Ingestion of Pyrrolizidine Alkaloids: A Health Hazard of Global

Oct 25, 1983 - Ingestion of Pyrrolizidine Alkaloids: A Health Hazard of Global ... Natural Products Chemistry Research, Western Regional Research Cent...
0 downloads 0 Views 3MB Size
22 Ingestion of Pyrrolizidine Alkaloids: A Health Hazard of Global Proportions JAMES N. ROITMAN

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

Natural Products Chemistry Research, Western Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, Berkeley, CA 94710 Pyrrolizidine alkaloids, about 200 of which have been identified, occur in a number of unrelated plant families distributed throughout the world. These alkaloids have been shown to be responsible for the long known hepatotoxicity in humans and animals associated with ingestion of certain plants. Because the onset of symptoms often occurs only after considerable time has elapsed (up to several years), it is likely that many, if not most, cases of pyrrolizidine alkaloid-caused liver damage are ascribed to other causes. The diverse physiological effects as well as the underlying mode of toxicity are presented. The chemical properties and analytical methods employed are summarized and the manner in which pyrrolizidine alkaloids enter the human food chain via contaminated foodstuff and the use of herbs is discussed as well as the nature of the problem in the U.S. today. Reasons for increasing consumption of herbal teas are suggested. I t was eighty years ago that G i l r u t h demonstrated by feeding experiments that tansy ragwort (Senecio jacobaea) was r e s p o n s i b l e f o r a disease o f horses and c a t t l e i n New Zealand c a l l e d Winton d i sease ( 1 ) . Other feeding experiments e s t a b l i s h e d that c e r t a i n species o f Senecio (Compositae) were r e s p o n s i b l e f o r P i c t o u d i sease of c a t t l e (Canada, 1906) ( 2 ) , Molteno disease (Cape Colony, South A f r i c a , 1904) ( 3 ) , "dunsiekte" disease of horses (South A f r i c a , 1918) ( 4 ) , and "walking d i s e a s e " of horses (northwestern Nebraska, 1929) ( 5 ) . Feeding experiments with various species of C r o t a l a r i a (Leguminosae) established the e t i o l o g y of s e v e r a l diseases of horses e x h i b i t i n g symptoms s i m i l a r to those caused by Senecio although the genera are u n r e l a t e d b o t a n i c a l l y . Diseases known as " j a a g s i e k t e " i n S. A f r i c a and "walkabout" i n A u s t r a l i a This chapter not subject to U . S . copyright. P u b l i s h e d 1983, A m e r i c a n C h e m i c a l S o c i e t y

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

346

XENOBIOTICS IN FOODS A N D F E E D S

were reproduced by feeding horses C r o t a l a r i a dura and C. retusa r e s p e c t i v e l y 06,^). A number of p l a n t s i n the f a m i l y Boraginaceae were a l s o demonstrated to cause assorted r e l a t e d diseases: H e l i o tropium species were r e s p o n s i b l e f o r l i v e r dystrophy prevalent i n c e n t r a l A s i a during the period 1931-45 i n man and domestic animals (8-12) as w e l l as sheep poisoning i n A u s t r a l i a (13); Trichodesma incanum was r e s p o n s i b l e f o r an A s i a n disease of horses and c a t t l e , c a l l e d " s u i l j u k " (14), Echium l y c o p s i s caused sheep poisoning i n A u s t r a l i a (13,15), and Amsinckia intermedia produced c i r r h o s i s i n horses and "hard l i v e r d i s e a s e " i n c a t t l e and pigs i n the P a c i f i c Northwest of the U.S. (16). Although the p l a n t s a s s o c i a t e d with these v a r i o u s , o f t e n l e t h a l , diseases occur i n three unrelated plant f a m i l i e s , a common feature of a l l i s t h e i r production of p y r r o l i z i d i n e a l k a l o i d s . These have been shown to be capable of causing the p h y s i o l o g i c a l changes c h a r a c t e r i s t i c of the abovementioned diseases although other p l a n t c o n s t i t u e n t s may play a r o l e i n exacerbating or mediating the e f f e c t s of the a l k a l o i d s and may i n part e x p l a i n some of the i n c o n s i s t e n c i e s observed i n animal feeding experiments. Chemistry of P y r r o l i z i d i n e A l k a l o i d s There are c u r r e n t l y about 200 p y r r o l i z i d i n e a l k a l o i d s known, most of which are mono- and d i - e s t e r s of the saturated and 1,2unsaturated amino-aleohoIs (commonly known as necines or necine bases) shown i n Figure 1 (17a). Numerous t o x i c o l o g i c a l s t u d i e s on small l a b o r a t o r y animals have shown that acute and chronic t o x i c i t y are caused only by e s t e r i f i e d 1,2-unsaturated necines although an unrelated per-acute syndrome, manifested by r a p i d m o r t a l i t y , can be induced by very l a r g e doses of saturated necine e s t e r s (17b,18). The s t r u c t u r e s of some r e p r e s e n t a t i v e p y r r o l i z i d i n e a l k a l o i d s are shown i n Figures 2 thru 4. The e s t e r i f y i n g a c i d s are h i g h l y branched and i n f r e q u e n t l y found elsewhere i n nature. Although the s t r u c t u r e s are not e s p e c i a l l y complex, the number of asymmetric centers renders unequivocal s t r u c t u r e d e t e r mination d i f f i c u l t . Furthermore, mixtures of diastereomers and geometric isomers o f t e n c o e x i s t i n p l a n t e x t r a c t s , and separation of these i s laborious and involves s p e c i a l techniques. These problems confounded a number of the e a r l y chemical i n v e s t i g a t i o n s e s p e c i a l l y s i n c e mixtures of the a l k a l o i d s o f t e n c r y s t a l l i z e as i f they were s i n g l e substances. An a d d i t i o n a l feature of p y r r o l i z i d i n e a l k a l o i d s i s that they o f t e n occur admixed with t h e i r N-oxides. The l a t t e r are h i g h l y water s o l u b l e and consequently are not extracted from aqueous s o l u t i o n s by the normal e x t r a c t i o n procedures employed to i s o l a t e a l k a l o i d s . However t o t a l p l a n t a l k a l o i d s may be 90% i n the form of N-oxides, rendering meaningless any estimates of a l k a l o i d content determined by normal e x t r a c t i o n techniques. Chemical reducing agents added during i s o l a t i o n procedures r a p i d l y convert Noxides to the corresponding a l k a l o i d bases allowing i s o l a t i o n from aqueous a l k a l i n e s o l u t i o n by solvent e x t r a c t i o n (17c).

