.

• Asian-Australasian Journal of Animal Sciences
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• 제33권5호
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• pp.812-824
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• 2020

Objective: The aim of this work was to assess the effect of fermented blueberry (FB; 2%, 4%, and 6%) on the oxidative stability and volatile molecule profiles of emulsion-type sausage stored at 4℃ for 28 days. Methods: The antioxidant activity of FB was determined through radical-scavenging activity against 2, 2-diphenyl-1-picrylhydrazyl (DPPH) and hydroxyl radicals. Four formulations of sausage treatments with different FB levels (0%, 2%, 4%, 6%) were prepared, then peroxide value (POVs), thiobarbituric acid-reactive substances (TBARS) values, protein carbonyls and thiol groups were measured. The aroma profiles of sausages for each treatment was also determined. Results: The half maximal inhibitory concentration indicated that FB had greater scavenging ability than ascorbic acid against DPPH and hydroxyl radicals. Sausages with FB significantly retarded increases in POVs and TBARS, as well as in the content of protein carbonyls during all storage days (p<0.05). Particularly, 4% and 6% FB-treated sausages had better oxidation inhibition effects. However, FB accelerated the reduction in thiol groups (p<0.05). Additionally, FB inhibits the excessive formation of aldehyde compounds; for example, hexanal, which may cause rancid flavors, decreased from 58.25% to 19.41%. FB also created 6 alcohols (i.e., 2-methyl-1-propanol, 3-methyl-1-butanol, and phenylethyl alcohol), 5 ester compounds (i.e., ethyl acetate, ethyl lactate, and ethyl hexanoate) and 3-hydroxy-2-butanone in the sausages that contribute to sausage flavors. The principal component analysis showed that the aroma profiles of sausages with and without FB are easily identified. Conclusion: The addition of FB could significantly reduce the lipid and protein oxidation and improve oxidative stability for storage. Also, adding FB could inhibit rancid flavors and contribute to sausage flavors.

• Asian Pacific Journal of Cancer Prevention
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• 제16권16호
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• pp.7179-7188
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• 2015

Cancer is a major health obstacle around the world, with hepatocellular carcinoma (HCC) and colorectal cancer (CRC) as major causes of morbidity and mortality. Nowadays, there isgrowing interest in the therapeutic use of natural products for HCC and CRC, owing to the anticancer activity of their bioactive constituents. Boswellia serrata oleo gum resin has long been used in Ayurvedic and traditional Chinese medicine to alleviate a variety of health problems such as inflammatory and arthritic diseases. The current study aimed to identify and explore the in vitro anticancer effect of B. Serrata bioactive constituents on HepG2 and HCT 116 cell lines. Phytochemical analysis of volatile oils of B. Serrata oleo gum resin was carried out using gas chromatography-mass spectrometry (GC/MS). Oleo-gum-resin of B. Serrata was then successively extracted with petroleum ether (extract 1) and methanol (extract 2). Gas-liquid chromatography (GLC) analysis of the lipoidal matter was also performed. In addition, a methanol extract of B. Serrata oleo gum resin was phytochemically studied using column chromatography (CC) and thin layer chromatography (TLC) to obtain four fractions (I, II, III and IV). Sephadex columns were used to isolate ${\beta}$-boswellic acid and identification of the pure compound was done using UV, mass spectra, $^1H$ NMR and $^{13}C$ NMR analysis. Total extracts, fractions and volatile oils of B. Serrata oleo-gum resin were subsequently applied to HCC cells (HepG2 cell line) and CRC cells (HCT 116 cell line) to assess their cytotoxic effects. GLC analysis of the lipoidal matter resulted in identification of tricosane (75.32%) as a major compound with the presence of cholesterol, stigmasterol and ${\beta}$-sitosterol. Twenty two fatty acids were identified of which saturated fatty acids represented 25.6% and unsaturated fatty acids 74.4% of the total saponifiable fraction. GC/MS analysis of three chromatographic fractions (I,II and III) of B. Serrata oleo gum resin revealed the presence of pent-2-ene-1,4-dione, 2-methyl- levulinic acid methyl ester, 3,5- dimethyl- 1-hexane, methyl-1-methylpentadecanoate, 1,1- dimethoxy cyclohexane, 1-methoxy-4-(1-propenyl)benzene and 17a-hydroxy-17a-cyano, preg-4-en-3-one. GC/MS analysis of volatile oils of B. Serrata oleo gum resin revealed the presence of sabinene (19.11%), terpinen-4-ol (14.64%) and terpinyl acetate (13.01%) as major constituents. The anti-cancer effect of two extracts (1 and 2) and four fractions (I, II, III and IV) as well as volatile oils of B. Serrata oleo gum resin on HepG2 and HCT 116 cell lines was investigated using SRB assay. Regarding HepG2 cell line, extracts 1 and 2 elicited the most pronounced cytotoxic activity with $IC_{50}$ values equal 1.58 and $5.82{\mu}g/mL$ at 48 h, respectively which were comparable to doxorubicin with an $IC_{50}$ equal $4.68{\mu}g/mL$ at 48 h. With respect to HCT 116 cells, extracts 1 and 2 exhibited the most obvious cytotoxic effect; with $IC_{50}$ values equal 0.12 and $6.59{\mu}g/mL$ at 48 h, respectively which were comparable to 5-fluorouracil with an $IC_{50}$ equal $3.43{\mu}g/mL$ at 48 h. In conclusion, total extracts, fractions and volatile oils of B. Serrata oleo gum resin proved their usefulness as cytotoxic mediators against HepG2 and HCT 116 cell lines with different potentiality (extracts > fractions > volatile oil). In the two studied cell lines the cytotoxic acivity of each of extract 1 and 2 was comparable to doxorubicin and 5-fluorouracil, respectively. Extensive in vivo research is warranted to explore the precise molecular mechanisms of these bioactive natural products in cytotoxicity against HCC and CRC cells.

• 대한한의학회지
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• 제16권2호
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• pp.17-35
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• 1995