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

ROiTMAN

HO

u

Ingestion

of Pyrrolizidine

Alkaloids

CHjOH

CH OH 2

CD

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

CD HELIOTRIDINE

RETRONECINE

HO

CH OH 2

H

SUPINIDINE

CH OH

H

2

°

y

^ 2°H H

Ct> CD

CH,

LINDELOFIDINE (3 OTHER STEREOISOMERS

OTONECINE

PLATYNECINE

ALSO OCCUR NATURALLY)

HO

y

CH OH 2

ct> DIHYDROXY HELIOTRIDANE

HO

H

CH OH 2

ct> ROSMARINECINE

Figure 1. Structures of necine bases, esters of which are hepatotoxic (retrone cine, heliotridine, supinidine, otonecine) or nonhepatotoxic (platynecine, dihy droxyheliotridane, rosmarinecine, lindelofidine) pyrrolizidine alkaloids.

American Chemical Society Library 1155

16th St. N. w.

Finley and Schwass; Xenobiotics Foods and Feeds Washington, D. C. in 20036 ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

XENOBIOTICS IN F O O D S A N D F E E D S

19

\ 2 0

\ ^

15

f

18

C = C - C H - C —C«'..CH "CO C H 16ÇO !7Q CH 0 2

2 1

2

co

3

3

v

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

C= C-CH -C—C""CH / CH ι I ÇH 0 ο

3

2

3

^*·ι-

0-COCH

Ç-CH -C—C""CH 2

co

/

C H — C » Q.

3

2

ho

co

i î î * CH,

3

FLORIDANINE 9. Secopyrrolizidine

OH

3

^-CH -C—C«»«

3

ί 2 Γ"

Figure

CH H

3

co

CH

C H

Ç - C H - C — C . •••CH*

CO

3

^ .

3

3

OTOSENINE alkaloids

isolated

from

life root plant

(Senecio au-

reus).

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

3

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

370

XENOBIOTICS

IN F O O D S A N D F E E D S

Comfrey* Comfrey (Symphytum spp*) has been used since the time of the Greeks f o r a great number of m e d i c i n a l purposes (117b, 122a) * One of the most prominent uses has been to promote h e a l i n g of broken bones and reduce s w e l l i n g ; t h i s e f f e c t has been documented and i s apparently caused by the a l l a n t o i n present. The a c t i o n of a l l a n t o i n may a l s o e x p l a i n the p o p u l a r i t y of comfrey as a treatment f o r bleeding of many s o r t s , both e x t e r n a l and i n t e r n a l (stomach, lungs, bowels)* Because i t contains a l a r g e amount of mucilage, i t has been used o f t e n f o r i n t e s t i n a l problems ( d i a r r h e a , dysentery) as an emollient* A d d i t i o n a l uses have been as a demulcent and expectorant f o r colds and coughs* The herb, both root and l e a f , remain popular and are o f t e n i n c l u d e d as components of the numerous h e r b a l mixtures s o l d today. Comfrey appears to have assumed the a t t r i b u t e s of a panacea. A single modern h e r b a l book (123), s o l d commonly i n h e a l t h food s t o r e s , recommends the use of comfrey to a l l e v i a t e some 47 ailments ( i n c l u d i n g a l l e r g i e s , anemia, emphysema, and diabetes) and a f f e c t ed body organs ( i n c l u d i n g bladder, lungs, kidneys, and pancreas). A number of recent studies of the p y r r o l i z i d i n e a l k a l o i d s i n v a r i o u s Symphytum species have succeeded i n c h a r a c t e r i z i n g twelve mono- and d i - e s t e r a l k a l o i d s of retronecine and h e l i o t r i d i n e (31, 95-104). We have examined twelve samples each of comfrey root and l e a f s o l d as herbs i n the U.S. As determined by nmr, the t o t a l a l k a l o i d content of the l e a f samples was < 0.005%; the r o o t s , on the other hand, contained from 0.14-0.42% (130). Examination of the r o o t a l k a l o i d mixture by c a p i l l a r y gc-ms a f t e r d e r i v a t i z a t i o n allowed i d e n t i f i c a t i o n of seven a l k a l o i d s (Figures 4 and 7); i n a l l of the samples the f i r s t four peaks, lycopsamine, intermedine, and t h e i r 7-acetyl d e r i v a t i v e s , accounted f o r 75% or more of the total alkaloids. The same seven a l k a l o i d s have been found i n Russian comfrey, a cross between Symphytum o f f i c i n a l e and S^. asperum, sometimes c a l l e d Symphytum X uplandicum (31,96,104). An aqueous i n f u s i o n of one of the comfrey root samples was prepared according to the package's d i r e c t i o n s and the aqueous s o l u t i o n was analyzed f o r a l k a l o i d by nmr a f t e r separation from the mucilage by c e n t r i f u g a t i o n , and e x t r a c t i v e workup. Of the t o t a l a l k a l o i d content of the p a r t i c u l a r sample, one t h i r d (8 mg) was i n the supernatant l i q u i d , while the remainder (17 mg) stayed i n the mucilage. However i n a c t u a l p r a c t i c e the e n t i r e sample would probably be consumed i n order to b e n e f i t from the therapeut i c p r o p e r t i e s of the mucilage. In t h i s case the a l k a l o i d s consumed per cup of tea would range between 12 mg and 36 mg depending on the amount of a l k a l o i d i n the p a r t i c u l a r r o o t sample (130). Coltsfoot. Coltsfoot (Tussilago f a r f a r a ) , known s i n c e Roman times, has been used widely f o r treatment of assorted lung and breathing ailments i n c l u d i n g asthma, b r o n c h i t i s , and coughing (117c,122b). More r e c e n t l y an examination of t h i s herb f o r a l k a l o i d s was made and the seco p y r r o l i z i d i n e , s e n k i r k i n e ( f i g u r e 3 ) , was found (105,106). We have examined s e v e r a l samples obtained l o c a l l y and" a l s o found small amounts of senkirkine ( c a . 0.004%).

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

22.

ROiTMAN

Ingestion

of Pyrrolizidine

371

Alkaloids

Borage. Borage (Borago o f f i c i n a l i s ) , another herb with a h i s t o r y of use dating back to a n c i e n t times, has been used more r e c e n t l y as a demulcent i n the treatment of v a r i o u s pulmonary complaints and as a d i u r e t i c (117d,122c). We have made a p r e l i m i n a r y examin a t i o n of a l o c a l l y - p u r c h a s e d sample of borage tea and showed the presence of p y r r o l i z i d i n e a l k a l o i d s by t i c although i n very small amounts. Examination of the crude a l k a l o i d s by c a p i l l a r y gc a f t e r d e r i v a t i z a t i o n showed only two major peaks which had r e t e n t i o n times i d e n t i c a l to two peaks found i n comfrey root, namely l y c o p s amine and 7-acetyl-lycopsamine, and suggests that these are the major a l k a l o i d s of borage. The foregoing examples make i t c l e a r that some herbs s o l d i n the U.S. do c o n t a i n p y r r o l i z i d i n e a l k a l o i d s ; others w i l l doubtless be found e s p e c i a l l y i f the herbals of various ethnic groups are examined. Why

i s the Use of Herbal Teas Increasing i n the

U.S.?

For a v a r i e t y of reasons the use of h e r b a l teas as medicine i s i n c r e a s i n g i n the U.S. a t the same time that t r a d i t i o n a l medic a l p r a c t i c e has abandoned them. I t i s perhaps s u r p r i s i n g that much of the increase has come not from those c l o s e - k n i t ethnic communities of recent immigrants where t r a d i t i o n a l use of herbs i s w e l l e s t a b l i s h e d , but l a r g e l y from the mainstream of s o c i e t y . With the exception of the ethnic "gordolobo yerba", the herbs l i s t e d i n Table I I I are g e n e r a l l y a v a i l a b l e throughout the count r y ; they are to be found a t most h e a l t h food establishments as w e l l as s p e c i a l herb shops. These establishments are f i n d i n g i n c r e a s i n g a c c e p t i b i l i t y and are as l i k e l y to be found i n suburban shopping centers as anywhere e l s e . What accounts f o r t h i s new p o p u l a r i t y of h e r b a l medicine among segments of the p o p u l a t i o n who themselves had no h i s t o r y or t r a d i t i o n of h e r b a l medicine? The explanations which f o l l o w are my own and are merely speculative. During the l a s t decade or two the word "chemical" has acquired a p e r j o r a t i v e mantle and i n the minds of many people i s equated with " t o x i c " , "unhealthy", and "unnatural". On the cont r a r y "nature" i s perceived as "safe", "wholesome", and " n a t u r a l " . P l a n t s as p a r t of "nature" of course possess i t s b e n e f i c i a l a t t r i butes; and pharmaceutical drugs, s i n c e they are "chemicals", are "bad f o r you." Second, h e r b a l medicine has a very long h i s t o r y and t r a d i t i o n . I t was, a f t e r a l l , the only form of medicine a v a i l a b l e u n t i l r a t h e r r e c e n t l y , and although i t s use has a l l but disappeared from modern medical p r a c t i c e i t remains an important source of therapy i n many areas of the world where the b e n e f i t s of modern medicine are simply u n a v a i l a b l e or u n a f f o r d a b l e . The use of h e r b a l medicine has a weighty and lengthy t r a d i t i o n and i s seen