연구배경(硏究背景) 및 목적(目的): 국내(國內) 대부분(大部分)의 한방병원(韓方病院)에서 많은 수의 환자(患者)가 중풍(中風)으로 입원(入院)하고 있다. 이에 한방병원(韓方病院)을 찾고 있는 중풍환자(中風患者)에 대한 임상적(臨床的) 통계분석(統計分析)과 더불어 앞으로 나아가야 할 방향(方向)등에 대해 많은 연구(硏究)가 필요(必要)할 것으로 여겨져 본 연구(硏究)를 시작(始作)하였다. 대상(對象) 및 방법(方法): 1994년 1월(月) 1일(日)부터 동년(同年) 12월(月) 31일(日) 까지 경원대학교(暻園大學校) 부속(附屬) 한방병원(韓方病院) 순환기내과(循環器內科)에 Brain CT나 MRI상(上) 뇌혈관질환(腦血管疾患)으로 진단(診斷)받거나, 임상적(臨床的) 증상(症狀)으로 뇌졸중(腦卒中)으로 진단(診斷)받은 161예(例)의 환자(患者)를 대상(對象)으로 조사(調査)하였다. 결과(結果) 및 결론(結論): 1. 뇌졸중(腦卒中)의 종류별(種類別) 빈도(頻度)에서 뇌경색(腦梗塞)이 가장 많았으며 뇌출혈(腦出血), 지주막하출혈(蜘蛛膜下出血), 고혈압성뇌증(高血壓性腦症), 일과성뇌허혈발작(一過性腦虛血發作)의 순(順)이었다. 2. 선행질환(先行疾患)은 고혈압(高血壓)이 가장 많았으며, 당뇨(糖尿)도 많은 예(例)에서 나타났다. 3. 일반적(一般的)인 통례(通例)와는 달리 겨울보다는 여름에 많이 발생(發生), 입원(入院)하였다. 4. 입원당시(入院當時) 의식상태(意識狀態)가 안 좋았던 환자(患者)에게서 예후불량(豫後不良)한 환자(患者)가 많이 나타났다. 5. 물리치료(物理治療)의 평균(平均) 개시시기(開始時期)는 뇌경색(腦梗塞)에서 11.4일(日), 뇌출혈(腦出血)에서 22.7일(日)이었다. 6. 한(韓), 양방(洋方) 협진(協診)을 실시(實施)한 경우가 많았으며, 그 필요성(必要性)이 많이 나타났다.진단(診斷)에서부터 치료(治療)의 전과정(全過程)을 통(通)해서 서의치료(西醫治療)와 동의치료(東醫治療)를 결합(結合)하여 종합치료(綜合治療)를 하므로써 폐암(肺癌)의 치료효과(治療效果)를 높일 수 있는 새로운 치료법(治療法)으로 계속적인 연구(硏究)가 필요(必要)할 것으로 사료(思料)된다.較)하였다. 끝으로 본(本) 연구는 1965 年度 서울대학교 대학원(大學院) 연구비(硏究費)로 수행(遂行)한 것이며 본 연구를 시종 지도편달(指導鞭撻) 해 주신 서울대학교 농과대학 농화학과 주임교수 이춘영박사(李春寧博士)에게 감사(感謝)를 드리며 또한 본 연구의 시료를 제공하여 주신 서울대학교 농과대학 농학과 이고웅박사(李股雄博士)에 게 사의(謝意)를 표하는 동시에 본 연구의 분석에 협력하여 준 서울대학교 대학원 농화학과 김수영군(金洙榮君)에게 사의(謝意)를 표하는 바이다. 5 참조(參照)) (4) 벼를 pot에 심고 2회(回)에 걸쳐 control, Imidan, N-hydroxy methyl phthalimide, anthranilic acid 및 phthalimide의 10, 25, 50, 100 ppm 농도(濃度)의 각(各) 유제(乳劑)를 살포하고 일정기간후(一定期間後) 생육상(生育相)을 조사(調査)하였더니 Imidan 구(區)와 N-hydroxy methyl phthalimide 구(區)가 control 보다 좋은 성적(成績)을 보였다. (5) Imidan 250 ppm 유제(乳劑)를 수도엽면(水稻葉面)에 살포(撒布)하고 3 일(日), 5 일(日), 7 일(日) 및 14일후(日後)에 일정량(一定量)의 엽경(葉莖)을 채취(採取)하여 acetone으로 추출(抽出)k고 acetonitrile을 가지고 prechromatographic piriication 을 거쳐 paper chromatography에 의(依)하여 다음과

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1998년도 Proceedings of UNESCO-internetwork Cooperative Regional Seminar and Workshop on Bioassay Guided Isolation of Bioactive Substances from Natural Products and Microbial Products
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• pp.170-170
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• 1998