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

XENOBIOTICS IN FOODS AND FEEDS

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

372

by some as the "Wisdom of the Ages"; i n f a c t the o r i g i n s of most f o l k remedies l i e as much i n sorcery, magic, and other i r r a t i o n a l i t i e s as i n keen e m p i r i c a l observation. A t h i r d reason to use herbal medicine i s cost; v i s i t s to p h y s i c i a n s , i n c l u d i n g t e s t s , p o s s i b l e h o s p i t a l i z a t i o n and medicat i o n are expensive, whereas s e l f - d i a g n o s i s followed by herbal medi c i n e c o s t s almost nothing. Diagnosis and treatment are r e a d i l y accomplished by purchase of any of a number of books stocked by s t o r e s s e l l i n g herb teas. These range from extensive h i s t o r i c a l treatments to l i s t s of ailments and the herbs to take f o r them accompanied by e n t h u s i a s t i c endorsements which o f t e n border on f a n a t i c i s m (117,122,123,131). Fourth there are those i n d i v i d u a l s who have a v a i l e d themselves of modern medicine, have been informed that no e f f e c t i v e cure e x i s t s and then turn to unconventional methods of which h e r b a l medicine i s only one f a c e t . F i n a l l y the f a c t that h e r b a l medicine i s , m e d i c a l l y speaking, decidedly anti-establishment may provide an i r r e s i s t i b l e a t t r a c t i o n to many counterculture enthusiasts. The U.S. Government has e s t a b l i s h e d s t r i n g e n t requirements to ensure the s a f e t y of food and drugs consumed i n the U.S. However because of p e c u l i a r i t i e s i n the r e g u l a t i o n s , herbs are not considered as food or drugs and need not be proven safe or e f f e c t i v e . The f a c t that herbs may c o n t a i n t o x i c substances such as p y r r o l i z i d i n e a l k a l o i d s has caused concern about the e f f e c t s on an everwidening group of users. Because the e f f e c t s of small repeated doses of p y r r o l i z i d i n e a l k a l o i d s i n humans are p r e s e n t l y unknown, i t would seem wise to discourage the use of herbs i n which they occur u n t i l they can be demonstrated to be s a f e . At the very l e a s t warning l a b e l s o u t l i n i n g the r i s k s ought to accompany the herbs s o l d l n r e t a i l establishments. Conclusions Because the p y r r o l i z i d i n e a l k a l o i d s are d i s t r i b u t e d i n p l a n t s growing throughout the world and t h e i r t o x i c e f f e c t s on l i v e s t o c k and man have been documented since the turn of the 20th century, many s c i e n t i s t s worldwide have s t u d i e d them. Through considerable e f f o r t , both chemical and b i o l o g i c a l , the b a s i c features of the t o x i c a c t i o n have been determined. There remain however many unanswered questions. The r e l a t i v e s e n s i t i v i t y to and p a t h o l o g i c a l e f f e c t s of the p y r r o l i z i d i n e s are very much dependent on the animal species i n v o l v e d . Even w i t h i n a s i n g l e species such as the r a t (the animal most studied) the p h y s i o l o g i c a l response i s very dose and time dependent. No s a t i s f a c t o r y explanation has been advanced to account f o r the observation of hepatic venoo c c l u s i o n i n c e r t a i n instances, hepatic megalocytosis i n others, and e n d o t h e l i a l lung l e s i o n s with (or without) l i v e r damage i n y e t o t h e r s . The considerable delay between c e s s a t i o n of a l k a l o i d a d m i n i s t r a t i o n and the onset of p a t h o l o g i c a l l y observable e f f e c t s

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

22.

ROITMAN

Ingestion

of Pyrrolizidine

Alkaloids

373

when small amounts of a l k a l o i d s are involved remains a b a f f l i n g puzzle* The r o l e played by a l k a l o i d N-oxides when ingested i s unknown except i n r a t s (where they pass i n t o the gut, are reduced t h e r e i n to a l k a l o i d s by i n t e s t i n a l m i c r o f l o r a , and are absorbed i n t o the bloodstream) and sheep (where rumenal m i c r o f l o r a reduce them to alkaloids)* I f no reducing system i s present N-oxides will probably e x h i b i t no t o x i c i t y and be excreted unchanged* The f a t e of N-oxides i n other animal species should be studied because p l a n t s can contain t h e i r p y r r o l i z i d i n e a l k a l o i d s l a r g e l y as Noxides and the r a t i o of f r e e a l k a l o i d s to N-oxides can vary g r e a t l y during the p l a n t ' s d i f f e r e n t phases of growth. The f i n d ­ ing that i n d i c i n e N-oxide administered intravenously to human cancer p a t i e n t s can cause l i v e r damage i n d i c a t e s that N-oxides are capable of e x h i b i t i n g t o x i c i t y e v i d e n t l y v i a an unknown reduc­ t i o n process somewhere i n the body. Much more b i o l o g i c a l t e s t i n g of i n d i v i d u a l a l k a l o i d s i s necessary before the e f f e c t s of subtle changes i n the s t r u c t u r e s of the a l k a l o i d s can be appraised. L i t t l e i s known of the e f f e c t s of the seco a l k a l o i d s although they comprise about one t h i r d of the known 1,2-unsaturated a l k a l o i d s . The r o l e played by c h l o r o h y d r i n and epoxide groups found i n the s i d e chains of a number of the macrocyclic dies t e r a l k a l o i d s i s unknown. I t i s hoped that Increased awareness of the nature of p y r r o l i z i d i n e t o x i c i t y and the p l a n t s that are r e s p o n s i b l e w i l l reduce the number of poisoning epidemics which occur i n T h i r d World nations and that increased v i g i l a n c e w i l l prevent p y r r o l i z i d i n e a l k a l o i d s from entering food i n the r e s t of the world. I t i s a l s o hoped that awareness or r e g u l a t i o n w i l l end the p o t e n t i a l l y dangerous i n g e s t i o n of small repeated doses of the a l k a l o i d s found i n some herbal teas. F i n a l l y the use of i n d i c i n e N-oxide as a chemotherapeutic agent i n d i c a t e s that p y r r o l i z i d i n e a l k a l o i d s ( o r s y n t h e t i c analogs) may possess u s e f u l as w e l l as t o x i c p r o p e r t i e s and may be able to a i d man as w e l l as poison him.

Literature Cited 1.

Gilruth, J.Α., 11th Ann. Rep. Dept. Αgr., N.Z. Div. Vet. Sci., 1903, 228. 2. Pethick, W.H., Rept. Vet. Director General Dep. Agr. for 1905, Can., 1906, 90. 3. Chase, W.H., Agr. J. Cape Good Hope, 1904, 25, 675. 4. Robertson, W., J. Comp. Pathol. Therap., 1906, 19, 97. 5. Van Es, L . , Cantwell, L.R., Martin, H.M., and Kramer, J., Agr. Exptl. Station Res. Bull. 43, College Agr., Univ. Nebraska, 1929. 6. Theiler, Α., 7th and 8th Rept. Dir. Vet. Res., Union S. Afri­ ca, 1918, 59. 7. Rose, A.L., Gardner, C.A., McConnell, J.D., and Bull, L.B., Aust. Vet. J., 1957, 33, 25 and 49.

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

374

XENOBIOTICS IN FOODS AND FEEDS

8. Bourkser, G.V., Rept. All Union Acad. Agr. Sci. No. 12, 1948, 44. 9. Ismaelov, N., Klin. Med. (Mosk.), 1948, 26, 23. 10. Savvina, K.I., Arkh. Patol., 1952, 14, 65. 11. Braginskii, B.M., and Bobokhodzaev, I., Sov. Med. 1965, 28, 57. 12. Braginskii, B.M., and Bobokhodzaev, I., Klin. Med., 1965, 1, 42. Excerpta Med. Sect. 4. Med. Microbiol. Immunol. Serol., 1965, 19, 1231, abstr. no. 4917. 13. Bull, L.B., Dick, A.T., Keast, J.C., and Edgar, G., Aust. J. Agric. Res., 1956, 7, 281. 14. Smirnov, F.E., and Stoljarova, A.G., Uzbeksk. Inst. Vet. Sb. Nauchn. Tr., 1959, 13, 173. 15. St. George-Grambauer, T.D., and Rac, R., Aust. Vet. J., 1962, 38, 288. 16. McCulloch, E.C., J. Am. Vet. Med. Assoc., 1940, 96, 5. 17. Bull, L.B., Culvenor, C.C.J., and Dick, A.T., "The Pyrrolizi­ dine Alkaloids"; North Holland Publishing Co.: Amsterdam, 1968; a) p 70; b) p 141; c) p 25; d) p 219; e) p 168; f) p 171; g) p 144. 18. Mc Lean, Ε.K., Pharmacol. Rev., 1970, 22, 429. 19. Mattocks, A.R., Anal. Chem., 1967, 39, 443. 20. Mattocks, A.R., Anal. Chem., 1968, 40, 1749. 21. Molyneux, R.J., and Roitman, J.N., J. Chromatogr., 1980, 21, 429. 22. Molyneux, R.J., Johnson, A.E., Roitman, J.N., and Benson, M.E., J. Agric. Food Chem., 1979, 27, 494. 23. Ramsdall, H.S., and Buhler, D.R., J. Chromatogr. 1981, 210, 154. 24. Tittel, G., Hinz, H., and Wagner, H., Planta Med., 1979, 37, 1. 25. Qualls, C.W., Jr., and Segall, H.J., J. Chromatogr., 1978, 150, 202. 26. Segall, H.J., J. Liq. Chromatogr., 1979, 2, 1319. 27. Dimenna, G.P., Krick, T.P., and Segall, H.J., J. Chromatogr., 1980, 192, 474. 28. Chalmers, A.H., Culvenor, C.C.J., and Smith, L.W., J. Chromatogr., 1965, 20, 270. 29. Deinzer, M., Thomson, P., Griffin, D., and Dickerson, E . , Biomed. Mass Spectrom., 1978, 5, 175. 30. Culvenor, C.C.J., O'Donovan, G.M., and Smith, L.W., Aust. J. Chem., 1967, 20, 801. 31. Culvenor, C.C.J., Edgar, J.Α., Frahn, J . L . , and Smith, L.W., Aust. J. Chem., 1980, 33, 1105. 32. Neuner-Jehle, N., Nesvadba, H., and Spiteller, G., Monatsh. Chem., 1965, 96, 321. 33. Pedersen, E . , and Larsen, E . , Org. Mass Spectrom., 1970, 4, 249. 34. Rashkes, Ya, V., Abdullaev, V.A., and Yunosov, S. Yu., Khim. Prir. Soedin., 1978, 153.