In order to discover new types of 5-hydroxytryptamine antagonists, we have devoted our attention to investigating naturally occurring compounds having anti-5HT activity in vitro. Recently, ${\gamma}$-mangostin [1,3,6,7-tetrahydroxy-2,8-bis(3-methyl-2-bytenyl)-9H-xanthen-9-one] from the fruit hull of Garcinia mangostana Linn has been shown to be a selective antagonist for 5-hydroxytryptamine$_{2A}$ receptors in smooth muscle and platelets. It is of interesting that y-mangostin which does not have a nitrogen atom, possesses marked 5-$HT_{2A}$ receptor blocking activity. The present study was undertaken to investigate the effects of ${\gamma}$-mangostin on central 5-HT receptors by using animal behavioural models. Intracerebronventricular injection of ${\gamma}$-mangostin (10-40n mol/mouse) inhibited 5-fluoro-${\alpha}$-methyltryptamin (5-FMT) (45 mg kg$^{-1}$, i.p.)-induced head-twitch response in mice in the presence or absence of citalopram (5-HT-uptake inhibitor). Neither the 5-FMT- nor the 8-hydroxy-2-( di-n-propylamino )tetralin (5-HT$_{1A}$-agonist)-induced 5-HT syndrome (head weaving and hindlimb abduction) was affected by ${\gamma}$-mangostin. The locomotor activity stimulated by 5-FMT through the activation of at-adrenoceptors did not alter in the presence of ${\gamma}$-mangostin. 5-HT-induced inositol phosphates accumulation in mouse brain slices was abolished by ketanserin. ${\gamma}$-Mangostin caused a concentration-dependent inhibition of the inositol phosphates accumulation and the binding of [$^3H$]-spiperone, a specific 5-$HT_{2A}$ receptor antagonist, to mouse brain membranes. Kinetic analysis of the [$^H3$]-spiperone binding revealed that ${\gamma}$-mangostin increased the $_{d}$ value without affecting the $B_{max}$ value, indicating the mode of the competitive nature of the inhibition by ${\gamma}$-mangostin. These results suggest that ${\gamma}$-mangostin inhibits 5-FMT-induced head-twitch response in mice by blocking 5-$HT_{2A}$ receptors not by blocking the release of 5-HT from the central neurone. ${\gamma}$-Mangostin is a promising 5-$HT_{2A}$ receptors antagonist in the central nervous system.m.

• 한국수의병리학회지
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• 제2권2호
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• pp.73-84
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• 1998

This study was carried out to investigate on the serum chemistry and the DNA ploidy changes in carcinogenesis of the rat liver and kidney. Sixty male Sprague-Dawley rats were divided into two groups. Group I was non-treated control. Group II was given initiators (2,2'-dihydroxy- di-N-propylnitrosamine, 0.1% in drinking water(d.w.) for 1 week and N-ethyl-N-hydroxy-ethylnitrosamine; 0.15% in d.w. for 1 week) and promoters (3'methyl-cholanthrene; 3'MC, l0mg/kg, intraperitoneally(i.p.) twice a week and DL-serine; 0.05% in d.w. for 5 weeks, from 3 to 8 weeks). All examinations were performed at 12 and 20 weeks RBC, HGBCp＜0.05) and PCVCp＜0.01) significantly decreased in Group II at 20 weeks. Activities of ALT, AST(p＜0.05) and GGT(p＜0.01) were significantly increased in Group II at 20 weeks. Flow cytometric analysis showed hepatocyte nuclei from normal livers were predominantly tetraploid(66~67%) and then diploid(28~30%). Most of hepatocyte nuclei from carcinogen-treated rats were diploid (52~68%) and less were tetraploid(28~42%). Neoplastic liver nodules and hepatocellular carcinoma contained almost exclusively diploid nuclei. Renal cell nuclei from normal kidney were predominantly diploid(88~93%), those from carcinogen-treated rats had an abnormal DNA-content peak(aneuploidy, 6-7%), near the tetraploidy area. These results suggest that diploidy may be an effective screening marker of the liver carcinogenesis. Aneuploidy may be an useful marker in assessment of the experimental renal carcinogenesis.

• 한국환경농학회지
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• 제12권1호
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• pp.27-34
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• 1993