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

22.

ROITMAN

Ingestion

of Pyrrolizidine

Alkaloids

375

35. Mattocks, A.R., in "Phytochemical Ecology"; Harborne, J.B., Ed., Academic Press: New York, 1972. 36. Hooper, P.T., in "Effects of Poisonous Plants on Livestock"; Keeler, R., Van Kampen, K, James, L . , Eds., Academic Press: New York, 1978; p. 161. 37. Lanigan, J.W., J. Gen. Microbiol., 1976, 94, 1. 38. Huxtable, R., Paplanus, S., and Laugharn, J., Chest, 1977, 715, 308. 39. Allen, J.R., and Chesney, C.F., Exp. Mol. Pathol., 1972, 17, 220. 40. Huxtable, R.J., Ciaramitaro, D., and Eisenstein, D., Mol. Pharmacol., 1978, 14, 1189. 41. Culvenor, C.C.J., and Jago, M.V., in "Chemical Carcinogens and DNA", Vol. 1; Grover, P., Ed., CRC Press: Boca Raton, 1979; p. 161. 42. Peterson, J.E., Samuel, Α., and Jago, M.V., J. Pathol., 1972 107, 175. 43. Lewis, J.C., Rep. N.T. Vet. Stock Dep., 1912, 1912, 133. 44. Hooper, P.T., and Scanlan, W.A., Aust. Vet. J., 1977, 53, 109. 45. Sundareson, A.E., J. Pathol. Bacteriol., 1942, 54, 289. 46. Bhattacharyya, K., J. Pathol. Bacteriol., 1965, 90, 151. 47. Persand, T.V.N., and Hoyte, D.Α.Ν., Exp. Pathol. 1974, 9, 59. 48. Green, C.R., and Christie, G.S., Br. J. Exp. Pathol., 1961, 42, 369. 49. Newberne, P.M., Cancer Res., 1968, 28, 2327. 50. Armstrong, S.J., Zucherman, A.J., and Bird, R.G., Br. J. Exp. Pathol., 1971, 53, 145. 51. Martin, P.Α., Thorburn, M.J., Hutchinson, S., Bras, G., and Miller, C.G., Br. J. Exp. Pathol., 1972, 53, 374. 52. Culvenor, C.C.J., J. Pharm. Sci., 1968, 57, 1112. 53. Kupchan, S.M., and Suffness, M.I., J. Pharm. Sci., 1967, 56, 541. 54. Kugelman, Μ., Liu, W.C., Axelrod, M., McBride, T.J., and Rao, K.V., Lloydia, 1976, 39, 125. 55. Ames, M., Division of Developmental Oncology Research, Mayo Clinic; personal communication. 56. Culvenor, C.C.J., Dann, A.T., and Dick, A. T., Nature, 1962, 195, 570. 57. Holland, H.L., in "The Alkaloids, Chemistry and Physiology"; Rodrigo, R., Ed; Vol. 18, Academic Press: New York, 1981; p. 376. 58. Mattocks, A.R., Chem. Biol. Interactions, 1981, 35, 301. 59. Mattocks, A.R., J. Chem. Soc., 1969, 1155. 60. Culvenor, C.C.J., Downing, D. T., Edgar, J.Α., and Jago, M.V., Ann. N.Y. Acad. Sci., 1969, 168, 837. 61. Mattocks, A.R., Xenobiotica, 1971, 1, 563. 62. Mattocks, A.R., in "Effects of Poisonous Plants on Live­ stock"; Keeler, R.F., Van Kampen, K.R., James, L.F., Eds., Academic Press: New York, 1978; p. 177.

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

376

XENOBIOTICS IN FOODS AND FEEDS

63. Hsu, I.C., Chesney, C.F., and Allen, J.R., Proc. Soc. Exp. Biol. Med., 1973, 142, 1133. 64. Butler, W.H., Mattocks, A.R., and Barnes, J.M., J. Pathol. Bacteriol., 1970, 100, 169. 65. Lalich, J.J., Johnson, W.D., Raczniak, T.J., and Shumaker, R.C., Arch. Path. Lab. Med., 1977, 101, 69. 66. Hsu, I.C., Allen, J.R., and Chesney, C.F., Proc. Soc. Exp. Biol. Med., 1973, 144, 834. 67. Allen, J.R., and Hsu, I.C., Proc. Soc. Exp. Biol. Med., 1974, 147, 546. 68. Shumaker, R.C., Robertson, K.A., Hsu, I.C., and Allen, J.R., J. Natl. Cancer Inst., 1976, 56, 787. 69. Johnson, W.D., Robertson, K.A., Pounds, J.C., and Allen, J.R., J. Nat. Cancer Inst., 1978, 61, 85. 70. Culvenor, C.C.J., Edgar, J.Α., Jago, M.V., Outeridge, Α., Peterson, J.E., and Smith, L.W., Chem. Biol. Interactions, 1976, 12, 299. 71. Schoental, R., Nature, 1970, 227, 401. 72. Willmot, F.C., and Robertson, G.W., Lancet, 1920, 2, 848. 73. Hill, K.R., Rhodes, K., Stafford, J.L., and Aub, R., West Indian Med. J., 1951, 1, 49. 74. Stirling, G.A., Bras, G., Urquhart, A.E., Arch. Dis. Child, 1962, 37, 535. 75. Bras, G., and Hill, K.R., Lancet ii, 1956, 161. 76. Bras, G., Jellife, D.B., and Stuart, K.L., Arch. Pathol., 1954, 57, 285. 77. Stuart, K.L., and Bras, G., Q. J. Med., 1957, 26, 291. 78. Bras, G., Brooks, S.E.H., and Walter, D.C., J. Pathol. Bacteriol., 1961, 82, 503. 79. Tandon, B.N., Tandon, R.K., Tandon, H.D., Narndranathan, M., and Joshi, Υ.Κ., Lancet ii, 1976, 271. 80. Mohabbat, O., Srivastava, R.N., Younos, M.S., Sediq, G.G., Merzad, Α.Α., and Aram, G.N., Lancet ii, 1976, 269. 81. McGee, J.O'D., Patrick, R.S., Wood, C.B., and Blumgart, L.H., J. Clin. Path., 1976, 29, 788. 82. Lyford, C.L., Vergara, G.G., and Moeller, D. D. Gastroenterology, 1977, 73, 349. 83. Stillman, A.E., Huxtable, R., Consroe, P., Kohnen, P., and Smith, S., Gastroenterology, 1977, 73, 349. 84. Fox, D.W., Bergeson, P.S., Jarrett, P.B., Stillman, A.E., and Huxtable, R.J., J. Pedriatrics, 1978, 93, 980. 85. Stoloff, L., personal communication. 86. Deinzer, M.L., Thomson, P.Α., Burgett, D.M., and Isaacson, D.L., Science, 1977, 195, 497. 87. Dickenson, J.O., West. Vet., 1976, 14, 11. 88. Culvenor, C.C.J., Edgar, J.Α., and Smith, L.W., J. Agric. Food Chem., 1981, 29, 958. 89. Dickenson, J.O., Cooke, M.P., King, R.P., and Mohamed, P.Α., J. Am. Vet. Med. Assoc., 1976, 169, 1192.

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

22.