Dimepiperate 및 그 주요(主要) 대사산물(代謝産物)인 dimepiperate-OH의 지표수(地表水)및 침투수중(浸透水中)의 잔류량(殘留量)을 lysimeter를 사용(使用)하여 약제처리후(藥劑處理後) 63일간(日間)에 걸쳐 경시적(經時的)으로 조사(調査)하였다. Dimepiperate의 지표수중(地表水中) 농도(濃度)는 시용(施用) 1일후(日後)에 3.0Kg/10a시용구(施用區)에서 $851{\sim}897ppb$, 6kg/10a시용구(施用區)에서 $1.755{\sim}1.781ppb$이었고 그 후 경시적(經時的)으로 감소(減少)하여 35일이후(日以後)는 1ppb이하의 극미량(極微量)만이 63일(日)까지 지속되었다. 침투수중(浸透水中)에서 dimepiperate는 약제처리(藥劑處理) 45일(日)이후부터 1ppb이하의 미량(微量)만이 검출(檢出)되기 시작하여 약제처리(藥劑處理) 63일후(日後)까지 큰 변화없이 지속(持續)되었으며 지표수중(地表水中)의 검출량(檢出量)에 비(比)하여 거의 무시할 정도의 극미량(極微量)이었다. Dimepiperate의 주요(主要) 중간대사물(中間代謝物)인 dimepiperate-OH는 dimepiperate표면시용후(表面施用後)부터 지표수중(地表水中)에 검출(檢出)되었고 2일후(日後)에 최고치(最高値) (dimepiperate 3.0Kg/10a처리구(處理區) $88{\sim}159\;ppb$, 6.0Kg/10a처리구(處理區) $135{\sim}173\;ppb$)에 달(達)하였으나, 그후 점점 감소(減少)되었다. Dimepiperate-OH의 경시적(經時的)인 농도감소(濃度減少)는 dimepiperate의 그것과 동일(同一)한 경로(經路)였으나, 35DAT이후부터는 dimepiperate농도(1ppb 이하)보다 dimepiperate-OH농도(2ppb 이하)가 높았다. 침투수중(浸透水中) dimepiperate-OH의 검출(檢出)은 처리량(處理量), 벼이앙 유무(有無)에 따라 달랐으나. 처리(處理) 21일후(日後)부터 검출(檢出)되기 시작하였으며 그 농도(濃度)는 $0.5{\sim}11\;ppb$로 63DAT까지 비슷한 수준(水準)이었다.

• 한국식품영양과학회지
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• 제39권8호
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• pp.1179-1186
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• 2010

무말랭이 및 가압볶음 무말랭이 열수 추출물의 항산화 효과를 in vitro와 LLC-$PK_1$ cellular system에서 살펴보았다. 무말랭이 열수 추출물과 가압볶음 무말랭이 열수 추출물의 라디칼 소거능을 $IC_{50}$로 비교해 보았을 때 DPPH(646.70 vs $135.45\;{\mu}g/mL$), superoxide anion(896.10 vs $566.98\;{\mu}g/mL$) 및 hydroxyl radical(722.26 vs $531.84\;{\mu}g/mL$)에 대한 가압볶음 열수 추출물의 효과가 유의적으로 높은 것으로 나타났다(p<0.001). 이러한 유리기 소거효과는 LLC-PK1 cell에서 pyrogallol, SNP 및 SIN-1 처리로 superoxide, nitric oxide 및 peroxynitrite를 생성하여 산화스트레스를 유발한 다음 무말랭이 및 가압볶음 무말랭이 열수추출물을 첨가하였을때 농도 의존적으로 세포생존율이 증가하고, 과산화물 생성량이 감소하여 세포손상을 보호하는 효과가 관찰되었다. 가압볶음 무말랭이 열수 추출물의 산화손상에 대한 보호 효과는 무말랭이 열수추출물에 비해 모든 유리기에서 유의적으로 높았다(p<0.05). 이러한 무말랭이 열수추출물의 항산화효과는 무에 함유되어 있는 함황 물질, 유리아미노산, 배당체 등에 의한 것으로 생각되며 가압볶음 무말랭이 열수 추출물의 효과가 더 높은 이유는 무말랭이에 함유된 유효성분이가압볶음에 의해 증가되고 더불어 볶음과정 중에서 생성된 maillard 생성물의 항산화성 때문으로 생각된다. 무말랭이의 환원당 및 유리아미노산 함량은 볶음 후 유의적으로 감소하였으며(p<0.05), 이에 반해 maillard 생성물의 중간산물인 5-hydroxymethyl-2-furfural(5-HMF) 함량은 무말랭이 열수 추출물에서는 검출되지 않았던 것이 가압볶음 무말랭이 열수 추출물에서는 0.57 mg/g이 측정되었다. 본 연구 결과가압볶음 무말랭이 차의 섭취는 체내 유리기에 의한 산화적손상을 보호하는 효과가 높은 것으로 사료된다.