ROITMAN

Ingestion

of Pyrrolizidine

Alkaloids

311

90. Dickenson, J.O., and King, R.P., in "Effects of Poisonous Plants on Livestock", Keeler, R.F., Van Kampen, K.R., James, L.F., Eds., Academic Press: New York, 1978, p. 201. 91. Smith, L.W., and Culvenor, C.C.J., J. Nat. Prod., 1981, 44, 129. 92. Barkley, T.M., in "North American Flora", Series II Part 10, Compositae, New York Botanical Garden: New York, 1978, p. 50. 93. Munz, P.A. and Keck, D.D., in "A California Flora", Univer­ sity of California Press: Berkeley, 1959, p. 552. 94. Molyneux, R.J., personal communication. 95. Delorme, P., Jay, M., and Ferry, S., Plant. Med. Phytother., 1977, 11, 5. 96. Pedersen, E . , Arch. Pharm. Chemi. Sci., 1975, 3, 55. 97. Furuya, T., and Araki, K., Chem. Pharm. Bull., 1968, 16, 2512. 98. Furuya, T., and Hikichi, M., Phytochemistry, 1971, 10, 2217. 99. Man'ko, I.V., Korotkova, M.P., Shevtsova, N.M., Rastit. Resur., 1969, 5, 508; Chem. Abstr., 1970, 72, 87175. 100. Huizing, H.J., and Malingre, T.M., J. Chromatogr., 1979, 176, 274. 101. Man'ko, I.V., Kotovskii, B.K., and Denisov, Yu. G., Rastit. Resur., 1970, 6, 409; Chem. Abstr., 1971, 74, 61608. 102. Man'ko, I.V., and Kotovskii, B.K., Zh. Obshch. Khim., 1970, 40, 2519; Chem. Abstr., 1971, 75, 1243. 103. Man'ko, I.V., Kotovskii, B.K., and Denisov, Yu. G., Rastit. Resur., 1970, 6, 582; Chem. Abstr., 1971, 74, 84023. 104. Culvenor, C.C.J., Clarke, Μ., Edgar, J.Α., Frahn, J . L . , Jago, M.V., Petersen, J . E . , and Smith, L.W., Experientia, 1980, 36, 377. 105. Culvenor, C.C.J., Edgar, J.Α., Smith, L.W., and Hirono, I., Aust. J. Chem., 1976, 29, 229. 106. Borka, L . , and Onshuus, I., Medd. Nor. Farm. Selsk., 1979, 41, 165. 107. Manske, R.H.F., Can. J. Res., Sect. B, 1939, 17, 8. 108. Culvenor, C.C.J., and Smith, L.W., Chem. Ind., 1954, 1386. 109. Adams, R., and Govindachari, T.R., J. Am. Chem. Soc., 1949, 71, 1956. 110. Manske, R.H.F., Can. J. Res.,Sect. B, 1939, 17, 1. 111. Adams, R., and Govindachari, T.R., J. Am. Chem. Soc., 1949, 71, 1180. 112. Adams, R., and Looker, J.H., J. Am. Chem. Soc., 1951, 73, 134. 113. Warren, F.L., Kropman, M., Adams, R., Govindachari, T.R., and Looker, J.H., J. Am. Chem. Soc., 1950, 72, 1421. 114. Manske, R.H.F., Can. J. Res., Sect. B, 1936, 14, 6. 115. Mills, F.D., Diss. Abstr., B, 1967, 27, 3861. 116. Lewis, W.H., and Elvin-Lewis, M.P.F., "Medical Botany, Plants Affecting Man's Health," John Wiley and Sons: New York, 1977, p. 322.

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.

Downloaded by UNIV OF PITTSBURGH on March 8, 2016 | http://pubs.acs.org Publication Date: October 25, 1983 | doi: 10.1021/bk-1983-0234.ch022

378

XENOBIOTICS IN FOODS A N D F E E D S

117. Grieve, Μ., "A Modern Herbal", Dover Publications: New York, 1971; a) p 379; b) p 215; c) p 212; d) p 119. 118. Mattocks, A.R., and White, I.N.H., Chem. Biol. Interactions, 1971, 3, 383. 119. Culvenor, C.C.J., Edgar, J.Α., Smith, L.W., Jago, M.V. and Peterson, J . E . , Nature New Biol., 1971, 229, 255. 120. Hirono, I., Mori, H., Yamada, K., Hirata, Y., Haga, M., Tetematsu, H., and Kanie, S., J. Nat. Cancer Inst., 1977, 58, 1155. 121. Schoental, R., and Cavanagh, J. Nal. Cancer Inst., 1972, 49, 665. 122. Bianchini, F., Corbetta, F., and Pistoia, Μ., "Health Plants of the World", Newsweek Books: New York, 1977; a) p 156; b) p 98; c) p 132. 123. Royal, P.C., "Herbally Yours", Biworld Publications: Provo, Utah, 1979; p 17. 124. Man'ko, I.V., Mel'kumova, Z.V., and Malysheva, V.F., Rastit. Resur., 1972, 8, 538; Chem. Abstr., 1973, 78, 82085. 125. Mel'kumova, Z.V., Telezhenetskaya, M.V., Yunosov, S. Yu, and Man'ko, I.V., Khim. Prir. Soedin., 1974, 478. 126. Ulubelen, Α., and Doganca, S., Tetrahedron Lett., 1970, 2583. 127. Ulubelen, Α., and Doganca, S., Photochemistry, 1971, 10, 441. 128. Ulubelen, Α., and Ocal, F., Phytochemistry, 1977, 16, 499. 129. Culvenor, C.C.J., Edgar, J.Α., Frahn, J . L . , Smith, L.W., Ulubelen, Α., and Doganca, S., Aust. J. Chem., 1975, 28, 173. 130. Roitman, J., Lancet ii, 1981, 944. 131. Meyers, N., "Indian Herbal Lore, Keys to Health in the Modern World"; Pamphlet, no publisher or date of publication shown. RECEIVED June

28, 1983

Finley and Schwass; Xenobiotics in Foods and Feeds ACS Symposium Series; American Chemical Society: Washington, DC, 1983.